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You searched for subject:(recombinant proteins). Showing records 1 – 30 of 258 total matches.

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Massey University

1. Du, Jinping. Design of bacterial polyester beads for recombinant protein production, biomolecule separation and detection.

Degree: PhD, Microbiology, 2018, Massey University

 Protein recovery and biomolecule detection are commonly required for scientific research as well as industrial activities. However, it is generally complicated and costly either to… (more)

Subjects/Keywords: Biopolymers; Recombinant proteins; Recombinant proteins; Purification; Biomolecules; Separation

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APA (6th Edition):

Du, J. (2018). Design of bacterial polyester beads for recombinant protein production, biomolecule separation and detection. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/15326

Chicago Manual of Style (16th Edition):

Du, Jinping. “Design of bacterial polyester beads for recombinant protein production, biomolecule separation and detection.” 2018. Doctoral Dissertation, Massey University. Accessed April 19, 2021. http://hdl.handle.net/10179/15326.

MLA Handbook (7th Edition):

Du, Jinping. “Design of bacterial polyester beads for recombinant protein production, biomolecule separation and detection.” 2018. Web. 19 Apr 2021.

Vancouver:

Du J. Design of bacterial polyester beads for recombinant protein production, biomolecule separation and detection. [Internet] [Doctoral dissertation]. Massey University; 2018. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10179/15326.

Council of Science Editors:

Du J. Design of bacterial polyester beads for recombinant protein production, biomolecule separation and detection. [Doctoral Dissertation]. Massey University; 2018. Available from: http://hdl.handle.net/10179/15326


Hong Kong University of Science and Technology

2. Thiyagarajan, Sivakumar LIFS. An efficient intein approach to improve recombinant production of basic fibroblast growth factor in escherichia coli.

Degree: 2018, Hong Kong University of Science and Technology

 Basic Fibroblast Growth Factor (bFGF) is one of the twenty two members of fibroblast growth factors family with most potent angiogenic and wound healing properties.… (more)

Subjects/Keywords: Fibroblast growth factors ; Recombinant proteins ; Recombinant DNA ; Fermentation ; Escherichia coli ; Growth

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APA (6th Edition):

Thiyagarajan, S. L. (2018). An efficient intein approach to improve recombinant production of basic fibroblast growth factor in escherichia coli. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-96197 ; https://doi.org/10.14711/thesis-991012655069703412 ; http://repository.ust.hk/ir/bitstream/1783.1-96197/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Thiyagarajan, Sivakumar LIFS. “An efficient intein approach to improve recombinant production of basic fibroblast growth factor in escherichia coli.” 2018. Thesis, Hong Kong University of Science and Technology. Accessed April 19, 2021. http://repository.ust.hk/ir/Record/1783.1-96197 ; https://doi.org/10.14711/thesis-991012655069703412 ; http://repository.ust.hk/ir/bitstream/1783.1-96197/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Thiyagarajan, Sivakumar LIFS. “An efficient intein approach to improve recombinant production of basic fibroblast growth factor in escherichia coli.” 2018. Web. 19 Apr 2021.

Vancouver:

Thiyagarajan SL. An efficient intein approach to improve recombinant production of basic fibroblast growth factor in escherichia coli. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2018. [cited 2021 Apr 19]. Available from: http://repository.ust.hk/ir/Record/1783.1-96197 ; https://doi.org/10.14711/thesis-991012655069703412 ; http://repository.ust.hk/ir/bitstream/1783.1-96197/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Thiyagarajan SL. An efficient intein approach to improve recombinant production of basic fibroblast growth factor in escherichia coli. [Thesis]. Hong Kong University of Science and Technology; 2018. Available from: http://repository.ust.hk/ir/Record/1783.1-96197 ; https://doi.org/10.14711/thesis-991012655069703412 ; http://repository.ust.hk/ir/bitstream/1783.1-96197/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

3. Obradovic, Milan 1981-. Identification of Lawsonia intracellularis proteins recognized by neutralizing antibodies and use of these proteins to design a subunit vaccine.

Degree: 2019, University of Saskatchewan

 Lawsonia intracellularis is an obligate intracellular microorganism which causes diseases known as porcine ileitis or porcine proliferative enteropathy. Due to its obligate intracellular nature, characterization… (more)

Subjects/Keywords: L. intracellularis; recombinant proteins; subunit vaccine

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APA (6th Edition):

Obradovic, M. 1. (2019). Identification of Lawsonia intracellularis proteins recognized by neutralizing antibodies and use of these proteins to design a subunit vaccine. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12117

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Obradovic, Milan 1981-. “Identification of Lawsonia intracellularis proteins recognized by neutralizing antibodies and use of these proteins to design a subunit vaccine.” 2019. Thesis, University of Saskatchewan. Accessed April 19, 2021. http://hdl.handle.net/10388/12117.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Obradovic, Milan 1981-. “Identification of Lawsonia intracellularis proteins recognized by neutralizing antibodies and use of these proteins to design a subunit vaccine.” 2019. Web. 19 Apr 2021.

Vancouver:

Obradovic M1. Identification of Lawsonia intracellularis proteins recognized by neutralizing antibodies and use of these proteins to design a subunit vaccine. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10388/12117.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Obradovic M1. Identification of Lawsonia intracellularis proteins recognized by neutralizing antibodies and use of these proteins to design a subunit vaccine. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12117

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Queensland University of Technology

4. Tan, Yu Pei. The development of Lactococcus lactis as an antimicrobial agent.

Degree: 2010, Queensland University of Technology

 Non-pathogenic lactic acid bacteria are economically important Gram-positive bacteria used extensively in the food industry. Due to their “generally regarded as safe” status, certain species… (more)

Subjects/Keywords: Lactococcus; recombinant protein secretion; lysostaphin; ECM proteins

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APA (6th Edition):

Tan, Y. P. (2010). The development of Lactococcus lactis as an antimicrobial agent. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/39143/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tan, Yu Pei. “The development of Lactococcus lactis as an antimicrobial agent.” 2010. Thesis, Queensland University of Technology. Accessed April 19, 2021. https://eprints.qut.edu.au/39143/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tan, Yu Pei. “The development of Lactococcus lactis as an antimicrobial agent.” 2010. Web. 19 Apr 2021.

Vancouver:

Tan YP. The development of Lactococcus lactis as an antimicrobial agent. [Internet] [Thesis]. Queensland University of Technology; 2010. [cited 2021 Apr 19]. Available from: https://eprints.qut.edu.au/39143/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tan YP. The development of Lactococcus lactis as an antimicrobial agent. [Thesis]. Queensland University of Technology; 2010. Available from: https://eprints.qut.edu.au/39143/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Massey University

5. Manderson, Daniel. Development of optimal fermentation expression systems for recombinant proteins: a thesis submitted in partial fulfilment of the requirements for the degree of Masters in Technology at Massey University .

Degree: 2004, Massey University

 This research set out to maximise the titre of four recombinant protein products (i.e. Eg95 vaccine antigen against Echinococcus granulosus a aspartyl protease inhibitor homologue,… (more)

Subjects/Keywords: Recombinant proteins  – Synthesis

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APA (6th Edition):

Manderson, D. (2004). Development of optimal fermentation expression systems for recombinant proteins: a thesis submitted in partial fulfilment of the requirements for the degree of Masters in Technology at Massey University . (Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/12019

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Manderson, Daniel. “Development of optimal fermentation expression systems for recombinant proteins: a thesis submitted in partial fulfilment of the requirements for the degree of Masters in Technology at Massey University .” 2004. Thesis, Massey University. Accessed April 19, 2021. http://hdl.handle.net/10179/12019.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Manderson, Daniel. “Development of optimal fermentation expression systems for recombinant proteins: a thesis submitted in partial fulfilment of the requirements for the degree of Masters in Technology at Massey University .” 2004. Web. 19 Apr 2021.

Vancouver:

Manderson D. Development of optimal fermentation expression systems for recombinant proteins: a thesis submitted in partial fulfilment of the requirements for the degree of Masters in Technology at Massey University . [Internet] [Thesis]. Massey University; 2004. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10179/12019.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Manderson D. Development of optimal fermentation expression systems for recombinant proteins: a thesis submitted in partial fulfilment of the requirements for the degree of Masters in Technology at Massey University . [Thesis]. Massey University; 2004. Available from: http://hdl.handle.net/10179/12019

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Utah State University

6. Gaztambide, Danielle A. Production and Purification of Synthetic Minor Ampullate Silk Proteins.

Degree: MS, Biological and Irrigation Engineering, 2018, Utah State University

  Spider silks are incredible natural materials that have a wide variety of properties that can rival or outperform even common synthetic materials like Nylon… (more)

Subjects/Keywords: spider silk; proteins; minor ampullate; recombinant; Engineering

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APA (6th Edition):

Gaztambide, D. A. (2018). Production and Purification of Synthetic Minor Ampullate Silk Proteins. (Masters Thesis). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/7306

Chicago Manual of Style (16th Edition):

Gaztambide, Danielle A. “Production and Purification of Synthetic Minor Ampullate Silk Proteins.” 2018. Masters Thesis, Utah State University. Accessed April 19, 2021. https://digitalcommons.usu.edu/etd/7306.

MLA Handbook (7th Edition):

Gaztambide, Danielle A. “Production and Purification of Synthetic Minor Ampullate Silk Proteins.” 2018. Web. 19 Apr 2021.

Vancouver:

Gaztambide DA. Production and Purification of Synthetic Minor Ampullate Silk Proteins. [Internet] [Masters thesis]. Utah State University; 2018. [cited 2021 Apr 19]. Available from: https://digitalcommons.usu.edu/etd/7306.

Council of Science Editors:

Gaztambide DA. Production and Purification of Synthetic Minor Ampullate Silk Proteins. [Masters Thesis]. Utah State University; 2018. Available from: https://digitalcommons.usu.edu/etd/7306


Michigan State University

7. Vogel, Erica Paige. Production, purification, quantification, and labeling of recombinant proteins and solid state nuclear magnetic resonance studies in membranes and cellular materials.

Degree: 2012, Michigan State University

Thesis Ph. D. Michigan State University. Chemistry and Quantitative Biology 2012.

Solid state nuclear magnetic resonance (SSNMR) spectroscopy provides the opportunity to obtain high resolution… (more)

Subjects/Keywords: Recombinant proteins; Nuclear magnetic resonance; Chemistry

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APA (6th Edition):

Vogel, E. P. (2012). Production, purification, quantification, and labeling of recombinant proteins and solid state nuclear magnetic resonance studies in membranes and cellular materials. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:245

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Vogel, Erica Paige. “Production, purification, quantification, and labeling of recombinant proteins and solid state nuclear magnetic resonance studies in membranes and cellular materials.” 2012. Thesis, Michigan State University. Accessed April 19, 2021. http://etd.lib.msu.edu/islandora/object/etd:245.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Vogel, Erica Paige. “Production, purification, quantification, and labeling of recombinant proteins and solid state nuclear magnetic resonance studies in membranes and cellular materials.” 2012. Web. 19 Apr 2021.

Vancouver:

Vogel EP. Production, purification, quantification, and labeling of recombinant proteins and solid state nuclear magnetic resonance studies in membranes and cellular materials. [Internet] [Thesis]. Michigan State University; 2012. [cited 2021 Apr 19]. Available from: http://etd.lib.msu.edu/islandora/object/etd:245.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Vogel EP. Production, purification, quantification, and labeling of recombinant proteins and solid state nuclear magnetic resonance studies in membranes and cellular materials. [Thesis]. Michigan State University; 2012. Available from: http://etd.lib.msu.edu/islandora/object/etd:245

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Univerzitet u Beogradu

8. Mihaljica, Darko B. 1982-. Потенцијал рекомбинантних протеина пљувачке крпеља Ixodes ricinus (Linnaeus, 1758) за детекцију специфичних антитела као маркера убода крпељa.

Degree: Biološki fakultet, 2018, Univerzitet u Beogradu

БИОЛОГИЈА - ИМУНОБИОЛОГИЈА / BIOLOGY - IMMUNOBIOLOGY

Процена изложености крпељима је значајна у епидемиолошким студијама обољења чије узрочнике преносе крпељи, а потврда убода крпеља је… (more)

Subjects/Keywords: saliva proteins; recombinant proteins; antibodies; tick bite markers; exposure to ticks

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APA (6th Edition):

Mihaljica, D. B. 1. (2018). Потенцијал рекомбинантних протеина пљувачке крпеља Ixodes ricinus (Linnaeus, 1758) за детекцију специфичних антитела као маркера убода крпељa. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:17528/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mihaljica, Darko B 1982-. “Потенцијал рекомбинантних протеина пљувачке крпеља Ixodes ricinus (Linnaeus, 1758) за детекцију специфичних антитела као маркера убода крпељa.” 2018. Thesis, Univerzitet u Beogradu. Accessed April 19, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:17528/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mihaljica, Darko B 1982-. “Потенцијал рекомбинантних протеина пљувачке крпеља Ixodes ricinus (Linnaeus, 1758) за детекцију специфичних антитела као маркера убода крпељa.” 2018. Web. 19 Apr 2021.

Vancouver:

Mihaljica DB1. Потенцијал рекомбинантних протеина пљувачке крпеља Ixodes ricinus (Linnaeus, 1758) за детекцију специфичних антитела као маркера убода крпељa. [Internet] [Thesis]. Univerzitet u Beogradu; 2018. [cited 2021 Apr 19]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:17528/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mihaljica DB1. Потенцијал рекомбинантних протеина пљувачке крпеља Ixodes ricinus (Linnaeus, 1758) за детекцију специфичних антитела као маркера убода крпељa. [Thesis]. Univerzitet u Beogradu; 2018. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:17528/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade do Rio Grande do Norte

9. Chaves, Roberta Viana Araújo. Avaliação de dois clones de Escherichia coli recombinante quanto ao crescimento e expressão de antígenos de Leishmania chagasi (kmp11 e P36) .

Degree: 2009, Universidade do Rio Grande do Norte

 Visceral leishmaniosis caused by Leishmania chagasi, also known as calazar, presented, in the period from 1990 to 2005, tax of incidence in Brazil varying between… (more)

Subjects/Keywords: Proteínas; Escherichia coli recombinante; Leishmania chagasi Antígenos recombinantes; Clones recombinantes; Proteins; Recombinant Escherichia coli; Leishmania chagasi Recombinant antigens; Recombinant clones

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APA (6th Edition):

Chaves, R. V. A. (2009). Avaliação de dois clones de Escherichia coli recombinante quanto ao crescimento e expressão de antígenos de Leishmania chagasi (kmp11 e P36) . (Thesis). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/15787

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chaves, Roberta Viana Araújo. “Avaliação de dois clones de Escherichia coli recombinante quanto ao crescimento e expressão de antígenos de Leishmania chagasi (kmp11 e P36) .” 2009. Thesis, Universidade do Rio Grande do Norte. Accessed April 19, 2021. http://repositorio.ufrn.br/handle/123456789/15787.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chaves, Roberta Viana Araújo. “Avaliação de dois clones de Escherichia coli recombinante quanto ao crescimento e expressão de antígenos de Leishmania chagasi (kmp11 e P36) .” 2009. Web. 19 Apr 2021.

Vancouver:

Chaves RVA. Avaliação de dois clones de Escherichia coli recombinante quanto ao crescimento e expressão de antígenos de Leishmania chagasi (kmp11 e P36) . [Internet] [Thesis]. Universidade do Rio Grande do Norte; 2009. [cited 2021 Apr 19]. Available from: http://repositorio.ufrn.br/handle/123456789/15787.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chaves RVA. Avaliação de dois clones de Escherichia coli recombinante quanto ao crescimento e expressão de antígenos de Leishmania chagasi (kmp11 e P36) . [Thesis]. Universidade do Rio Grande do Norte; 2009. Available from: http://repositorio.ufrn.br/handle/123456789/15787

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

10. Zahm, Jacob Aaron. Physical Studies of Actin Nucleation and Conformational Dynamics.

Degree: 2017, University of Texas Southwestern Medical Center

 Actin is a 42 kilodalton ATPase that exists ubiquitously in eukaryotic cells. Unlike other ATPases, however, actin, under suitable conditions, can polymerize, forming helical filaments.… (more)

Subjects/Keywords: Actins; Bacterial Proteins; Carbon Isotopes; Nuclear Magnetic Resonance, Biomolecular; Recombinant Proteins; Vibrio parahaemolyticus

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APA (6th Edition):

Zahm, J. A. (2017). Physical Studies of Actin Nucleation and Conformational Dynamics. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7732

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zahm, Jacob Aaron. “Physical Studies of Actin Nucleation and Conformational Dynamics.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed April 19, 2021. http://hdl.handle.net/2152.5/7732.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zahm, Jacob Aaron. “Physical Studies of Actin Nucleation and Conformational Dynamics.” 2017. Web. 19 Apr 2021.

Vancouver:

Zahm JA. Physical Studies of Actin Nucleation and Conformational Dynamics. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/2152.5/7732.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zahm JA. Physical Studies of Actin Nucleation and Conformational Dynamics. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7732

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Adelaide

11. Falconer, Robert J. Chemical extraction of recombinant protein from the cytoplasm of Escherichia coli / by Robert John Falconer.

Degree: 1997, University of Adelaide

Describes selective and nonselective procedures to extract recombinant protein from the cytoplasm of Escherichia coli. Advisors/Committee Members: Dept. of Chemical Engineering (school).

Subjects/Keywords: Recombinant proteins.; Escherichia coli.; Proteins Separation.

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APA (6th Edition):

Falconer, R. J. (1997). Chemical extraction of recombinant protein from the cytoplasm of Escherichia coli / by Robert John Falconer. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19101

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Falconer, Robert J. “Chemical extraction of recombinant protein from the cytoplasm of Escherichia coli / by Robert John Falconer.” 1997. Thesis, University of Adelaide. Accessed April 19, 2021. http://hdl.handle.net/2440/19101.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Falconer, Robert J. “Chemical extraction of recombinant protein from the cytoplasm of Escherichia coli / by Robert John Falconer.” 1997. Web. 19 Apr 2021.

Vancouver:

Falconer RJ. Chemical extraction of recombinant protein from the cytoplasm of Escherichia coli / by Robert John Falconer. [Internet] [Thesis]. University of Adelaide; 1997. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/2440/19101.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Falconer RJ. Chemical extraction of recombinant protein from the cytoplasm of Escherichia coli / by Robert John Falconer. [Thesis]. University of Adelaide; 1997. Available from: http://hdl.handle.net/2440/19101

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of California – San Diego

12. Schmidt, Emily Noelle. A Tool for Visualization of Recombinant Protein Expression in Chlamydomonas reinhardtii with a Self-Cleaving FMDV 2A Peptide.

Degree: Biology, 2017, University of California – San Diego

Recombinant proteins are widely used for industrial purposes including manufacturing, pharmaceuticals, and beauty. Using microalgae as a biomanufacturing platform has piqued research interests due to… (more)

Subjects/Keywords: Biology; algae; biotechnology; Chlamydomonas; expression vector; polycistronic; recombinant proteins

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APA (6th Edition):

Schmidt, E. N. (2017). A Tool for Visualization of Recombinant Protein Expression in Chlamydomonas reinhardtii with a Self-Cleaving FMDV 2A Peptide. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/4w4532p2

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Schmidt, Emily Noelle. “A Tool for Visualization of Recombinant Protein Expression in Chlamydomonas reinhardtii with a Self-Cleaving FMDV 2A Peptide.” 2017. Thesis, University of California – San Diego. Accessed April 19, 2021. http://www.escholarship.org/uc/item/4w4532p2.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Schmidt, Emily Noelle. “A Tool for Visualization of Recombinant Protein Expression in Chlamydomonas reinhardtii with a Self-Cleaving FMDV 2A Peptide.” 2017. Web. 19 Apr 2021.

Vancouver:

Schmidt EN. A Tool for Visualization of Recombinant Protein Expression in Chlamydomonas reinhardtii with a Self-Cleaving FMDV 2A Peptide. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2021 Apr 19]. Available from: http://www.escholarship.org/uc/item/4w4532p2.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Schmidt EN. A Tool for Visualization of Recombinant Protein Expression in Chlamydomonas reinhardtii with a Self-Cleaving FMDV 2A Peptide. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/4w4532p2

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade Federal de Mato Grosso do Sul

13. Gomes, Juliana da Silva. Produção e avaliação preliminar de uma proteína recombinante quimérica para uso no controle de Tristeza parasitária bovina (TPB) .

Degree: 2015, Universidade Federal de Mato Grosso do Sul

 A tristeza parasitária bovina é uma importante doença causada pela riquétsia Anaplasma marginale e pelos protozoários Babesia bovis e Babesia bigemina, responsáveis por consideráveis perdas… (more)

Subjects/Keywords: Anaplasma Marginale; Babesia; Vacinas; Bovinos; Proteínas Recombinantes; Vaccines; Cattle; Recombinant Proteins

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Gomes, J. d. S. (2015). Produção e avaliação preliminar de uma proteína recombinante quimérica para uso no controle de Tristeza parasitária bovina (TPB) . (Thesis). Universidade Federal de Mato Grosso do Sul. Retrieved from http://repositorio.cbc.ufms.br:8080/jspui/handle/123456789/2288

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gomes, Juliana da Silva. “Produção e avaliação preliminar de uma proteína recombinante quimérica para uso no controle de Tristeza parasitária bovina (TPB) .” 2015. Thesis, Universidade Federal de Mato Grosso do Sul. Accessed April 19, 2021. http://repositorio.cbc.ufms.br:8080/jspui/handle/123456789/2288.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gomes, Juliana da Silva. “Produção e avaliação preliminar de uma proteína recombinante quimérica para uso no controle de Tristeza parasitária bovina (TPB) .” 2015. Web. 19 Apr 2021.

Vancouver:

Gomes JdS. Produção e avaliação preliminar de uma proteína recombinante quimérica para uso no controle de Tristeza parasitária bovina (TPB) . [Internet] [Thesis]. Universidade Federal de Mato Grosso do Sul; 2015. [cited 2021 Apr 19]. Available from: http://repositorio.cbc.ufms.br:8080/jspui/handle/123456789/2288.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gomes JdS. Produção e avaliação preliminar de uma proteína recombinante quimérica para uso no controle de Tristeza parasitária bovina (TPB) . [Thesis]. Universidade Federal de Mato Grosso do Sul; 2015. Available from: http://repositorio.cbc.ufms.br:8080/jspui/handle/123456789/2288

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

14. Kim, Hyun-Eui. Biochemical Analysis of Apoptosome Formation.

Degree: 2006, University of Texas Southwestern Medical Center

 Apoptosis is an active cell death program executed by proteases named caspases. One of the major caspase-activating pathways is initiated by mitochondria. Upon various apoptotic… (more)

Subjects/Keywords: Caspases; Recombinant Proteins; Apoptosomes

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kim, H. (2006). Biochemical Analysis of Apoptosome Formation. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/380

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kim, Hyun-Eui. “Biochemical Analysis of Apoptosome Formation.” 2006. Thesis, University of Texas Southwestern Medical Center. Accessed April 19, 2021. http://hdl.handle.net/2152.5/380.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kim, Hyun-Eui. “Biochemical Analysis of Apoptosome Formation.” 2006. Web. 19 Apr 2021.

Vancouver:

Kim H. Biochemical Analysis of Apoptosome Formation. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2006. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/2152.5/380.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kim H. Biochemical Analysis of Apoptosome Formation. [Thesis]. University of Texas Southwestern Medical Center; 2006. Available from: http://hdl.handle.net/2152.5/380

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Queensland University of Technology

15. Facy, Suzanne. Investigation of highly regulated promoters for the production of recombinant proteins in plants.

Degree: 2009, Queensland University of Technology

 Plants have been identified as promising expression systems for the commercial production of recombinant proteins. Plant-based protein production or “biofarming” offers a number of advantages… (more)

Subjects/Keywords: recombinant proteins; plants; biofarming; plant-based production; transgenic plants

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APA (6th Edition):

Facy, S. (2009). Investigation of highly regulated promoters for the production of recombinant proteins in plants. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/31771/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Facy, Suzanne. “Investigation of highly regulated promoters for the production of recombinant proteins in plants.” 2009. Thesis, Queensland University of Technology. Accessed April 19, 2021. https://eprints.qut.edu.au/31771/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Facy, Suzanne. “Investigation of highly regulated promoters for the production of recombinant proteins in plants.” 2009. Web. 19 Apr 2021.

Vancouver:

Facy S. Investigation of highly regulated promoters for the production of recombinant proteins in plants. [Internet] [Thesis]. Queensland University of Technology; 2009. [cited 2021 Apr 19]. Available from: https://eprints.qut.edu.au/31771/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Facy S. Investigation of highly regulated promoters for the production of recombinant proteins in plants. [Thesis]. Queensland University of Technology; 2009. Available from: https://eprints.qut.edu.au/31771/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Adelaide

16. Kotlarski, Nicholas. Process-scale renaturation of recombinant proteins from inclusion bodies / by Nicholas Kotlarski.

Degree: 1998, University of Adelaide

 Scale-up of a biochemical process involving expression of an Insulin-like Growth Factor-I analogue (LongR3IGF-I) as inclusion bodies within the bacterium Escherichia coli has been investigated.… (more)

Subjects/Keywords: 660.63 21; Recombinant proteins Analysis.

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APA (6th Edition):

Kotlarski, N. (1998). Process-scale renaturation of recombinant proteins from inclusion bodies / by Nicholas Kotlarski. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19259

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kotlarski, Nicholas. “Process-scale renaturation of recombinant proteins from inclusion bodies / by Nicholas Kotlarski.” 1998. Thesis, University of Adelaide. Accessed April 19, 2021. http://hdl.handle.net/2440/19259.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kotlarski, Nicholas. “Process-scale renaturation of recombinant proteins from inclusion bodies / by Nicholas Kotlarski.” 1998. Web. 19 Apr 2021.

Vancouver:

Kotlarski N. Process-scale renaturation of recombinant proteins from inclusion bodies / by Nicholas Kotlarski. [Internet] [Thesis]. University of Adelaide; 1998. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/2440/19259.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kotlarski N. Process-scale renaturation of recombinant proteins from inclusion bodies / by Nicholas Kotlarski. [Thesis]. University of Adelaide; 1998. Available from: http://hdl.handle.net/2440/19259

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Oxford

17. Rossi, Merja. Investigating cell type specific metabolism using GFP as a reporter protein.

Degree: PhD, 2015, University of Oxford

 Metabolic flux analysis (MFA) is a powerful technique for quantifying the intracellular fluxes in central carbon metabolism. It relies on detection of stable isotope labelling… (more)

Subjects/Keywords: 572; Green fluorescent protein; Recombinant proteins; Arabidopsis thaliana

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APA (6th Edition):

Rossi, M. (2015). Investigating cell type specific metabolism using GFP as a reporter protein. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:0c418362-63e7-496d-9ff6-584a0c54c127 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711706

Chicago Manual of Style (16th Edition):

Rossi, Merja. “Investigating cell type specific metabolism using GFP as a reporter protein.” 2015. Doctoral Dissertation, University of Oxford. Accessed April 19, 2021. https://ora.ox.ac.uk/objects/uuid:0c418362-63e7-496d-9ff6-584a0c54c127 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711706.

MLA Handbook (7th Edition):

Rossi, Merja. “Investigating cell type specific metabolism using GFP as a reporter protein.” 2015. Web. 19 Apr 2021.

Vancouver:

Rossi M. Investigating cell type specific metabolism using GFP as a reporter protein. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2021 Apr 19]. Available from: https://ora.ox.ac.uk/objects/uuid:0c418362-63e7-496d-9ff6-584a0c54c127 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711706.

Council of Science Editors:

Rossi M. Investigating cell type specific metabolism using GFP as a reporter protein. [Doctoral Dissertation]. University of Oxford; 2015. Available from: https://ora.ox.ac.uk/objects/uuid:0c418362-63e7-496d-9ff6-584a0c54c127 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.711706


Massey University

18. Jameson, Andrew. Recombinant protein immobilisation and display by alginate.

Degree: MS, Microbiology, 2016, Massey University

 Biopolymers are a diverse group of organic materials with important applications in a number of industries. Their ability to adsorb and encapsulate compounds has been… (more)

Subjects/Keywords: Alginates; Biopolymers; Biotechnology; Recombinant proteins; Research Subject Categories::TECHNOLOGY::Bioengineering

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APA (6th Edition):

Jameson, A. (2016). Recombinant protein immobilisation and display by alginate. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/11221

Chicago Manual of Style (16th Edition):

Jameson, Andrew. “Recombinant protein immobilisation and display by alginate.” 2016. Masters Thesis, Massey University. Accessed April 19, 2021. http://hdl.handle.net/10179/11221.

MLA Handbook (7th Edition):

Jameson, Andrew. “Recombinant protein immobilisation and display by alginate.” 2016. Web. 19 Apr 2021.

Vancouver:

Jameson A. Recombinant protein immobilisation and display by alginate. [Internet] [Masters thesis]. Massey University; 2016. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10179/11221.

Council of Science Editors:

Jameson A. Recombinant protein immobilisation and display by alginate. [Masters Thesis]. Massey University; 2016. Available from: http://hdl.handle.net/10179/11221


University of Texas – Austin

19. Harvey, Barrett Rowland. Anchored periplasmic expression (APEx): a versatile technology for the flow cytometric selection of high affinity antibodies from Escherichia coli expressed libraries.

Degree: PhD, Ecology, Evolution and Behavior ; Microbiology ; Plant Biology, 2003, University of Texas – Austin

Recombinant proteins are increasingly being used in health care over a broad spectrum of applications, ranging from cancer treatment to microbial infections. Antibodies in particular… (more)

Subjects/Keywords: Recombinant proteins; Escherichia coli

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APA (6th Edition):

Harvey, B. R. (2003). Anchored periplasmic expression (APEx): a versatile technology for the flow cytometric selection of high affinity antibodies from Escherichia coli expressed libraries. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/636

Chicago Manual of Style (16th Edition):

Harvey, Barrett Rowland. “Anchored periplasmic expression (APEx): a versatile technology for the flow cytometric selection of high affinity antibodies from Escherichia coli expressed libraries.” 2003. Doctoral Dissertation, University of Texas – Austin. Accessed April 19, 2021. http://hdl.handle.net/2152/636.

MLA Handbook (7th Edition):

Harvey, Barrett Rowland. “Anchored periplasmic expression (APEx): a versatile technology for the flow cytometric selection of high affinity antibodies from Escherichia coli expressed libraries.” 2003. Web. 19 Apr 2021.

Vancouver:

Harvey BR. Anchored periplasmic expression (APEx): a versatile technology for the flow cytometric selection of high affinity antibodies from Escherichia coli expressed libraries. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2003. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/2152/636.

Council of Science Editors:

Harvey BR. Anchored periplasmic expression (APEx): a versatile technology for the flow cytometric selection of high affinity antibodies from Escherichia coli expressed libraries. [Doctoral Dissertation]. University of Texas – Austin; 2003. Available from: http://hdl.handle.net/2152/636


Utah State University

20. Jones, Justin A. Aqueous Solvation Method for Recombinant Spider Silk Proteins.

Degree: PhD, Biology, 2015, Utah State University

  Two major hurdles face the production of recombinant spider silk protein (rSSp) based materials. First, the production of sufficient quantities of rSSp has proven… (more)

Subjects/Keywords: aqueous; solvation; method; recombinant; spider; silk; proteins; Biology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Jones, J. A. (2015). Aqueous Solvation Method for Recombinant Spider Silk Proteins. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/4267

Chicago Manual of Style (16th Edition):

Jones, Justin A. “Aqueous Solvation Method for Recombinant Spider Silk Proteins.” 2015. Doctoral Dissertation, Utah State University. Accessed April 19, 2021. https://digitalcommons.usu.edu/etd/4267.

MLA Handbook (7th Edition):

Jones, Justin A. “Aqueous Solvation Method for Recombinant Spider Silk Proteins.” 2015. Web. 19 Apr 2021.

Vancouver:

Jones JA. Aqueous Solvation Method for Recombinant Spider Silk Proteins. [Internet] [Doctoral dissertation]. Utah State University; 2015. [cited 2021 Apr 19]. Available from: https://digitalcommons.usu.edu/etd/4267.

Council of Science Editors:

Jones JA. Aqueous Solvation Method for Recombinant Spider Silk Proteins. [Doctoral Dissertation]. Utah State University; 2015. Available from: https://digitalcommons.usu.edu/etd/4267


Duke University

21. Banskota, Samagya. Development of Genetically Encoded Zwitterionic Polypeptides for Drug Delivery .

Degree: 2019, Duke University

  The clinical utility of many peptide, protein and small molecule drugs is limited by their short in-vivo ¬half-life. To address this limitation, we report… (more)

Subjects/Keywords: Biomedical engineering; biomaterials; drug delivery; paclitaxel delivery; recombinant proteins

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APA (6th Edition):

Banskota, S. (2019). Development of Genetically Encoded Zwitterionic Polypeptides for Drug Delivery . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/22047

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Banskota, Samagya. “Development of Genetically Encoded Zwitterionic Polypeptides for Drug Delivery .” 2019. Thesis, Duke University. Accessed April 19, 2021. http://hdl.handle.net/10161/22047.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Banskota, Samagya. “Development of Genetically Encoded Zwitterionic Polypeptides for Drug Delivery .” 2019. Web. 19 Apr 2021.

Vancouver:

Banskota S. Development of Genetically Encoded Zwitterionic Polypeptides for Drug Delivery . [Internet] [Thesis]. Duke University; 2019. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10161/22047.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Banskota S. Development of Genetically Encoded Zwitterionic Polypeptides for Drug Delivery . [Thesis]. Duke University; 2019. Available from: http://hdl.handle.net/10161/22047

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas State University – San Marcos

22. Ruymgaart, Arnold P. Purification and biochemical characterization of FEN1: A structure specific endonuclease from Xiphophorus maculatus.

Degree: MS, Chemistry and Biochemistry, 2005, Texas State University – San Marcos

 Flap endonuclease-1 (FEN1) is a structure specific 5' endo/exonuclease involved in DNA replication and repair. Presented herein are the cloning, gene structure, recombinant expression and… (more)

Subjects/Keywords: Endonucleases; DNA repair; Recombinant proteins

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APA (6th Edition):

Ruymgaart, A. P. (2005). Purification and biochemical characterization of FEN1: A structure specific endonuclease from Xiphophorus maculatus. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/12499

Chicago Manual of Style (16th Edition):

Ruymgaart, Arnold P. “Purification and biochemical characterization of FEN1: A structure specific endonuclease from Xiphophorus maculatus.” 2005. Masters Thesis, Texas State University – San Marcos. Accessed April 19, 2021. https://digital.library.txstate.edu/handle/10877/12499.

MLA Handbook (7th Edition):

Ruymgaart, Arnold P. “Purification and biochemical characterization of FEN1: A structure specific endonuclease from Xiphophorus maculatus.” 2005. Web. 19 Apr 2021.

Vancouver:

Ruymgaart AP. Purification and biochemical characterization of FEN1: A structure specific endonuclease from Xiphophorus maculatus. [Internet] [Masters thesis]. Texas State University – San Marcos; 2005. [cited 2021 Apr 19]. Available from: https://digital.library.txstate.edu/handle/10877/12499.

Council of Science Editors:

Ruymgaart AP. Purification and biochemical characterization of FEN1: A structure specific endonuclease from Xiphophorus maculatus. [Masters Thesis]. Texas State University – San Marcos; 2005. Available from: https://digital.library.txstate.edu/handle/10877/12499


Texas State University – San Marcos

23. Maldonado, Ryan. Testing the Ability of RF-amide Neuropeptides to Promote Amyloidosis of Recombinant Human Prion Protein.

Degree: MS, Biochemistry, 2014, Texas State University – San Marcos

 Protein folding is a process in which polypeptides assume their correct conformational tertiary structure from a random coil to produce a functional protein. When the… (more)

Subjects/Keywords: Prion protein; Amyloid; Neuropeptides; Amyloidosis; Peptides; Recombinant proteins; Prions

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APA (6th Edition):

Maldonado, R. (2014). Testing the Ability of RF-amide Neuropeptides to Promote Amyloidosis of Recombinant Human Prion Protein. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/4950

Chicago Manual of Style (16th Edition):

Maldonado, Ryan. “Testing the Ability of RF-amide Neuropeptides to Promote Amyloidosis of Recombinant Human Prion Protein.” 2014. Masters Thesis, Texas State University – San Marcos. Accessed April 19, 2021. https://digital.library.txstate.edu/handle/10877/4950.

MLA Handbook (7th Edition):

Maldonado, Ryan. “Testing the Ability of RF-amide Neuropeptides to Promote Amyloidosis of Recombinant Human Prion Protein.” 2014. Web. 19 Apr 2021.

Vancouver:

Maldonado R. Testing the Ability of RF-amide Neuropeptides to Promote Amyloidosis of Recombinant Human Prion Protein. [Internet] [Masters thesis]. Texas State University – San Marcos; 2014. [cited 2021 Apr 19]. Available from: https://digital.library.txstate.edu/handle/10877/4950.

Council of Science Editors:

Maldonado R. Testing the Ability of RF-amide Neuropeptides to Promote Amyloidosis of Recombinant Human Prion Protein. [Masters Thesis]. Texas State University – San Marcos; 2014. Available from: https://digital.library.txstate.edu/handle/10877/4950


University of North Texas

24. Alodailah, Sattam Sonitan. The Generation of Recombinant Zea mays Spastin and Katanin Proteins for In Vitro Analysis.

Degree: 2017, University of North Texas

 Plant microtubules play essential roles in cell processes such as cell division, cell elongation, and organelle organization. Microtubules are arranged in highly dynamic and ordered… (more)

Subjects/Keywords: Microtubules; Spastin; katanin; cytoskeleton; Plant microtubules.; Recombinant proteins.; Corn  – Cytology.

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APA (6th Edition):

Alodailah, S. S. (2017). The Generation of Recombinant Zea mays Spastin and Katanin Proteins for In Vitro Analysis. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc1062897/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Alodailah, Sattam Sonitan. “The Generation of Recombinant Zea mays Spastin and Katanin Proteins for In Vitro Analysis.” 2017. Thesis, University of North Texas. Accessed April 19, 2021. https://digital.library.unt.edu/ark:/67531/metadc1062897/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Alodailah, Sattam Sonitan. “The Generation of Recombinant Zea mays Spastin and Katanin Proteins for In Vitro Analysis.” 2017. Web. 19 Apr 2021.

Vancouver:

Alodailah SS. The Generation of Recombinant Zea mays Spastin and Katanin Proteins for In Vitro Analysis. [Internet] [Thesis]. University of North Texas; 2017. [cited 2021 Apr 19]. Available from: https://digital.library.unt.edu/ark:/67531/metadc1062897/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Alodailah SS. The Generation of Recombinant Zea mays Spastin and Katanin Proteins for In Vitro Analysis. [Thesis]. University of North Texas; 2017. Available from: https://digital.library.unt.edu/ark:/67531/metadc1062897/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

25. Raquel Sombra BasÃlio de Oliveira. ExpressÃo heterÃloga, caracterizaÃÃo cristalogrÃfica e anÃlise funcional de uma osmotina antifÃngica de Calotropis procera.

Degree: 2014, Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em BioquÃmica; UFC; BR

Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico

Em etapa anterior a este trabalho, uma proteÃna purificada a partir do lÃtex da planta Calotropis procera foi… (more)

Subjects/Keywords: cDNA; Cristalografia; LÃtex; ProteÃna recombinante; Crystallography; Latex; Recombinant proteins; BIOQUIMICA

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APA (6th Edition):

Oliveira, R. S. B. d. (2014). ExpressÃo heterÃloga, caracterizaÃÃo cristalogrÃfica e anÃlise funcional de uma osmotina antifÃngica de Calotropis procera. (Doctoral Dissertation). Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em BioquÃmica; UFC; BR. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13438

Chicago Manual of Style (16th Edition):

Oliveira, Raquel Sombra BasÃlio de. “ExpressÃo heterÃloga, caracterizaÃÃo cristalogrÃfica e anÃlise funcional de uma osmotina antifÃngica de Calotropis procera.” 2014. Doctoral Dissertation, Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em BioquÃmica; UFC; BR. Accessed April 19, 2021. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13438.

MLA Handbook (7th Edition):

Oliveira, Raquel Sombra BasÃlio de. “ExpressÃo heterÃloga, caracterizaÃÃo cristalogrÃfica e anÃlise funcional de uma osmotina antifÃngica de Calotropis procera.” 2014. Web. 19 Apr 2021.

Vancouver:

Oliveira RSBd. ExpressÃo heterÃloga, caracterizaÃÃo cristalogrÃfica e anÃlise funcional de uma osmotina antifÃngica de Calotropis procera. [Internet] [Doctoral dissertation]. Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em BioquÃmica; UFC; BR; 2014. [cited 2021 Apr 19]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13438.

Council of Science Editors:

Oliveira RSBd. ExpressÃo heterÃloga, caracterizaÃÃo cristalogrÃfica e anÃlise funcional de uma osmotina antifÃngica de Calotropis procera. [Doctoral Dissertation]. Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em BioquÃmica; UFC; BR; 2014. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13438


University of Aberdeen

26. Knowles, Christopher. Generation of mammalian cell culture systems for the rapid and efficient production of recombinant proteins.

Degree: PhD, 2016, University of Aberdeen

 The overarching objective of this thesis was the development of an improved expression cell line for recombinant proteins, in which a transgene of interest can… (more)

Subjects/Keywords: 572; Recombinant proteins; Cell cultures; Monoclonal antibodies; Somatic cells; Genetic recombination

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APA (6th Edition):

Knowles, C. (2016). Generation of mammalian cell culture systems for the rapid and efficient production of recombinant proteins. (Doctoral Dissertation). University of Aberdeen. Retrieved from https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152769590005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715451

Chicago Manual of Style (16th Edition):

Knowles, Christopher. “Generation of mammalian cell culture systems for the rapid and efficient production of recombinant proteins.” 2016. Doctoral Dissertation, University of Aberdeen. Accessed April 19, 2021. https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152769590005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715451.

MLA Handbook (7th Edition):

Knowles, Christopher. “Generation of mammalian cell culture systems for the rapid and efficient production of recombinant proteins.” 2016. Web. 19 Apr 2021.

Vancouver:

Knowles C. Generation of mammalian cell culture systems for the rapid and efficient production of recombinant proteins. [Internet] [Doctoral dissertation]. University of Aberdeen; 2016. [cited 2021 Apr 19]. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152769590005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715451.

Council of Science Editors:

Knowles C. Generation of mammalian cell culture systems for the rapid and efficient production of recombinant proteins. [Doctoral Dissertation]. University of Aberdeen; 2016. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152769590005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715451

27. Cristiane Tambascia Pereira. Estudos funcionais e estruturais para a caracterização da via de captação e assimilação de sulfato em Xanthomonas axonopodis pv. citri.

Degree: 2013, University of São Paulo

Em Escherichia coli, a assimilação de sulfato e sua redução a sulfeto é mediada por um transportador do tipo ABC codificado pelos genes sbpcysWUA e… (more)

Subjects/Keywords: Bioinformática; Oligonucleotídeos; Proteínas recombinantes; Xanthomonas; Bioinformatics; Oligonucleotides; Recombinant proteins; Xanthomonas

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pereira, C. T. (2013). Estudos funcionais e estruturais para a caracterização da via de captação e assimilação de sulfato em Xanthomonas axonopodis pv. citri. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-05112013-113438/

Chicago Manual of Style (16th Edition):

Pereira, Cristiane Tambascia. “Estudos funcionais e estruturais para a caracterização da via de captação e assimilação de sulfato em Xanthomonas axonopodis pv. citri.” 2013. Masters Thesis, University of São Paulo. Accessed April 19, 2021. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-05112013-113438/.

MLA Handbook (7th Edition):

Pereira, Cristiane Tambascia. “Estudos funcionais e estruturais para a caracterização da via de captação e assimilação de sulfato em Xanthomonas axonopodis pv. citri.” 2013. Web. 19 Apr 2021.

Vancouver:

Pereira CT. Estudos funcionais e estruturais para a caracterização da via de captação e assimilação de sulfato em Xanthomonas axonopodis pv. citri. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2021 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-05112013-113438/.

Council of Science Editors:

Pereira CT. Estudos funcionais e estruturais para a caracterização da via de captação e assimilação de sulfato em Xanthomonas axonopodis pv. citri. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-05112013-113438/

28. Renan Francisco Domingos. Caracterização de duas proteínas de Leptospira interrogans na patogênese da leptospirose.

Degree: 2014, University of São Paulo

O sequenciamento da L. interrogans sorovar Copenhageni e as análises bioinformáticas permitiram a identificação de candidatos vacinais e fatores de virulência. Foram selecionados dois genes,… (more)

Subjects/Keywords: Leptospira; Leptospirose; Patogênese; Proteínas recombinantes; Leptospira; Leptospirosis; Pathogenesis; Recombinant proteins

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Domingos, R. F. (2014). Caracterização de duas proteínas de Leptospira interrogans na patogênese da leptospirose. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-09122014-122906/

Chicago Manual of Style (16th Edition):

Domingos, Renan Francisco. “Caracterização de duas proteínas de Leptospira interrogans na patogênese da leptospirose.” 2014. Doctoral Dissertation, University of São Paulo. Accessed April 19, 2021. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-09122014-122906/.

MLA Handbook (7th Edition):

Domingos, Renan Francisco. “Caracterização de duas proteínas de Leptospira interrogans na patogênese da leptospirose.” 2014. Web. 19 Apr 2021.

Vancouver:

Domingos RF. Caracterização de duas proteínas de Leptospira interrogans na patogênese da leptospirose. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2021 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-09122014-122906/.

Council of Science Editors:

Domingos RF. Caracterização de duas proteínas de Leptospira interrogans na patogênese da leptospirose. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-09122014-122906/

29. Vivian Lika Hashimoto. Clonagem e expressão gênica de antígenos candidatos vacinais contra leptospirose.

Degree: 2012, University of São Paulo

A leptospirose é uma doença infecto-contagiosa que acomete os animais domésticos, silvestres e o homem, causada por bactérias do gênero Leptospira. No Brasil, a hemorragia… (more)

Subjects/Keywords: Leptospirose; Proteínas recombinantes; Vacinas; Leptospirosis; Recombinant proteins; Vaccines

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Hashimoto, V. L. (2012). Clonagem e expressão gênica de antígenos candidatos vacinais contra leptospirose. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-11062012-082558/

Chicago Manual of Style (16th Edition):

Hashimoto, Vivian Lika. “Clonagem e expressão gênica de antígenos candidatos vacinais contra leptospirose.” 2012. Doctoral Dissertation, University of São Paulo. Accessed April 19, 2021. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-11062012-082558/.

MLA Handbook (7th Edition):

Hashimoto, Vivian Lika. “Clonagem e expressão gênica de antígenos candidatos vacinais contra leptospirose.” 2012. Web. 19 Apr 2021.

Vancouver:

Hashimoto VL. Clonagem e expressão gênica de antígenos candidatos vacinais contra leptospirose. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2021 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-11062012-082558/.

Council of Science Editors:

Hashimoto VL. Clonagem e expressão gênica de antígenos candidatos vacinais contra leptospirose. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-11062012-082558/

30. Jupciana Martins Figueredo. Avaliação do papel de duas proteínas de Leptospira interrogans na patogênese da leptospirose.

Degree: 2016, University of São Paulo

Leptospirose é uma zoonose mundial que acomete várias espécies de mamíferos, incluindo humanos, causada por espécies de bactérias patogênicas do gênero Leptospira. Possui um quadro… (more)

Subjects/Keywords: Leptospira; Leptospirose; Proteínas recombinantes; Leptospira; Leptospirosis; Recombinant proteins

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Figueredo, J. M. (2016). Avaliação do papel de duas proteínas de Leptospira interrogans na patogênese da leptospirose. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-23032017-151831/

Chicago Manual of Style (16th Edition):

Figueredo, Jupciana Martins. “Avaliação do papel de duas proteínas de Leptospira interrogans na patogênese da leptospirose.” 2016. Masters Thesis, University of São Paulo. Accessed April 19, 2021. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-23032017-151831/.

MLA Handbook (7th Edition):

Figueredo, Jupciana Martins. “Avaliação do papel de duas proteínas de Leptospira interrogans na patogênese da leptospirose.” 2016. Web. 19 Apr 2021.

Vancouver:

Figueredo JM. Avaliação do papel de duas proteínas de Leptospira interrogans na patogênese da leptospirose. [Internet] [Masters thesis]. University of São Paulo; 2016. [cited 2021 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-23032017-151831/.

Council of Science Editors:

Figueredo JM. Avaliação do papel de duas proteínas de Leptospira interrogans na patogênese da leptospirose. [Masters Thesis]. University of São Paulo; 2016. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-23032017-151831/

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