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You searched for subject:( Combinatorial protein refolding). Showing records 1 – 30 of 17838 total matches.

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Cornell University

1. Kondapalli, Sowmya. Development Of Microfluidic Devices For Biopharmaceutical Production And Biotoxin Detection .

Degree: 2011, Cornell University

 In this work, we present two different applications of microfluidic control. In the first application, we have developed a microfluidic device that has the potential… (more)

Subjects/Keywords: Microfluidic devices; Combinatorial protein refolding; Biosensors for virus detection

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APA (6th Edition):

Kondapalli, S. (2011). Development Of Microfluidic Devices For Biopharmaceutical Production And Biotoxin Detection . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29486

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):

Kondapalli, Sowmya. “Development Of Microfluidic Devices For Biopharmaceutical Production And Biotoxin Detection .” 2011. Thesis, Cornell University. Accessed June 19, 2019. http://hdl.handle.net/1813/29486.

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

MLA Handbook (7th Edition):

Kondapalli, Sowmya. “Development Of Microfluidic Devices For Biopharmaceutical Production And Biotoxin Detection .” 2011. Web. 19 Jun 2019.

Vancouver:

Kondapalli S. Development Of Microfluidic Devices For Biopharmaceutical Production And Biotoxin Detection . [Internet] [Thesis]. Cornell University; 2011. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1813/29486.

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

Council of Science Editors:

Kondapalli S. Development Of Microfluidic Devices For Biopharmaceutical Production And Biotoxin Detection . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29486

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


University of Manchester

2. Gilburt, James. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.

Degree: 2016, University of Manchester

 The need to high quality therapeutic proteins has grown significantly in the past 30 years. Recombinant proteins are often produced from vectors inserted into E.… (more)

Subjects/Keywords: Protein refolding; Aggregation

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APA (6th Edition):

Gilburt, J. (2016). A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:295840

Chicago Manual of Style (16th Edition):

Gilburt, James. “A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.” 2016. Doctoral Dissertation, University of Manchester. Accessed June 19, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:295840.

MLA Handbook (7th Edition):

Gilburt, James. “A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.” 2016. Web. 19 Jun 2019.

Vancouver:

Gilburt J. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Jun 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:295840.

Council of Science Editors:

Gilburt J. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:295840


University of Manchester

3. Gilburt, James. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.

Degree: PhD, 2016, University of Manchester

 The need to high quality therapeutic proteins has grown significantly in the past 30 years. Recombinant proteins are often produced from vectors inserted into E.… (more)

Subjects/Keywords: 572; Protein refolding; Aggregation

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APA (6th Edition):

Gilburt, J. (2016). A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-folded-denatured-and-aggregated-states-during-the-refolding-of-inclusion-body-proteins(2985ec97-94e6-416d-bfd3-03e23306566f).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680030

Chicago Manual of Style (16th Edition):

Gilburt, James. “A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.” 2016. Doctoral Dissertation, University of Manchester. Accessed June 19, 2019. https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-folded-denatured-and-aggregated-states-during-the-refolding-of-inclusion-body-proteins(2985ec97-94e6-416d-bfd3-03e23306566f).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680030.

MLA Handbook (7th Edition):

Gilburt, James. “A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.” 2016. Web. 19 Jun 2019.

Vancouver:

Gilburt J. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Jun 19]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-folded-denatured-and-aggregated-states-during-the-refolding-of-inclusion-body-proteins(2985ec97-94e6-416d-bfd3-03e23306566f).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680030.

Council of Science Editors:

Gilburt J. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-folded-denatured-and-aggregated-states-during-the-refolding-of-inclusion-body-proteins(2985ec97-94e6-416d-bfd3-03e23306566f).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680030


University of Western Ontario

4. Alassuity, Ahmed. Continuous protein refolding in a liquid solid circulating fluidized bed (LSCFB) system.

Degree: 2017, University of Western Ontario

 Biotechnology has significantly contributed to the production of food, drugs, and a lot of specialty and chemical products. In addition to that, biotechnology provided and… (more)

Subjects/Keywords: Protein refolding; Circulating fluidized bed; IMAC beads; composite beads; matrix-assisted protein refolding; LSCFB; Biochemical and Biomolecular Engineering

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APA (6th Edition):

Alassuity, A. (2017). Continuous protein refolding in a liquid solid circulating fluidized bed (LSCFB) system. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4756

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):

Alassuity, Ahmed. “Continuous protein refolding in a liquid solid circulating fluidized bed (LSCFB) system.” 2017. Thesis, University of Western Ontario. Accessed June 19, 2019. https://ir.lib.uwo.ca/etd/4756.

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

MLA Handbook (7th Edition):

Alassuity, Ahmed. “Continuous protein refolding in a liquid solid circulating fluidized bed (LSCFB) system.” 2017. Web. 19 Jun 2019.

Vancouver:

Alassuity A. Continuous protein refolding in a liquid solid circulating fluidized bed (LSCFB) system. [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2019 Jun 19]. Available from: https://ir.lib.uwo.ca/etd/4756.

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

Council of Science Editors:

Alassuity A. Continuous protein refolding in a liquid solid circulating fluidized bed (LSCFB) system. [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/4756

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


University of California – Irvine

5. Yuan, Tom Zhiye. Accelerating directed evolution: self-mutating bacteriophage and controlled protein unfolding by shear-stress.

Degree: Biological Sciences, 2014, University of California – Irvine

 Proteins, large biological molecules synthesized by living organisms, serve a wide array of functions. Many proteins operate as molecular scaffolds for binding to other proteins;… (more)

Subjects/Keywords: Biochemistry; Biology; bordetella bacteriophage; directed evolution; phage display; protein engineering; protein refolding; shear stress

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APA (6th Edition):

Yuan, T. Z. (2014). Accelerating directed evolution: self-mutating bacteriophage and controlled protein unfolding by shear-stress. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/1cr2h8n7

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):

Yuan, Tom Zhiye. “Accelerating directed evolution: self-mutating bacteriophage and controlled protein unfolding by shear-stress.” 2014. Thesis, University of California – Irvine. Accessed June 19, 2019. http://www.escholarship.org/uc/item/1cr2h8n7.

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

MLA Handbook (7th Edition):

Yuan, Tom Zhiye. “Accelerating directed evolution: self-mutating bacteriophage and controlled protein unfolding by shear-stress.” 2014. Web. 19 Jun 2019.

Vancouver:

Yuan TZ. Accelerating directed evolution: self-mutating bacteriophage and controlled protein unfolding by shear-stress. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/1cr2h8n7.

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

Council of Science Editors:

Yuan TZ. Accelerating directed evolution: self-mutating bacteriophage and controlled protein unfolding by shear-stress. [Thesis]. University of California – Irvine; 2014. Available from: http://www.escholarship.org/uc/item/1cr2h8n7

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


University of Ottawa

6. Berhane, Nahom Ahferom. Antimicrobial Proteins for Human Health .

Degree: 2018, University of Ottawa

 Bacteria are one of the largest causes of human disease, with millions of deaths every year attributed to bacterial infections, and they have become more… (more)

Subjects/Keywords: Antibiotic resistance; protein purification; protein expression; refolding; biofilm; histone; OCX-32; eggshell

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APA (6th Edition):

Berhane, N. A. (2018). Antimicrobial Proteins for Human Health . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37283

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):

Berhane, Nahom Ahferom. “Antimicrobial Proteins for Human Health .” 2018. Thesis, University of Ottawa. Accessed June 19, 2019. http://hdl.handle.net/10393/37283.

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

MLA Handbook (7th Edition):

Berhane, Nahom Ahferom. “Antimicrobial Proteins for Human Health .” 2018. Web. 19 Jun 2019.

Vancouver:

Berhane NA. Antimicrobial Proteins for Human Health . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10393/37283.

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

Council of Science Editors:

Berhane NA. Antimicrobial Proteins for Human Health . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/37283

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


Linköping University

7. Halvarsson, Camilla. Substitution of disulphide bonds to hydrophobic amino acids in BACE1.

Degree: Chemistry and Biology, 2009, Linköping University

  The study and understanding of Alzheimer’s disease on protein level is fundamentally important in the search for its treatment and there is a demand… (more)

Subjects/Keywords: BACE1; disulphide bonds substitution; hydrophobic amino acids; protein purification; refolding time; Biochemistry; Biokemi

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APA (6th Edition):

Halvarsson, C. (2009). Substitution of disulphide bonds to hydrophobic amino acids in BACE1. (Thesis). Linköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-52180

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):

Halvarsson, Camilla. “Substitution of disulphide bonds to hydrophobic amino acids in BACE1.” 2009. Thesis, Linköping University. Accessed June 19, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-52180.

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

MLA Handbook (7th Edition):

Halvarsson, Camilla. “Substitution of disulphide bonds to hydrophobic amino acids in BACE1.” 2009. Web. 19 Jun 2019.

Vancouver:

Halvarsson C. Substitution of disulphide bonds to hydrophobic amino acids in BACE1. [Internet] [Thesis]. Linköping University; 2009. [cited 2019 Jun 19]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-52180.

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

Council of Science Editors:

Halvarsson C. Substitution of disulphide bonds to hydrophobic amino acids in BACE1. [Thesis]. Linköping University; 2009. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-52180

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


Jawaharlal Nehru University

8. Vani, Guttikonda Meher. Cosolvent assisted protein refolding: chymotrypsinogen as a model; -.

Degree: Biotechnology, 1996, Jawaharlal Nehru University

None

Bibliography p.123-132

Advisors/Committee Members: Bhat, Rajiv.

Subjects/Keywords: Biotechnology; chymotrypsinogen; refolding; Cosolvent assisted protein

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APA (6th Edition):

Vani, G. M. (1996). Cosolvent assisted protein refolding: chymotrypsinogen as a model; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/17700

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):

Vani, Guttikonda Meher. “Cosolvent assisted protein refolding: chymotrypsinogen as a model; -.” 1996. Thesis, Jawaharlal Nehru University. Accessed June 19, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/17700.

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

MLA Handbook (7th Edition):

Vani, Guttikonda Meher. “Cosolvent assisted protein refolding: chymotrypsinogen as a model; -.” 1996. Web. 19 Jun 2019.

Vancouver:

Vani GM. Cosolvent assisted protein refolding: chymotrypsinogen as a model; -. [Internet] [Thesis]. Jawaharlal Nehru University; 1996. [cited 2019 Jun 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/17700.

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

Council of Science Editors:

Vani GM. Cosolvent assisted protein refolding: chymotrypsinogen as a model; -. [Thesis]. Jawaharlal Nehru University; 1996. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/17700

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


Georgia State University

9. Castiblanco, Adriana P. Expression and Purification of Engineered Calcium Binding Proteins.

Degree: MS, Chemistry, 2009, Georgia State University

 Previous studies in Dr. Yang’s laboratory have established a grafting, design, and subdomain approach in order to investigate the properties behind Ca2+-binding sites located in… (more)

Subjects/Keywords: Ion exchange chromatography; Hydrophobic interaction chromatography; Protein refolding; Calcium sensing receptor; Affinity chromatography; Calmodulin; STIM1

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APA (6th Edition):

Castiblanco, A. P. (2009). Expression and Purification of Engineered Calcium Binding Proteins. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/20

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):

Castiblanco, Adriana P. “Expression and Purification of Engineered Calcium Binding Proteins.” 2009. Thesis, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_theses/20.

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

MLA Handbook (7th Edition):

Castiblanco, Adriana P. “Expression and Purification of Engineered Calcium Binding Proteins.” 2009. Web. 19 Jun 2019.

Vancouver:

Castiblanco AP. Expression and Purification of Engineered Calcium Binding Proteins. [Internet] [Thesis]. Georgia State University; 2009. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_theses/20.

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

Council of Science Editors:

Castiblanco AP. Expression and Purification of Engineered Calcium Binding Proteins. [Thesis]. Georgia State University; 2009. Available from: https://scholarworks.gsu.edu/chemistry_theses/20

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


McMaster University

10. Buzon, Beverlee D. Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain.

Degree: MSc, 2012, McMaster University

Interstrand cross-linking (ICL) damage to DNA is cytotoxic as it blocks replication and transcription. This cytotoxicity is exploited in anti-cancer therapies, but increased ICL… (more)

Subjects/Keywords: SNM1A; interstrand crosslink repair; beta-CASP; inclusion body protein refolding; nuclease; cisplatin; Biochemistry; Biochemistry

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APA (6th Edition):

Buzon, B. D. (2012). Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12675

Chicago Manual of Style (16th Edition):

Buzon, Beverlee D. “Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain.” 2012. Masters Thesis, McMaster University. Accessed June 19, 2019. http://hdl.handle.net/11375/12675.

MLA Handbook (7th Edition):

Buzon, Beverlee D. “Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain.” 2012. Web. 19 Jun 2019.

Vancouver:

Buzon BD. Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/11375/12675.

Council of Science Editors:

Buzon BD. Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12675

11. NIAN RUI. Intensification of inclusion body processing via surface refolding with chemical extraction.

Degree: 2009, National University of Singapore

Subjects/Keywords: molecular chaperone; protein refolding; chemical extraction

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

APA (6th Edition):

RUI, N. (2009). Intensification of inclusion body processing via surface refolding with chemical extraction. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/15884

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):

RUI, NIAN. “Intensification of inclusion body processing via surface refolding with chemical extraction.” 2009. Thesis, National University of Singapore. Accessed June 19, 2019. http://scholarbank.nus.edu.sg/handle/10635/15884.

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

MLA Handbook (7th Edition):

RUI, NIAN. “Intensification of inclusion body processing via surface refolding with chemical extraction.” 2009. Web. 19 Jun 2019.

Vancouver:

RUI N. Intensification of inclusion body processing via surface refolding with chemical extraction. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2019 Jun 19]. Available from: http://scholarbank.nus.edu.sg/handle/10635/15884.

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

Council of Science Editors:

RUI N. Intensification of inclusion body processing via surface refolding with chemical extraction. [Thesis]. National University of Singapore; 2009. Available from: http://scholarbank.nus.edu.sg/handle/10635/15884

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


KTH

12. Persson, Astrid. Recovery and refolding of OmpT fused with a Z-basic tag on a cation exchange solid support.

Degree: Biotechnology (BIO), 2011, KTH

Subjects/Keywords: OmpT; Zbasic; refolding; membrane protein; cation exchange chromatography.

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APA (6th Edition):

Persson, A. (2011). Recovery and refolding of OmpT fused with a Z-basic tag on a cation exchange solid support. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-49088

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):

Persson, Astrid. “Recovery and refolding of OmpT fused with a Z-basic tag on a cation exchange solid support.” 2011. Thesis, KTH. Accessed June 19, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-49088.

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

MLA Handbook (7th Edition):

Persson, Astrid. “Recovery and refolding of OmpT fused with a Z-basic tag on a cation exchange solid support.” 2011. Web. 19 Jun 2019.

Vancouver:

Persson A. Recovery and refolding of OmpT fused with a Z-basic tag on a cation exchange solid support. [Internet] [Thesis]. KTH; 2011. [cited 2019 Jun 19]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-49088.

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

Council of Science Editors:

Persson A. Recovery and refolding of OmpT fused with a Z-basic tag on a cation exchange solid support. [Thesis]. KTH; 2011. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-49088

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


Linköping University

13. Jansson, Lennie. Purification and refolding of a novel dipeptidyl peptidase III.

Degree: Chemistry, 2019, Linköping University

  There is a continuous search for novel enzymes to complement the abilities of today’s commercially available enzyme and find tailor-fit alternatives to suit the… (more)

Subjects/Keywords: dipeptidyl peptidase III; DPP III; purification; refolding; protein; Arg-Arg-2NA; Biochemistry and Molecular Biology; Biokemi och molekylärbiologi

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APA (6th Edition):

Jansson, L. (2019). Purification and refolding of a novel dipeptidyl peptidase III. (Thesis). Linköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-154013

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):

Jansson, Lennie. “Purification and refolding of a novel dipeptidyl peptidase III.” 2019. Thesis, Linköping University. Accessed June 19, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-154013.

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

MLA Handbook (7th Edition):

Jansson, Lennie. “Purification and refolding of a novel dipeptidyl peptidase III.” 2019. Web. 19 Jun 2019.

Vancouver:

Jansson L. Purification and refolding of a novel dipeptidyl peptidase III. [Internet] [Thesis]. Linköping University; 2019. [cited 2019 Jun 19]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-154013.

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

Council of Science Editors:

Jansson L. Purification and refolding of a novel dipeptidyl peptidase III. [Thesis]. Linköping University; 2019. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-154013

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

14. 佐藤, 友人. 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.

Degree: 博士(バイオサイエンス), 2015, Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学

2014

Subjects/Keywords: Measles virus; Fusion protein; Membrane fusion; Refolding; Thermodynamic stability; Measles virus; Fusion protein; Membrane fusion; Refolding; Thermodynamic stability

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APA (6th Edition):

佐藤, . (2015). 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. (Thesis). Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学. Retrieved from http://id.nii.ac.jp/1211/00000017/

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):

佐藤, 友人. “麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.” 2015. Thesis, Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学. Accessed June 19, 2019. http://id.nii.ac.jp/1211/00000017/.

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

MLA Handbook (7th Edition):

佐藤, 友人. “麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.” 2015. Web. 19 Jun 2019.

Vancouver:

佐藤 . 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. [Internet] [Thesis]. Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学; 2015. [cited 2019 Jun 19]. Available from: http://id.nii.ac.jp/1211/00000017/.

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

Council of Science Editors:

佐藤 . 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. [Thesis]. Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学; 2015. Available from: http://id.nii.ac.jp/1211/00000017/

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

15. De, Mrinmoy. Engineering the Nanoparticle Surface for Protein Recognition and Applications.

Degree: PhD, Chemistry, 2009, U of Massachusetts : PhD

  Proteins and nanoparticles (NPs) provide a promising platform for supramolecular interaction. We are currently exploring both fundamental and applied aspects of this interaction. On… (more)

Subjects/Keywords: Nanoparticle; Protein refolding; Surface recognition; Thermodynamics; Protein recognition; Biochemistry; Chemistry

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

APA (6th Edition):

De, M. (2009). Engineering the Nanoparticle Surface for Protein Recognition and Applications. (Doctoral Dissertation). U of Massachusetts : PhD. Retrieved from https://scholarworks.umass.edu/open_access_dissertations/46

Chicago Manual of Style (16th Edition):

De, Mrinmoy. “Engineering the Nanoparticle Surface for Protein Recognition and Applications.” 2009. Doctoral Dissertation, U of Massachusetts : PhD. Accessed June 19, 2019. https://scholarworks.umass.edu/open_access_dissertations/46.

MLA Handbook (7th Edition):

De, Mrinmoy. “Engineering the Nanoparticle Surface for Protein Recognition and Applications.” 2009. Web. 19 Jun 2019.

Vancouver:

De M. Engineering the Nanoparticle Surface for Protein Recognition and Applications. [Internet] [Doctoral dissertation]. U of Massachusetts : PhD; 2009. [cited 2019 Jun 19]. Available from: https://scholarworks.umass.edu/open_access_dissertations/46.

Council of Science Editors:

De M. Engineering the Nanoparticle Surface for Protein Recognition and Applications. [Doctoral Dissertation]. U of Massachusetts : PhD; 2009. Available from: https://scholarworks.umass.edu/open_access_dissertations/46

16. Kaur, Harpreet. Investigation of Lysozyme Refolding Using Ionic Liquids as Refolding Additives.

Degree: 2013, University of Western Ontario

 A rapid and inexpensive method for the production of protein is crucial for the biopharmaceutical industry. The bottleneck in the case of genetically engineered systems… (more)

Subjects/Keywords: Protein refolding; Ionic liquids; On-column adsorptive refolding; Empirical Model; Biochemical and Biomolecular Engineering

…14 2.5 Role of refolding additives on protein refolding… …2.8 Role of ionic liquids as protein refolding additives… …30 2.8.1 Ionic liquid parameters that influence protein refolding… …32 2.9 Ionic liquids as protein refolding additives - Examples… …124 7 Adsorptive protein refolding with the aid of [EMIM] Cl in a packed bed… 

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APA (6th Edition):

Kaur, H. (2013). Investigation of Lysozyme Refolding Using Ionic Liquids as Refolding Additives. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1726

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):

Kaur, Harpreet. “Investigation of Lysozyme Refolding Using Ionic Liquids as Refolding Additives.” 2013. Thesis, University of Western Ontario. Accessed June 19, 2019. https://ir.lib.uwo.ca/etd/1726.

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

MLA Handbook (7th Edition):

Kaur, Harpreet. “Investigation of Lysozyme Refolding Using Ionic Liquids as Refolding Additives.” 2013. Web. 19 Jun 2019.

Vancouver:

Kaur H. Investigation of Lysozyme Refolding Using Ionic Liquids as Refolding Additives. [Internet] [Thesis]. University of Western Ontario; 2013. [cited 2019 Jun 19]. Available from: https://ir.lib.uwo.ca/etd/1726.

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

Council of Science Editors:

Kaur H. Investigation of Lysozyme Refolding Using Ionic Liquids as Refolding Additives. [Thesis]. University of Western Ontario; 2013. Available from: https://ir.lib.uwo.ca/etd/1726

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


The Ohio State University

17. Sen, Shiladitya. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.

Degree: PhD, Chemistry, 2013, The Ohio State University

 The inability to accurately decipher the relationship between a protein’s sequence and its structural stability presents a major difficulty in predicting the effects of mutation… (more)

Subjects/Keywords: Chemistry; Biochemistry; Protein engineering, High-throughput, Stability, Combinatorial library,Antibodies

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APA (6th Edition):

Sen, S. (2013). Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653

Chicago Manual of Style (16th Edition):

Sen, Shiladitya. “Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.” 2013. Doctoral Dissertation, The Ohio State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653.

MLA Handbook (7th Edition):

Sen, Shiladitya. “Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.” 2013. Web. 19 Jun 2019.

Vancouver:

Sen S. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653.

Council of Science Editors:

Sen S. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653

18. De Lima Damasceno, Bruno. Schistosoma Mansonii aspartic protease expression and refolding trials.

Degree: MA, Biochemistry & Molecular Biology, 2011, University of Kansas

 Schistosomiasis is a parasitic disease that causes considerable socio-economic losses in affected areas due to loss of productive capacity of affected individuals and high rates… (more)

Subjects/Keywords: Biochemistry; Biology; Chemistry; Protease; Protein disulfide isomerase; Refolding; Schistosoma

…more often leads to a lower fraction of active protein. Another major problem in refolding is… …evaluate the success of the refolding process. It is well known in modern protein folding… …refolding procedure could make the protein achieve a different folding and function than those… …refolding. 1D- Protein Disulfide Isomerases Protein disulfide isomerase (PDI) is a… …protein-cleaving enzyme 1), involved in accumulation of amyloid 9 forms in the brain… 

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APA (6th Edition):

De Lima Damasceno, B. (2011). Schistosoma Mansonii aspartic protease expression and refolding trials. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/9745

Chicago Manual of Style (16th Edition):

De Lima Damasceno, Bruno. “Schistosoma Mansonii aspartic protease expression and refolding trials.” 2011. Masters Thesis, University of Kansas. Accessed June 19, 2019. http://hdl.handle.net/1808/9745.

MLA Handbook (7th Edition):

De Lima Damasceno, Bruno. “Schistosoma Mansonii aspartic protease expression and refolding trials.” 2011. Web. 19 Jun 2019.

Vancouver:

De Lima Damasceno B. Schistosoma Mansonii aspartic protease expression and refolding trials. [Internet] [Masters thesis]. University of Kansas; 2011. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1808/9745.

Council of Science Editors:

De Lima Damasceno B. Schistosoma Mansonii aspartic protease expression and refolding trials. [Masters Thesis]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9745

19. NGUYEN THI KHANH THUYEN. Surface functionalization of nano-magnetic particle with beta cyclodextrin and its use in bio-molecule refolding process.

Degree: 2007, National University of Singapore

Subjects/Keywords: nano magnetic particles; beta cyclodextrin; lysozyme; refolding; denatured protein; aminopropyl

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APA (6th Edition):

THUYEN, N. T. K. (2007). Surface functionalization of nano-magnetic particle with beta cyclodextrin and its use in bio-molecule refolding process. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/16429

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):

THUYEN, NGUYEN THI KHANH. “Surface functionalization of nano-magnetic particle with beta cyclodextrin and its use in bio-molecule refolding process.” 2007. Thesis, National University of Singapore. Accessed June 19, 2019. http://scholarbank.nus.edu.sg/handle/10635/16429.

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

MLA Handbook (7th Edition):

THUYEN, NGUYEN THI KHANH. “Surface functionalization of nano-magnetic particle with beta cyclodextrin and its use in bio-molecule refolding process.” 2007. Web. 19 Jun 2019.

Vancouver:

THUYEN NTK. Surface functionalization of nano-magnetic particle with beta cyclodextrin and its use in bio-molecule refolding process. [Internet] [Thesis]. National University of Singapore; 2007. [cited 2019 Jun 19]. Available from: http://scholarbank.nus.edu.sg/handle/10635/16429.

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

Council of Science Editors:

THUYEN NTK. Surface functionalization of nano-magnetic particle with beta cyclodextrin and its use in bio-molecule refolding process. [Thesis]. National University of Singapore; 2007. Available from: http://scholarbank.nus.edu.sg/handle/10635/16429

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

20. D'Orchymont, Arnaud. Etudes structurales de l'ARN messager de l'histone H4 : Structural studies of histone H4 messenger RNA.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2013, Université de Strasbourg

Chez les Eucaryotes, l’étape d’initiation est de loin la plus complexe et la plus lente du processus de traduction. Elle nécessite l’intervention de 12 facteurs… (more)

Subjects/Keywords: MRNA; Refolding; Structure; Translation; Histone; MRNA; Refolding; Structure; Translation; Histone; 572.8

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APA (6th Edition):

D'Orchymont, A. (2013). Etudes structurales de l'ARN messager de l'histone H4 : Structural studies of histone H4 messenger RNA. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2013STRAJ039

Chicago Manual of Style (16th Edition):

D'Orchymont, Arnaud. “Etudes structurales de l'ARN messager de l'histone H4 : Structural studies of histone H4 messenger RNA.” 2013. Doctoral Dissertation, Université de Strasbourg. Accessed June 19, 2019. http://www.theses.fr/2013STRAJ039.

MLA Handbook (7th Edition):

D'Orchymont, Arnaud. “Etudes structurales de l'ARN messager de l'histone H4 : Structural studies of histone H4 messenger RNA.” 2013. Web. 19 Jun 2019.

Vancouver:

D'Orchymont A. Etudes structurales de l'ARN messager de l'histone H4 : Structural studies of histone H4 messenger RNA. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2013. [cited 2019 Jun 19]. Available from: http://www.theses.fr/2013STRAJ039.

Council of Science Editors:

D'Orchymont A. Etudes structurales de l'ARN messager de l'histone H4 : Structural studies of histone H4 messenger RNA. [Doctoral Dissertation]. Université de Strasbourg; 2013. Available from: http://www.theses.fr/2013STRAJ039


The Ohio State University

21. Ramasubramanian, Brinda. Combinatorial Approaches to Study Protein Stability: Design and Application of Cell-Based Screens to Engineer Tumor Suppressor Proteins.

Degree: PhD, Chemistry, 2011, The Ohio State University

  Tumor suppressor protein p53 is a transcription activation factor that is found mutated in more that 50 percent of human cancers. Despite its pathological… (more)

Subjects/Keywords: Biochemistry; Biophysics; Protein Engineering; p53 core domain; Tumor Supressor; combinatorial biophysics; cell-based screen

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APA (6th Edition):

Ramasubramanian, B. (2011). Combinatorial Approaches to Study Protein Stability: Design and Application of Cell-Based Screens to Engineer Tumor Suppressor Proteins. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1325256130

Chicago Manual of Style (16th Edition):

Ramasubramanian, Brinda. “Combinatorial Approaches to Study Protein Stability: Design and Application of Cell-Based Screens to Engineer Tumor Suppressor Proteins.” 2011. Doctoral Dissertation, The Ohio State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1325256130.

MLA Handbook (7th Edition):

Ramasubramanian, Brinda. “Combinatorial Approaches to Study Protein Stability: Design and Application of Cell-Based Screens to Engineer Tumor Suppressor Proteins.” 2011. Web. 19 Jun 2019.

Vancouver:

Ramasubramanian B. Combinatorial Approaches to Study Protein Stability: Design and Application of Cell-Based Screens to Engineer Tumor Suppressor Proteins. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1325256130.

Council of Science Editors:

Ramasubramanian B. Combinatorial Approaches to Study Protein Stability: Design and Application of Cell-Based Screens to Engineer Tumor Suppressor Proteins. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1325256130

22. Hallen, Mark Andrew. Protein and Drug Design Algorithms Using Improved Biophysical Modeling .

Degree: 2016, Duke University

  This thesis focuses on the development of algorithms that will allow protein design calculations to incorporate more realistic modeling assumptions. Protein design algorithms search… (more)

Subjects/Keywords: Computer science; Biochemistry; Algorithms; Bioinformatics; Combinatorial optimization; Computational biology; Drug design; Protein design

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APA (6th Edition):

Hallen, M. A. (2016). Protein and Drug Design Algorithms Using Improved Biophysical Modeling . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/12120

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):

Hallen, Mark Andrew. “Protein and Drug Design Algorithms Using Improved Biophysical Modeling .” 2016. Thesis, Duke University. Accessed June 19, 2019. http://hdl.handle.net/10161/12120.

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

MLA Handbook (7th Edition):

Hallen, Mark Andrew. “Protein and Drug Design Algorithms Using Improved Biophysical Modeling .” 2016. Web. 19 Jun 2019.

Vancouver:

Hallen MA. Protein and Drug Design Algorithms Using Improved Biophysical Modeling . [Internet] [Thesis]. Duke University; 2016. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10161/12120.

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

Council of Science Editors:

Hallen MA. Protein and Drug Design Algorithms Using Improved Biophysical Modeling . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/12120

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


University of Illinois – Chicago

23. Zhang, Ge. Spectroscopic Studies of Model Protein Interactions with Lipid Vesicles and Insulin Fibril Disassembly.

Degree: 2015, University of Illinois – Chicago

 The work in this thesis focuses on spectroscopic studies of refolding and interaction of model proteins with various lipid vesicles and on dimethyl sulfoxide (DMSO)-induced… (more)

Subjects/Keywords: β-lactoglobulin; phospholipid membrane vesicle; protein folding; fluorescence; CD; VCD; insulin fibril; DMSO-induced destabilization; amyloid; solvent effects; FTIR; ICD; TEM; refolding of outer membrane protein; SDS-PAGE; heat modifiability; dye leakage experiment

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APA (6th Edition):

Zhang, G. (2015). Spectroscopic Studies of Model Protein Interactions with Lipid Vesicles and Insulin Fibril Disassembly. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19818

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):

Zhang, Ge. “Spectroscopic Studies of Model Protein Interactions with Lipid Vesicles and Insulin Fibril Disassembly.” 2015. Thesis, University of Illinois – Chicago. Accessed June 19, 2019. http://hdl.handle.net/10027/19818.

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

MLA Handbook (7th Edition):

Zhang, Ge. “Spectroscopic Studies of Model Protein Interactions with Lipid Vesicles and Insulin Fibril Disassembly.” 2015. Web. 19 Jun 2019.

Vancouver:

Zhang G. Spectroscopic Studies of Model Protein Interactions with Lipid Vesicles and Insulin Fibril Disassembly. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10027/19818.

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

Council of Science Editors:

Zhang G. Spectroscopic Studies of Model Protein Interactions with Lipid Vesicles and Insulin Fibril Disassembly. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19818

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


Georgia Tech

24. Sinotte, Christopher Matthew. Construction, expression, and purification of soluble CD16 in bacteria.

Degree: MS, Bioengineering, 2006, Georgia Tech

 CD16 is a physiologically essential Fc and947; receptor III as either a single- pass transmembrane protein (CD16A) or as a glycosylated phosphatidylinositol (GPI) anchored protein(more)

Subjects/Keywords: X-ray crystallography; Protein refolding; Prokaryotic expression; CD16; X-ray crystallography; Protein folding; Prokaryotes; Microbial genetics

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APA (6th Edition):

Sinotte, C. M. (2006). Construction, expression, and purification of soluble CD16 in bacteria. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11510

Chicago Manual of Style (16th Edition):

Sinotte, Christopher Matthew. “Construction, expression, and purification of soluble CD16 in bacteria.” 2006. Masters Thesis, Georgia Tech. Accessed June 19, 2019. http://hdl.handle.net/1853/11510.

MLA Handbook (7th Edition):

Sinotte, Christopher Matthew. “Construction, expression, and purification of soluble CD16 in bacteria.” 2006. Web. 19 Jun 2019.

Vancouver:

Sinotte CM. Construction, expression, and purification of soluble CD16 in bacteria. [Internet] [Masters thesis]. Georgia Tech; 2006. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1853/11510.

Council of Science Editors:

Sinotte CM. Construction, expression, and purification of soluble CD16 in bacteria. [Masters Thesis]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/11510

25. Huang, Yuefei. A novel in vivo protein refolding technique.

Degree: PhD, Biochemistry and Molecular Biology, 2011, Wayne State University

  Proteins perform their functions in their native folded states and misfolding of proteins may cause severe diseases, including Alzheimer's disease, Parkinson's disease, prion disease… (more)

Subjects/Keywords: ER; folding machinery; in vivo; mammalian cells; protein delivery; protein refolding; Biochemistry

protein delivery ...88 2.3.4. Optimizing the in vivo protein refolding protocol for LBD… …western blot ....…131 3.3.4. Optimization of the protein refolding… …vivo protein refolding technique ..... …139 Table 3-2 Comparison of the… …6 The technical flow chat of the novel in vivo protein refolding technique developed by… …93 Figure 2-15 12% SDS-PAGEs, showing the in vivo protein refolding .…..95 Figure 2-16… 

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APA (6th Edition):

Huang, Y. (2011). A novel in vivo protein refolding technique. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/313

Chicago Manual of Style (16th Edition):

Huang, Yuefei. “A novel in vivo protein refolding technique.” 2011. Doctoral Dissertation, Wayne State University. Accessed June 19, 2019. https://digitalcommons.wayne.edu/oa_dissertations/313.

MLA Handbook (7th Edition):

Huang, Yuefei. “A novel in vivo protein refolding technique.” 2011. Web. 19 Jun 2019.

Vancouver:

Huang Y. A novel in vivo protein refolding technique. [Internet] [Doctoral dissertation]. Wayne State University; 2011. [cited 2019 Jun 19]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/313.

Council of Science Editors:

Huang Y. A novel in vivo protein refolding technique. [Doctoral Dissertation]. Wayne State University; 2011. Available from: https://digitalcommons.wayne.edu/oa_dissertations/313


Georgia Tech

26. Fellows, William Brett. Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties.

Degree: PhD, Chemistry and Biochemistry, 2014, Georgia Tech

 A new synthetic methodology for the combinatorial preparation of C-terminus-modified Green and Red Fluorescent Protein chromophores is described. This method involves the modification of the… (more)

Subjects/Keywords: Green fluorescent protein; Chromophore; Synthesis; Combinatorial; Red fluorescent protein; Hot dog stacking; Solid state; Crystal structure; Aggregate induced emission; Reprecipitation

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APA (6th Edition):

Fellows, W. B. (2014). Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52318

Chicago Manual of Style (16th Edition):

Fellows, William Brett. “Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties.” 2014. Doctoral Dissertation, Georgia Tech. Accessed June 19, 2019. http://hdl.handle.net/1853/52318.

MLA Handbook (7th Edition):

Fellows, William Brett. “Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties.” 2014. Web. 19 Jun 2019.

Vancouver:

Fellows WB. Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1853/52318.

Council of Science Editors:

Fellows WB. Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/52318

27. NG FUI MEE. Structural and functional studies of the NR2B subunit of NMDA receptor.

Degree: 2009, National University of Singapore

Subjects/Keywords: Circular dichroism; NMDA receptors; Amino-terminal domain of NR2B; Ifenprodil; Protein refolding; NR2B-NR2B disulfide-linked homo-dimer formation

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APA (6th Edition):

MEE, N. F. (2009). Structural and functional studies of the NR2B subunit of NMDA receptor. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/17627

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):

MEE, NG FUI. “Structural and functional studies of the NR2B subunit of NMDA receptor.” 2009. Thesis, National University of Singapore. Accessed June 19, 2019. http://scholarbank.nus.edu.sg/handle/10635/17627.

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

MLA Handbook (7th Edition):

MEE, NG FUI. “Structural and functional studies of the NR2B subunit of NMDA receptor.” 2009. Web. 19 Jun 2019.

Vancouver:

MEE NF. Structural and functional studies of the NR2B subunit of NMDA receptor. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2019 Jun 19]. Available from: http://scholarbank.nus.edu.sg/handle/10635/17627.

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

Council of Science Editors:

MEE NF. Structural and functional studies of the NR2B subunit of NMDA receptor. [Thesis]. National University of Singapore; 2009. Available from: http://scholarbank.nus.edu.sg/handle/10635/17627

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

28. ABU ZAYED MD BADRUDDOZA. Beta-cyclodextrin Conjugated Magnetic Nanoparticles for Bio-and Environmental Applications.

Degree: 2011, National University of Singapore

Subjects/Keywords: Magnetic nanoparticles; β-cyclodextrin; protein refolding; bioseparation; organic/inorganic pollutants removal; adsortion/desortption; drug inclusion

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APA (6th Edition):

BADRUDDOZA, A. Z. M. (2011). Beta-cyclodextrin Conjugated Magnetic Nanoparticles for Bio-and Environmental Applications. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/33321

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):

BADRUDDOZA, ABU ZAYED MD. “Beta-cyclodextrin Conjugated Magnetic Nanoparticles for Bio-and Environmental Applications.” 2011. Thesis, National University of Singapore. Accessed June 19, 2019. http://scholarbank.nus.edu.sg/handle/10635/33321.

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

MLA Handbook (7th Edition):

BADRUDDOZA, ABU ZAYED MD. “Beta-cyclodextrin Conjugated Magnetic Nanoparticles for Bio-and Environmental Applications.” 2011. Web. 19 Jun 2019.

Vancouver:

BADRUDDOZA AZM. Beta-cyclodextrin Conjugated Magnetic Nanoparticles for Bio-and Environmental Applications. [Internet] [Thesis]. National University of Singapore; 2011. [cited 2019 Jun 19]. Available from: http://scholarbank.nus.edu.sg/handle/10635/33321.

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

Council of Science Editors:

BADRUDDOZA AZM. Beta-cyclodextrin Conjugated Magnetic Nanoparticles for Bio-and Environmental Applications. [Thesis]. National University of Singapore; 2011. Available from: http://scholarbank.nus.edu.sg/handle/10635/33321

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


Georgia State University

29. Auguste, Rose. Optimizing the Production Parameters of Engineered Protein-Based MRI Contrast Agents.

Degree: MS, Chemistry, 2014, Georgia State University

  Magnetic Resonance Imaging is a noninvasive, complex imaging modality that uses contrast agents to enhance sensitivity and resolution for a clear image enhancement. To… (more)

Subjects/Keywords: Expression; Tag-less refolding method; GST-tag refolding; Gadolinium; Metal binding; Relaxivity; Structural Conformation

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APA (6th Edition):

Auguste, R. (2014). Optimizing the Production Parameters of Engineered Protein-Based MRI Contrast Agents. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/61

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):

Auguste, Rose. “Optimizing the Production Parameters of Engineered Protein-Based MRI Contrast Agents.” 2014. Thesis, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_theses/61.

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

MLA Handbook (7th Edition):

Auguste, Rose. “Optimizing the Production Parameters of Engineered Protein-Based MRI Contrast Agents.” 2014. Web. 19 Jun 2019.

Vancouver:

Auguste R. Optimizing the Production Parameters of Engineered Protein-Based MRI Contrast Agents. [Internet] [Thesis]. Georgia State University; 2014. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_theses/61.

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

Council of Science Editors:

Auguste R. Optimizing the Production Parameters of Engineered Protein-Based MRI Contrast Agents. [Thesis]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/chemistry_theses/61

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


The Ohio State University

30. Li, Weiyi. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.

Degree: MS, Chemistry, 2014, The Ohio State University

 The sequence-structure-stability relationship is a key problem in the field of protein science. Although a large amount of research has been working on it in… (more)

Subjects/Keywords: Biochemistry; Chemistry; Biophysics; Biology; Rop, Rosetta, protein G, combinatorial library, hydrophobic core library, computational design, high-throughput

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

APA (6th Edition):

Li, W. (2014). Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266

Chicago Manual of Style (16th Edition):

Li, Weiyi. “Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.” 2014. Masters Thesis, The Ohio State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266.

MLA Handbook (7th Edition):

Li, Weiyi. “Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.” 2014. Web. 19 Jun 2019.

Vancouver:

Li W. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. [Internet] [Masters thesis]. The Ohio State University; 2014. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266.

Council of Science Editors:

Li W. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. [Masters Thesis]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266

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