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You searched for subject:(maltose binding protein affinity chromatography). Showing records 1 – 30 of 26675 total matches.

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Miami University

1. New, Christopher Paul. Analysis of Tha4 Function and Organization in Chloroplast Twin Arginine Transport.

Degree: PhD, Cell, Molecular and Structural Biology (CMSB), 2020, Miami University

 The chloroplast Twin Arginine Translocase (cpTAT) system transports fully folded proteins across the thylakoid membrane in plant cells using only energy derived from the proton… (more)

Subjects/Keywords: Biochemistry; Cellular Biology; Plant Biology; Molecular Biology; chloroplast twin arginine transport; protein transport; cpTAT; TAT; Tha4; Hcf106; protein purification; maltose binding protein affinity chromatography; oligomer formation; complementation; transmembrane domain hydrophobicity

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

APA (6th Edition):

New, C. P. (2020). Analysis of Tha4 Function and Organization in Chloroplast Twin Arginine Transport. (Doctoral Dissertation). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1586878527570538

Chicago Manual of Style (16th Edition):

New, Christopher Paul. “Analysis of Tha4 Function and Organization in Chloroplast Twin Arginine Transport.” 2020. Doctoral Dissertation, Miami University. Accessed January 18, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=miami1586878527570538.

MLA Handbook (7th Edition):

New, Christopher Paul. “Analysis of Tha4 Function and Organization in Chloroplast Twin Arginine Transport.” 2020. Web. 18 Jan 2021.

Vancouver:

New CP. Analysis of Tha4 Function and Organization in Chloroplast Twin Arginine Transport. [Internet] [Doctoral dissertation]. Miami University; 2020. [cited 2021 Jan 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1586878527570538.

Council of Science Editors:

New CP. Analysis of Tha4 Function and Organization in Chloroplast Twin Arginine Transport. [Doctoral Dissertation]. Miami University; 2020. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1586878527570538

2. Merstorf, Céline. Stabilité conformationnelle et dépliement de la protéine MalE : Étude par nanopore et par spectroscopie RMN : Conformationnal stability and unfolding of the maltose binding protein.

Degree: Docteur es, Physique, 2011, Cergy-Pontoise

Nous avons étudié le couplage dépliement-transport de la Maltose Binding Protein (MBP ou MalE), une protéine périplasmique d'E. Coli et d'un mutant instable, le MalE219,… (more)

Subjects/Keywords: Repliement; Dépliement; Proteine; Technique nanopore; Maltose binding Protein; Folding; Unfolding; Protein; Nanopore recording technique; Maltose Binding Protein

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APA (6th Edition):

Merstorf, C. (2011). Stabilité conformationnelle et dépliement de la protéine MalE : Étude par nanopore et par spectroscopie RMN : Conformationnal stability and unfolding of the maltose binding protein. (Doctoral Dissertation). Cergy-Pontoise. Retrieved from http://www.theses.fr/2011CERG0571

Chicago Manual of Style (16th Edition):

Merstorf, Céline. “Stabilité conformationnelle et dépliement de la protéine MalE : Étude par nanopore et par spectroscopie RMN : Conformationnal stability and unfolding of the maltose binding protein.” 2011. Doctoral Dissertation, Cergy-Pontoise. Accessed January 18, 2021. http://www.theses.fr/2011CERG0571.

MLA Handbook (7th Edition):

Merstorf, Céline. “Stabilité conformationnelle et dépliement de la protéine MalE : Étude par nanopore et par spectroscopie RMN : Conformationnal stability and unfolding of the maltose binding protein.” 2011. Web. 18 Jan 2021.

Vancouver:

Merstorf C. Stabilité conformationnelle et dépliement de la protéine MalE : Étude par nanopore et par spectroscopie RMN : Conformationnal stability and unfolding of the maltose binding protein. [Internet] [Doctoral dissertation]. Cergy-Pontoise; 2011. [cited 2021 Jan 18]. Available from: http://www.theses.fr/2011CERG0571.

Council of Science Editors:

Merstorf C. Stabilité conformationnelle et dépliement de la protéine MalE : Étude par nanopore et par spectroscopie RMN : Conformationnal stability and unfolding of the maltose binding protein. [Doctoral Dissertation]. Cergy-Pontoise; 2011. Available from: http://www.theses.fr/2011CERG0571


University of Bradford

3. Saleem, Saira. Proteomic profiling of pro and active matrix metalloproteinases using tandem mass spectrometry. optimization of affinity chromatography and nHPLC-MALDI-MS/MS for proteomic discrimination of matrix metalloproteinases in pre-clinical cancer model.

Degree: PhD, 2012, University of Bradford

 Matrix metalloproteinases (MMPs) network with other biological molecules to maintain the extracellular matrix (ECM) in normal physiology and perform different roles. Understanding and assigning specific… (more)

Subjects/Keywords: 616.99; Matrix metalloproteinases (MMPs); Proteomic profiling; Tandem Mass Spectrometry; Affinity Chromatography; nHPLC-MALDI-MS/MS; Pre-clinical Cancer; Protein binding

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APA (6th Edition):

Saleem, S. (2012). Proteomic profiling of pro and active matrix metalloproteinases using tandem mass spectrometry. optimization of affinity chromatography and nHPLC-MALDI-MS/MS for proteomic discrimination of matrix metalloproteinases in pre-clinical cancer model. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/5752

Chicago Manual of Style (16th Edition):

Saleem, Saira. “Proteomic profiling of pro and active matrix metalloproteinases using tandem mass spectrometry. optimization of affinity chromatography and nHPLC-MALDI-MS/MS for proteomic discrimination of matrix metalloproteinases in pre-clinical cancer model.” 2012. Doctoral Dissertation, University of Bradford. Accessed January 18, 2021. http://hdl.handle.net/10454/5752.

MLA Handbook (7th Edition):

Saleem, Saira. “Proteomic profiling of pro and active matrix metalloproteinases using tandem mass spectrometry. optimization of affinity chromatography and nHPLC-MALDI-MS/MS for proteomic discrimination of matrix metalloproteinases in pre-clinical cancer model.” 2012. Web. 18 Jan 2021.

Vancouver:

Saleem S. Proteomic profiling of pro and active matrix metalloproteinases using tandem mass spectrometry. optimization of affinity chromatography and nHPLC-MALDI-MS/MS for proteomic discrimination of matrix metalloproteinases in pre-clinical cancer model. [Internet] [Doctoral dissertation]. University of Bradford; 2012. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10454/5752.

Council of Science Editors:

Saleem S. Proteomic profiling of pro and active matrix metalloproteinases using tandem mass spectrometry. optimization of affinity chromatography and nHPLC-MALDI-MS/MS for proteomic discrimination of matrix metalloproteinases in pre-clinical cancer model. [Doctoral Dissertation]. University of Bradford; 2012. Available from: http://hdl.handle.net/10454/5752


Texas Tech University

4. Sherrod, Peter D. Applications of affinity chromatography to isolation of sequence specific nuclear proteins.

Degree: Chemistry, 1981, Texas Tech University

 Even before Watson and Crick proposed their brilliant model for the structure of DNA, Jacob and Monod were busy piecing together the information that would… (more)

Subjects/Keywords: Genetic regulation; Affinity chromatography; Deoxyribonucleic acid (DNA); Protein binding

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APA (6th Edition):

Sherrod, P. D. (1981). Applications of affinity chromatography to isolation of sequence specific nuclear proteins. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/18940

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):

Sherrod, Peter D. “Applications of affinity chromatography to isolation of sequence specific nuclear proteins.” 1981. Thesis, Texas Tech University. Accessed January 18, 2021. http://hdl.handle.net/2346/18940.

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

MLA Handbook (7th Edition):

Sherrod, Peter D. “Applications of affinity chromatography to isolation of sequence specific nuclear proteins.” 1981. Web. 18 Jan 2021.

Vancouver:

Sherrod PD. Applications of affinity chromatography to isolation of sequence specific nuclear proteins. [Internet] [Thesis]. Texas Tech University; 1981. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/2346/18940.

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

Council of Science Editors:

Sherrod PD. Applications of affinity chromatography to isolation of sequence specific nuclear proteins. [Thesis]. Texas Tech University; 1981. Available from: http://hdl.handle.net/2346/18940

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


Indian Institute of Science

5. Sharma, Likhesh. Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 Chapter 1gives a general introduction to the CXXC motif found in natural proteins. It then reviews the studies where disulphides were engineered in various proteins.… (more)

Subjects/Keywords: Engineering Disulphide Bonds; Signal Peptides; Maltose Binding Protein; Protein Stability; Protein Export; E.coli Thioredoxin; Maltose-binding Protein (MBP); Cysteine Mutation; Molecular Biophysics

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APA (6th Edition):

Sharma, L. (2018). Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3746

Chicago Manual of Style (16th Edition):

Sharma, Likhesh. “Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed January 18, 2021. http://etd.iisc.ac.in/handle/2005/3746.

MLA Handbook (7th Edition):

Sharma, Likhesh. “Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides.” 2018. Web. 18 Jan 2021.

Vancouver:

Sharma L. Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Jan 18]. Available from: http://etd.iisc.ac.in/handle/2005/3746.

Council of Science Editors:

Sharma L. Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3746


Purdue University

6. Huang, Yan. Interaction Between Maltose Binding Protein And Escherichia Coli Maltose Transporter.

Degree: MS, Biological Science, 2013, Purdue University

  The ATP-binding cassette (ABC) transporter superfamily is one of the largest families of transport proteins. The ABC transporters are responsible for selective permeability of… (more)

Subjects/Keywords: ABC Transporter; EPR; Escheria-Coli; Maltose-Binding Protein; Mechnism; Membrane-Protein; Biochemistry; Biology; Biophysics

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APA (6th Edition):

Huang, Y. (2013). Interaction Between Maltose Binding Protein And Escherichia Coli Maltose Transporter. (Thesis). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_theses/43

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):

Huang, Yan. “Interaction Between Maltose Binding Protein And Escherichia Coli Maltose Transporter.” 2013. Thesis, Purdue University. Accessed January 18, 2021. http://docs.lib.purdue.edu/open_access_theses/43.

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

MLA Handbook (7th Edition):

Huang, Yan. “Interaction Between Maltose Binding Protein And Escherichia Coli Maltose Transporter.” 2013. Web. 18 Jan 2021.

Vancouver:

Huang Y. Interaction Between Maltose Binding Protein And Escherichia Coli Maltose Transporter. [Internet] [Thesis]. Purdue University; 2013. [cited 2021 Jan 18]. Available from: http://docs.lib.purdue.edu/open_access_theses/43.

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

Council of Science Editors:

Huang Y. Interaction Between Maltose Binding Protein And Escherichia Coli Maltose Transporter. [Thesis]. Purdue University; 2013. Available from: http://docs.lib.purdue.edu/open_access_theses/43

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


University of Western Ontario

7. Gould, Alister D. ATPase Regulation in the Maltose Transporter.

Degree: 2011, University of Western Ontario

 This thesis investigates the mechanism of activity-coupling in the maltose transporter of Escherichia coli (MalFGK2); the way ATP hydrolysis is prevented in the absence of… (more)

Subjects/Keywords: Active Transport; ATP Binding Cassette; ATPase; Escherichia Coli; Cell Membrane; Maltose Binding Protein; Maltose Transport; Protein Conformation; Substrate Specificity; X-ray Crystallography; Biochemistry; Structural Biology

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APA (6th Edition):

Gould, A. D. (2011). ATPase Regulation in the Maltose Transporter. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/374

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):

Gould, Alister D. “ATPase Regulation in the Maltose Transporter.” 2011. Thesis, University of Western Ontario. Accessed January 18, 2021. https://ir.lib.uwo.ca/etd/374.

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

MLA Handbook (7th Edition):

Gould, Alister D. “ATPase Regulation in the Maltose Transporter.” 2011. Web. 18 Jan 2021.

Vancouver:

Gould AD. ATPase Regulation in the Maltose Transporter. [Internet] [Thesis]. University of Western Ontario; 2011. [cited 2021 Jan 18]. Available from: https://ir.lib.uwo.ca/etd/374.

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

Council of Science Editors:

Gould AD. ATPase Regulation in the Maltose Transporter. [Thesis]. University of Western Ontario; 2011. Available from: https://ir.lib.uwo.ca/etd/374

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


Rochester Institute of Technology

8. Judd, Deborah. The Search for the active site configuration of glutamate dehydrogenase i) Reactivity of LYS-126 ii) Preparation of O-Se-NADP+.

Degree: School of Chemistry and Materials Science (COS), 1991, Rochester Institute of Technology

None provided. Advisors/Committee Members: Bell, J..

Subjects/Keywords: Binding sites; Affinity chromatography; Reactivity

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APA (6th Edition):

Judd, D. (1991). The Search for the active site configuration of glutamate dehydrogenase i) Reactivity of LYS-126 ii) Preparation of O-Se-NADP+. (Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/4897

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):

Judd, Deborah. “The Search for the active site configuration of glutamate dehydrogenase i) Reactivity of LYS-126 ii) Preparation of O-Se-NADP+.” 1991. Thesis, Rochester Institute of Technology. Accessed January 18, 2021. https://scholarworks.rit.edu/theses/4897.

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

MLA Handbook (7th Edition):

Judd, Deborah. “The Search for the active site configuration of glutamate dehydrogenase i) Reactivity of LYS-126 ii) Preparation of O-Se-NADP+.” 1991. Web. 18 Jan 2021.

Vancouver:

Judd D. The Search for the active site configuration of glutamate dehydrogenase i) Reactivity of LYS-126 ii) Preparation of O-Se-NADP+. [Internet] [Thesis]. Rochester Institute of Technology; 1991. [cited 2021 Jan 18]. Available from: https://scholarworks.rit.edu/theses/4897.

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

Council of Science Editors:

Judd D. The Search for the active site configuration of glutamate dehydrogenase i) Reactivity of LYS-126 ii) Preparation of O-Se-NADP+. [Thesis]. Rochester Institute of Technology; 1991. Available from: https://scholarworks.rit.edu/theses/4897

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


University of Georgia

9. Samli, Kausar Nadim. Lectenz.

Degree: 2017, University of Georgia

 Carbohydrate recognition is an integral part of normal biological processes. It is critical for host-pathogen interactions, biological development, and increasingly important for disease-state biomarker detection.… (more)

Subjects/Keywords: Lectenz; Lectin; Glycan; Protein engineering; Directed evolution; Molecular dynamics; MM-GBSA; Binding free energy decomposition; Glycosylation; PNGase F; Yeast display; Glycosensors; Biosensors; Affinity chromatography; Glycoprofiling

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APA (6th Edition):

Samli, K. N. (2017). Lectenz. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/36825

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):

Samli, Kausar Nadim. “Lectenz.” 2017. Thesis, University of Georgia. Accessed January 18, 2021. http://hdl.handle.net/10724/36825.

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

MLA Handbook (7th Edition):

Samli, Kausar Nadim. “Lectenz.” 2017. Web. 18 Jan 2021.

Vancouver:

Samli KN. Lectenz. [Internet] [Thesis]. University of Georgia; 2017. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10724/36825.

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

Council of Science Editors:

Samli KN. Lectenz. [Thesis]. University of Georgia; 2017. Available from: http://hdl.handle.net/10724/36825

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


Brandeis University

10. Karmakar, Chinmoyee. A strategy to label RNA for visualization.

Degree: 2014, Brandeis University

 Many experimental studies require the isolation of multi-subunit RNA-protein complexes for detailed analysis and characterization. It would be highly advantageous if an investigator could site-specifically… (more)

Subjects/Keywords: Truncated Proteins; Splicesosomal Protein U1A; RNA binding Protein; U1A RNP; Riboncleoprotein, Protein Purification; His tagged Proteins; NiNTA affinity Chromatography; Invitrotranscription; SP sepharose Ion exchange Chromatography; Nickel-tris-nitrilotriacetic acid reagent; Ni-TrisNTA; QuikChange PCR; pET plasmid

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APA (6th Edition):

Karmakar, C. (2014). A strategy to label RNA for visualization. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/26291

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):

Karmakar, Chinmoyee. “A strategy to label RNA for visualization.” 2014. Thesis, Brandeis University. Accessed January 18, 2021. http://hdl.handle.net/10192/26291.

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

MLA Handbook (7th Edition):

Karmakar, Chinmoyee. “A strategy to label RNA for visualization.” 2014. Web. 18 Jan 2021.

Vancouver:

Karmakar C. A strategy to label RNA for visualization. [Internet] [Thesis]. Brandeis University; 2014. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10192/26291.

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

Council of Science Editors:

Karmakar C. A strategy to label RNA for visualization. [Thesis]. Brandeis University; 2014. Available from: http://hdl.handle.net/10192/26291

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


University of Pennsylvania

11. Walters, Benjamin Thomas. Large Protein Folding and Dynamics Studied by Advanced Hydrogen Exchange Methods.

Degree: 2013, University of Pennsylvania

Protein folding studies over the past 50 years have been largely focused on small proteins (< 200 residues) leading to a dearth of information about… (more)

Subjects/Keywords: Collapse; Denatured State Ensemble DSE; HDX MS; Hydrogen Exchange; Maltose Binding Protein; Protein Folding; Analytical Chemistry; Biochemistry; Biophysics

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APA (6th Edition):

Walters, B. T. (2013). Large Protein Folding and Dynamics Studied by Advanced Hydrogen Exchange Methods. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/937

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):

Walters, Benjamin Thomas. “Large Protein Folding and Dynamics Studied by Advanced Hydrogen Exchange Methods.” 2013. Thesis, University of Pennsylvania. Accessed January 18, 2021. https://repository.upenn.edu/edissertations/937.

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

MLA Handbook (7th Edition):

Walters, Benjamin Thomas. “Large Protein Folding and Dynamics Studied by Advanced Hydrogen Exchange Methods.” 2013. Web. 18 Jan 2021.

Vancouver:

Walters BT. Large Protein Folding and Dynamics Studied by Advanced Hydrogen Exchange Methods. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2021 Jan 18]. Available from: https://repository.upenn.edu/edissertations/937.

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

Council of Science Editors:

Walters BT. Large Protein Folding and Dynamics Studied by Advanced Hydrogen Exchange Methods. [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/937

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


Queens University

12. Delorme, Caroline. Structural and Functional Characterization of a Novel Heterodimeric Kinesin in Candida albicans .

Degree: Biochemistry, 2012, Queens University

 Kinesins are molecular motors that transport intracellular cargos along microtubules (MTs) and influence the organization and dynamics of the MT cytoskeleton. Their force-generating functions arise… (more)

Subjects/Keywords: Filamentous Fungus ; Kinesin-14 ; Kar3 ; Candida Albicans ; Switch Elements ; Maltose Binding Protein ; Microtubule Motor Protein ; ATPase activity

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APA (6th Edition):

Delorme, C. (2012). Structural and Functional Characterization of a Novel Heterodimeric Kinesin in Candida albicans . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/7023

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):

Delorme, Caroline. “Structural and Functional Characterization of a Novel Heterodimeric Kinesin in Candida albicans .” 2012. Thesis, Queens University. Accessed January 18, 2021. http://hdl.handle.net/1974/7023.

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

MLA Handbook (7th Edition):

Delorme, Caroline. “Structural and Functional Characterization of a Novel Heterodimeric Kinesin in Candida albicans .” 2012. Web. 18 Jan 2021.

Vancouver:

Delorme C. Structural and Functional Characterization of a Novel Heterodimeric Kinesin in Candida albicans . [Internet] [Thesis]. Queens University; 2012. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1974/7023.

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

Council of Science Editors:

Delorme C. Structural and Functional Characterization of a Novel Heterodimeric Kinesin in Candida albicans . [Thesis]. Queens University; 2012. Available from: http://hdl.handle.net/1974/7023

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


Virginia Tech

13. Sines, Brian James. Evaluation of Phenomena that Determine the Performance of Immunoaffinity, Peptide-Based and Ion Exchange Affinity Sorbents.

Degree: PhD, Chemical Engineering, 2000, Virginia Tech

 This report presents an evaluation of the design of low-solids content, large-particle diameter beaded cellulose supports for column-mode protein purification. The study presented here optimizes… (more)

Subjects/Keywords: affinity chromatography; protein purification

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APA (6th Edition):

Sines, B. J. (2000). Evaluation of Phenomena that Determine the Performance of Immunoaffinity, Peptide-Based and Ion Exchange Affinity Sorbents. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/29841

Chicago Manual of Style (16th Edition):

Sines, Brian James. “Evaluation of Phenomena that Determine the Performance of Immunoaffinity, Peptide-Based and Ion Exchange Affinity Sorbents.” 2000. Doctoral Dissertation, Virginia Tech. Accessed January 18, 2021. http://hdl.handle.net/10919/29841.

MLA Handbook (7th Edition):

Sines, Brian James. “Evaluation of Phenomena that Determine the Performance of Immunoaffinity, Peptide-Based and Ion Exchange Affinity Sorbents.” 2000. Web. 18 Jan 2021.

Vancouver:

Sines BJ. Evaluation of Phenomena that Determine the Performance of Immunoaffinity, Peptide-Based and Ion Exchange Affinity Sorbents. [Internet] [Doctoral dissertation]. Virginia Tech; 2000. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10919/29841.

Council of Science Editors:

Sines BJ. Evaluation of Phenomena that Determine the Performance of Immunoaffinity, Peptide-Based and Ion Exchange Affinity Sorbents. [Doctoral Dissertation]. Virginia Tech; 2000. Available from: http://hdl.handle.net/10919/29841


University of Minnesota

14. Cai, Yijian. Effects of Active Site Inhibitors on APN-dependent Coronavirus Entry.

Degree: MS, Pharmacology, 2017, University of Minnesota

 Aminopeptidase N(APN) has been shown as a receptor of several coronaviruses, such as HCoV-229E, TGEV, CCoV and FeCoV. Bestatin and Actinonin are inhibitors which can… (more)

Subjects/Keywords: Aminopeptidase N; binding affinity; Coronavirus; inhibitor; protein expression; pseudovirus entry

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APA (6th Edition):

Cai, Y. (2017). Effects of Active Site Inhibitors on APN-dependent Coronavirus Entry. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/206195

Chicago Manual of Style (16th Edition):

Cai, Yijian. “Effects of Active Site Inhibitors on APN-dependent Coronavirus Entry.” 2017. Masters Thesis, University of Minnesota. Accessed January 18, 2021. http://hdl.handle.net/11299/206195.

MLA Handbook (7th Edition):

Cai, Yijian. “Effects of Active Site Inhibitors on APN-dependent Coronavirus Entry.” 2017. Web. 18 Jan 2021.

Vancouver:

Cai Y. Effects of Active Site Inhibitors on APN-dependent Coronavirus Entry. [Internet] [Masters thesis]. University of Minnesota; 2017. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11299/206195.

Council of Science Editors:

Cai Y. Effects of Active Site Inhibitors on APN-dependent Coronavirus Entry. [Masters Thesis]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/206195


University of Georgia

15. Ji, Ye. Using biolayer interferometry to quantify monomeric solution affinities for carbohydrate-protein interactions.

Degree: 2018, University of Georgia

 Many biological events involve carbohydrates binding to protein receptors (lectins, antibodies, enzymes, etc). The carbohydrates are often present as glycoproteins or glycopids that may be… (more)

Subjects/Keywords: Carbohydrate-protein interaction; binding affinity; KD; monomeric; multimeric

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APA (6th Edition):

Ji, Y. (2018). Using biolayer interferometry to quantify monomeric solution affinities for carbohydrate-protein interactions. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/38340

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):

Ji, Ye. “Using biolayer interferometry to quantify monomeric solution affinities for carbohydrate-protein interactions.” 2018. Thesis, University of Georgia. Accessed January 18, 2021. http://hdl.handle.net/10724/38340.

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

MLA Handbook (7th Edition):

Ji, Ye. “Using biolayer interferometry to quantify monomeric solution affinities for carbohydrate-protein interactions.” 2018. Web. 18 Jan 2021.

Vancouver:

Ji Y. Using biolayer interferometry to quantify monomeric solution affinities for carbohydrate-protein interactions. [Internet] [Thesis]. University of Georgia; 2018. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10724/38340.

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

Council of Science Editors:

Ji Y. Using biolayer interferometry to quantify monomeric solution affinities for carbohydrate-protein interactions. [Thesis]. University of Georgia; 2018. Available from: http://hdl.handle.net/10724/38340

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


Indian Institute of Science

16. Ganesh, C. Thermodynamic & Kinetic Characterization Of The Folding Of E.coli Maltose-Binding Protein.

Degree: PhD, Faculty of Science, 2011, Indian Institute of Science

Subjects/Keywords: Proteins - Thermodynamics; Proteins - Molecular Biology; Maltose Binding Protein; Biochemistry

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APA (6th Edition):

Ganesh, C. (2011). Thermodynamic & Kinetic Characterization Of The Folding Of E.coli Maltose-Binding Protein. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/1537

Chicago Manual of Style (16th Edition):

Ganesh, C. “Thermodynamic & Kinetic Characterization Of The Folding Of E.coli Maltose-Binding Protein.” 2011. Doctoral Dissertation, Indian Institute of Science. Accessed January 18, 2021. http://etd.iisc.ac.in/handle/2005/1537.

MLA Handbook (7th Edition):

Ganesh, C. “Thermodynamic & Kinetic Characterization Of The Folding Of E.coli Maltose-Binding Protein.” 2011. Web. 18 Jan 2021.

Vancouver:

Ganesh C. Thermodynamic & Kinetic Characterization Of The Folding Of E.coli Maltose-Binding Protein. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2011. [cited 2021 Jan 18]. Available from: http://etd.iisc.ac.in/handle/2005/1537.

Council of Science Editors:

Ganesh C. Thermodynamic & Kinetic Characterization Of The Folding Of E.coli Maltose-Binding Protein. [Doctoral Dissertation]. Indian Institute of Science; 2011. Available from: http://etd.iisc.ac.in/handle/2005/1537


University of Illinois – Urbana-Champaign

17. Wen, Po-Chao. Mechanistic studies of ABC transporters.

Degree: PhD, 0319, 2013, University of Illinois – Urbana-Champaign

 ATP-binding cassette (ABC) transporters are a superfamily of primary membrane transporters that are abundant yet highly diverse in structures and functions. These proteins power the… (more)

Subjects/Keywords: ATP-binding cassette (ABC) transporters transporters; Molecular dynamics; Membrane transport; Protein dynamics; Conformational change; Maltose transporter; P-Glycoprotein

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APA (6th Edition):

Wen, P. (2013). Mechanistic studies of ABC transporters. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45599

Chicago Manual of Style (16th Edition):

Wen, Po-Chao. “Mechanistic studies of ABC transporters.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 18, 2021. http://hdl.handle.net/2142/45599.

MLA Handbook (7th Edition):

Wen, Po-Chao. “Mechanistic studies of ABC transporters.” 2013. Web. 18 Jan 2021.

Vancouver:

Wen P. Mechanistic studies of ABC transporters. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/2142/45599.

Council of Science Editors:

Wen P. Mechanistic studies of ABC transporters. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45599


University of Toronto

18. Ryan, Timothy. Identification of Ryanodine Receptor 1 (RyR1) Interacting Protein Partners Using Liquid Chromatography and Mass Spectrometry.

Degree: 2010, University of Toronto

Ryanodine receptor 1 (RyR1) is a homotetrameric calcium channel located in the sarcoplasmic reticulum (SR) of skeletal muscle. We employed metal affinity chromatography followed by… (more)

Subjects/Keywords: Ryanodine Receptor 1; Metal affinity chromatography; Mass Spectrometry; Protein-protein interactions; 0719

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

APA (6th Edition):

Ryan, T. (2010). Identification of Ryanodine Receptor 1 (RyR1) Interacting Protein Partners Using Liquid Chromatography and Mass Spectrometry. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25911

Chicago Manual of Style (16th Edition):

Ryan, Timothy. “Identification of Ryanodine Receptor 1 (RyR1) Interacting Protein Partners Using Liquid Chromatography and Mass Spectrometry.” 2010. Masters Thesis, University of Toronto. Accessed January 18, 2021. http://hdl.handle.net/1807/25911.

MLA Handbook (7th Edition):

Ryan, Timothy. “Identification of Ryanodine Receptor 1 (RyR1) Interacting Protein Partners Using Liquid Chromatography and Mass Spectrometry.” 2010. Web. 18 Jan 2021.

Vancouver:

Ryan T. Identification of Ryanodine Receptor 1 (RyR1) Interacting Protein Partners Using Liquid Chromatography and Mass Spectrometry. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1807/25911.

Council of Science Editors:

Ryan T. Identification of Ryanodine Receptor 1 (RyR1) Interacting Protein Partners Using Liquid Chromatography and Mass Spectrometry. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25911


Vanderbilt University

19. Allison, Brittany Ann. Computational Design of Protein-Ligand Interfaces Using RosettaLigand.

Degree: PhD, Chemistry, 2016, Vanderbilt University

 Computational design of protein-ligand interfaces expands understanding of the basic forces involved in molecular recognition, and also contributes to the development of protein therapeutics. My… (more)

Subjects/Keywords: protein engineering; protein ligand binding; RosettaLigand; Rosetta; protein small molecule interactions; interface design; computational design; ligand macromolecule recognition; NMR; binding affinity

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APA (6th Edition):

Allison, B. A. (2016). Computational Design of Protein-Ligand Interfaces Using RosettaLigand. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11616

Chicago Manual of Style (16th Edition):

Allison, Brittany Ann. “Computational Design of Protein-Ligand Interfaces Using RosettaLigand.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 18, 2021. http://hdl.handle.net/1803/11616.

MLA Handbook (7th Edition):

Allison, Brittany Ann. “Computational Design of Protein-Ligand Interfaces Using RosettaLigand.” 2016. Web. 18 Jan 2021.

Vancouver:

Allison BA. Computational Design of Protein-Ligand Interfaces Using RosettaLigand. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1803/11616.

Council of Science Editors:

Allison BA. Computational Design of Protein-Ligand Interfaces Using RosettaLigand. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/11616


Ryerson University

20. Dufresne, Jaimie. The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry.

Degree: 2017, Ryerson University

 Cell surface receptors are of critical importance to the treatment of disease but are difficult to isolate and identify by classical approaches. Here, a robust… (more)

Subjects/Keywords: Cell receptors; Cell membranes; Ligands; Fc receptors; Ligand binding (Biochemistry); Receptor-ligand complexes; Affinity chromatography; Liquid chromatography; Tandem mass spectometry

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APA (6th Edition):

Dufresne, J. (2017). The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A7225

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):

Dufresne, Jaimie. “The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry.” 2017. Thesis, Ryerson University. Accessed January 18, 2021. https://digital.library.ryerson.ca/islandora/object/RULA%3A7225.

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

MLA Handbook (7th Edition):

Dufresne, Jaimie. “The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry.” 2017. Web. 18 Jan 2021.

Vancouver:

Dufresne J. The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry. [Internet] [Thesis]. Ryerson University; 2017. [cited 2021 Jan 18]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A7225.

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

Council of Science Editors:

Dufresne J. The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry. [Thesis]. Ryerson University; 2017. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A7225

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


Clemson University

21. Trang, Hung Khiem. Development of Functionalized Capillary-Channeled Polymer (C-CP) Fibers as Stationary Phase for Affinity Chromatography.

Degree: PhD, Chemistry, 2019, Clemson University

  At the heart of the chromatography technique, the stationary phase is the essential component that dictates multiple aspects of the separation process. Diverse chemistry… (more)

Subjects/Keywords: affinity; chromatography; fiber

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APA (6th Edition):

Trang, H. K. (2019). Development of Functionalized Capillary-Channeled Polymer (C-CP) Fibers as Stationary Phase for Affinity Chromatography. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/2532

Chicago Manual of Style (16th Edition):

Trang, Hung Khiem. “Development of Functionalized Capillary-Channeled Polymer (C-CP) Fibers as Stationary Phase for Affinity Chromatography.” 2019. Doctoral Dissertation, Clemson University. Accessed January 18, 2021. https://tigerprints.clemson.edu/all_dissertations/2532.

MLA Handbook (7th Edition):

Trang, Hung Khiem. “Development of Functionalized Capillary-Channeled Polymer (C-CP) Fibers as Stationary Phase for Affinity Chromatography.” 2019. Web. 18 Jan 2021.

Vancouver:

Trang HK. Development of Functionalized Capillary-Channeled Polymer (C-CP) Fibers as Stationary Phase for Affinity Chromatography. [Internet] [Doctoral dissertation]. Clemson University; 2019. [cited 2021 Jan 18]. Available from: https://tigerprints.clemson.edu/all_dissertations/2532.

Council of Science Editors:

Trang HK. Development of Functionalized Capillary-Channeled Polymer (C-CP) Fibers as Stationary Phase for Affinity Chromatography. [Doctoral Dissertation]. Clemson University; 2019. Available from: https://tigerprints.clemson.edu/all_dissertations/2532


University of Helsinki

22. Multia, Evgen. Interpreting the biosensor data of biomolecular interactions.

Degree: Department of Chemistry; Helsingfors universitet, Matematisk-naturvetenskapliga fakulteten, Kemiska institutionen, 2017, University of Helsinki

 The literature part of this thesis reviewed the process of obtaining affinity information with quartz crystal microbalance (QCM) and surface plasmon resonance (SPR) biosensors. Basic… (more)

Subjects/Keywords: kinetics; affinity; surface plasmon resonance; quartz crystal microbalance; affinity chromatography; antibody; capillary electrophoresis; binding studies; thermodynamics; partially filling affinity capillary electrophoresis; adsorption energy calculations; Analytical Chemistry; Analyyttinen kemia; Analytisk kemi

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APA (6th Edition):

Multia, E. (2017). Interpreting the biosensor data of biomolecular interactions. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/229179

Chicago Manual of Style (16th Edition):

Multia, Evgen. “Interpreting the biosensor data of biomolecular interactions.” 2017. Masters Thesis, University of Helsinki. Accessed January 18, 2021. http://hdl.handle.net/10138/229179.

MLA Handbook (7th Edition):

Multia, Evgen. “Interpreting the biosensor data of biomolecular interactions.” 2017. Web. 18 Jan 2021.

Vancouver:

Multia E. Interpreting the biosensor data of biomolecular interactions. [Internet] [Masters thesis]. University of Helsinki; 2017. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10138/229179.

Council of Science Editors:

Multia E. Interpreting the biosensor data of biomolecular interactions. [Masters Thesis]. University of Helsinki; 2017. Available from: http://hdl.handle.net/10138/229179


Indian Institute of Science

23. Prajapati, Ravindra Singh. Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP.

Degree: PhD, Faculty of Science, 2009, Indian Institute of Science

 Native states of globular proteins typically show stabilization in the range of 5 to 15 kcal/mol with respect to their unfolded states. There has been… (more)

Subjects/Keywords: Proteins; Escherechia Coli; Leucine Binding Protein; Maltose Binding Protein; Ribose Binding Protein; Leucine Valine Binding Protein; Protein Folding; Protein Stability; Periplasmic Binding Protein; Thioredoxin (Trx); Biochemistry

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APA (6th Edition):

Prajapati, R. S. (2009). Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/428

Chicago Manual of Style (16th Edition):

Prajapati, Ravindra Singh. “Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP.” 2009. Doctoral Dissertation, Indian Institute of Science. Accessed January 18, 2021. http://etd.iisc.ac.in/handle/2005/428.

MLA Handbook (7th Edition):

Prajapati, Ravindra Singh. “Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP.” 2009. Web. 18 Jan 2021.

Vancouver:

Prajapati RS. Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2009. [cited 2021 Jan 18]. Available from: http://etd.iisc.ac.in/handle/2005/428.

Council of Science Editors:

Prajapati RS. Thermodynamic Characterization Of Wild Type And Mutants Of The E.coli Periplasmic Binding Proteins LBP, LIVBP, MBP And RBP. [Doctoral Dissertation]. Indian Institute of Science; 2009. Available from: http://etd.iisc.ac.in/handle/2005/428


KTH

24. Larsson, Emma. Calcium-dependent affinity ligands for protein purification.

Degree: Biotechnology and Health (CBH), 2020, KTH

The rapid growth of the biopharmaceutical industry has led to increasing demands on the protein production process. An important aspect is the yield of… (more)

Subjects/Keywords: Purification; Affinity chromatography; Protein A; Z domain; Calcium-dependent; ZCa; Elution; Medical Biotechnology; Medicinsk bioteknologi

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APA (6th Edition):

Larsson, E. (2020). Calcium-dependent affinity ligands for protein purification. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278695

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):

Larsson, Emma. “Calcium-dependent affinity ligands for protein purification.” 2020. Thesis, KTH. Accessed January 18, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278695.

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

MLA Handbook (7th Edition):

Larsson, Emma. “Calcium-dependent affinity ligands for protein purification.” 2020. Web. 18 Jan 2021.

Vancouver:

Larsson E. Calcium-dependent affinity ligands for protein purification. [Internet] [Thesis]. KTH; 2020. [cited 2021 Jan 18]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278695.

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

Council of Science Editors:

Larsson E. Calcium-dependent affinity ligands for protein purification. [Thesis]. KTH; 2020. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278695

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


Virginia Tech

25. Hey, Carolyn McKenzie. Antibody Purification from Tobacco by Protein A Affinity Chromatography.

Degree: MS, Biological Systems Engineering, 2010, Virginia Tech

 Antibodies represent the largest group of biopharmaceuticals. Due to the nature of their clinical applications, they often need to be produced in large quantities. Plants… (more)

Subjects/Keywords: Tobacco; Protein A; Affinity Chromatography; Antibody

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APA (6th Edition):

Hey, C. M. (2010). Antibody Purification from Tobacco by Protein A Affinity Chromatography. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/42645

Chicago Manual of Style (16th Edition):

Hey, Carolyn McKenzie. “Antibody Purification from Tobacco by Protein A Affinity Chromatography.” 2010. Masters Thesis, Virginia Tech. Accessed January 18, 2021. http://hdl.handle.net/10919/42645.

MLA Handbook (7th Edition):

Hey, Carolyn McKenzie. “Antibody Purification from Tobacco by Protein A Affinity Chromatography.” 2010. Web. 18 Jan 2021.

Vancouver:

Hey CM. Antibody Purification from Tobacco by Protein A Affinity Chromatography. [Internet] [Masters thesis]. Virginia Tech; 2010. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10919/42645.

Council of Science Editors:

Hey CM. Antibody Purification from Tobacco by Protein A Affinity Chromatography. [Masters Thesis]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/42645


University of Arkansas

26. Tiwari, Neha. Proteome Based Development of Novel Affinity Tail for Immobilized Metal Affinity Chromatography and Hydrophobic Interaction Chromatography.

Degree: PhD, 2011, University of Arkansas

  At industrial scale, reducing the step in purification and recovery is desired; this not only decreases the cost but also increases the yield. Hydrophobic… (more)

Subjects/Keywords: Applied sciences; Biological sciences; Affinity tails; Chromatography; Protein purification; Molecular Biology; Other Chemical Engineering

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APA (6th Edition):

Tiwari, N. (2011). Proteome Based Development of Novel Affinity Tail for Immobilized Metal Affinity Chromatography and Hydrophobic Interaction Chromatography. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/180

Chicago Manual of Style (16th Edition):

Tiwari, Neha. “Proteome Based Development of Novel Affinity Tail for Immobilized Metal Affinity Chromatography and Hydrophobic Interaction Chromatography.” 2011. Doctoral Dissertation, University of Arkansas. Accessed January 18, 2021. https://scholarworks.uark.edu/etd/180.

MLA Handbook (7th Edition):

Tiwari, Neha. “Proteome Based Development of Novel Affinity Tail for Immobilized Metal Affinity Chromatography and Hydrophobic Interaction Chromatography.” 2011. Web. 18 Jan 2021.

Vancouver:

Tiwari N. Proteome Based Development of Novel Affinity Tail for Immobilized Metal Affinity Chromatography and Hydrophobic Interaction Chromatography. [Internet] [Doctoral dissertation]. University of Arkansas; 2011. [cited 2021 Jan 18]. Available from: https://scholarworks.uark.edu/etd/180.

Council of Science Editors:

Tiwari N. Proteome Based Development of Novel Affinity Tail for Immobilized Metal Affinity Chromatography and Hydrophobic Interaction Chromatography. [Doctoral Dissertation]. University of Arkansas; 2011. Available from: https://scholarworks.uark.edu/etd/180

27. Kekule Vithanage, Thamarasi Vithana. Identifying Lead Compounds for S100P in Pancreatic Cancer Therapy Using in Vitro Biophysical Techniques.

Degree: 2016, University of Hertfordshire

 The protein S100P has been associated with the aggressiveness of several neoplastic disease, including pancreatic ductal adenocarcinoma (PDAC). S100 proteins are a family of calcium… (more)

Subjects/Keywords: S100 proteins; Ca2+ binding proteins; S100P; Receptor for Advanced Glycation End Products (RAGE); mitogen-activated protein kinase (MAPK); S100P-RAGE complex; Pancreatic cancer; Affinity chromatography; Sodium dodecyl sulphate (SDS); polyacrylamide gel electrophoresis (PAGE); Nuclear Magnetic Resonance (NMR) spectroscopy

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APA (6th Edition):

Kekule Vithanage, T. V. (2016). Identifying Lead Compounds for S100P in Pancreatic Cancer Therapy Using in Vitro Biophysical Techniques. (Masters Thesis). University of Hertfordshire. Retrieved from http://hdl.handle.net/2299/22629

Chicago Manual of Style (16th Edition):

Kekule Vithanage, Thamarasi Vithana. “Identifying Lead Compounds for S100P in Pancreatic Cancer Therapy Using in Vitro Biophysical Techniques.” 2016. Masters Thesis, University of Hertfordshire. Accessed January 18, 2021. http://hdl.handle.net/2299/22629.

MLA Handbook (7th Edition):

Kekule Vithanage, Thamarasi Vithana. “Identifying Lead Compounds for S100P in Pancreatic Cancer Therapy Using in Vitro Biophysical Techniques.” 2016. Web. 18 Jan 2021.

Vancouver:

Kekule Vithanage TV. Identifying Lead Compounds for S100P in Pancreatic Cancer Therapy Using in Vitro Biophysical Techniques. [Internet] [Masters thesis]. University of Hertfordshire; 2016. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/2299/22629.

Council of Science Editors:

Kekule Vithanage TV. Identifying Lead Compounds for S100P in Pancreatic Cancer Therapy Using in Vitro Biophysical Techniques. [Masters Thesis]. University of Hertfordshire; 2016. Available from: http://hdl.handle.net/2299/22629


Uppsala University

28. Lecaros, Luis Sanchez. Cloning and expression of superoxide dismutase from Sarcoptes scabiei in Escherichia coli.

Degree: Medical Biochemistry and Microbiology, 2006, Uppsala University

  Sarcoptes scabiei is a disease-causing parasitic mite of humans and animals that is prevalent worldwide. The parasite lives in burrows in the epidermis of… (more)

Subjects/Keywords: recombinant protein; SOD; maltose binding protein; his-tag; defence; Microbiology; Mikrobiologi

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APA (6th Edition):

Lecaros, L. S. (2006). Cloning and expression of superoxide dismutase from Sarcoptes scabiei in Escherichia coli. (Thesis). Uppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7428

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):

Lecaros, Luis Sanchez. “Cloning and expression of superoxide dismutase from Sarcoptes scabiei in Escherichia coli.” 2006. Thesis, Uppsala University. Accessed January 18, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7428.

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

MLA Handbook (7th Edition):

Lecaros, Luis Sanchez. “Cloning and expression of superoxide dismutase from Sarcoptes scabiei in Escherichia coli.” 2006. Web. 18 Jan 2021.

Vancouver:

Lecaros LS. Cloning and expression of superoxide dismutase from Sarcoptes scabiei in Escherichia coli. [Internet] [Thesis]. Uppsala University; 2006. [cited 2021 Jan 18]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7428.

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

Council of Science Editors:

Lecaros LS. Cloning and expression of superoxide dismutase from Sarcoptes scabiei in Escherichia coli. [Thesis]. Uppsala University; 2006. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7428

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


University of California – Riverside

29. Deans, Jonathan R. The Role of Nuclear Receptors in Tissue-Specific Gene Expression: The Impact of Genetic Variation on DNA Binding.

Degree: Genetics, Genomics and Bioinformatics, 2017, University of California – Riverside

 Nuclear receptors (NRs) are ligand-sensitive transcription factors that regulate a wide array of biological processes including development, metabolism, and circadian rhythms. All NRs share a… (more)

Subjects/Keywords: Bioinformatics; Affinity altering SNPs; Alternative promoters; Lipid metabolism; Nuclear receptors; Protein binding microarrays

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

APA (6th Edition):

Deans, J. R. (2017). The Role of Nuclear Receptors in Tissue-Specific Gene Expression: The Impact of Genetic Variation on DNA Binding. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/2cw7q5hj

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):

Deans, Jonathan R. “The Role of Nuclear Receptors in Tissue-Specific Gene Expression: The Impact of Genetic Variation on DNA Binding.” 2017. Thesis, University of California – Riverside. Accessed January 18, 2021. http://www.escholarship.org/uc/item/2cw7q5hj.

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

MLA Handbook (7th Edition):

Deans, Jonathan R. “The Role of Nuclear Receptors in Tissue-Specific Gene Expression: The Impact of Genetic Variation on DNA Binding.” 2017. Web. 18 Jan 2021.

Vancouver:

Deans JR. The Role of Nuclear Receptors in Tissue-Specific Gene Expression: The Impact of Genetic Variation on DNA Binding. [Internet] [Thesis]. University of California – Riverside; 2017. [cited 2021 Jan 18]. Available from: http://www.escholarship.org/uc/item/2cw7q5hj.

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

Council of Science Editors:

Deans JR. The Role of Nuclear Receptors in Tissue-Specific Gene Expression: The Impact of Genetic Variation on DNA Binding. [Thesis]. University of California – Riverside; 2017. Available from: http://www.escholarship.org/uc/item/2cw7q5hj

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


Queens University

30. Vanderveer, Tara Lynn. The function, characterization of expression, localization and activity of a divergent ice nucleating protein from Pseudomonas borealis .

Degree: Biology, 2012, Queens University

 An ice nucleating protein (INP) with 66% amino acid sequence identity to the better-known INP of Pseudomonas syringae has been described in an environmental isolate… (more)

Subjects/Keywords: Ice Nucleating Protein ; Ice Binding Proteins ; Ice Affinity ; Fluorescence Microscopy ; Pseudomonas Borealis

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

APA (6th Edition):

Vanderveer, T. L. (2012). The function, characterization of expression, localization and activity of a divergent ice nucleating protein from Pseudomonas borealis . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/7200

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):

Vanderveer, Tara Lynn. “The function, characterization of expression, localization and activity of a divergent ice nucleating protein from Pseudomonas borealis .” 2012. Thesis, Queens University. Accessed January 18, 2021. http://hdl.handle.net/1974/7200.

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

MLA Handbook (7th Edition):

Vanderveer, Tara Lynn. “The function, characterization of expression, localization and activity of a divergent ice nucleating protein from Pseudomonas borealis .” 2012. Web. 18 Jan 2021.

Vancouver:

Vanderveer TL. The function, characterization of expression, localization and activity of a divergent ice nucleating protein from Pseudomonas borealis . [Internet] [Thesis]. Queens University; 2012. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1974/7200.

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

Council of Science Editors:

Vanderveer TL. The function, characterization of expression, localization and activity of a divergent ice nucleating protein from Pseudomonas borealis . [Thesis]. Queens University; 2012. Available from: http://hdl.handle.net/1974/7200

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

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