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You searched for subject:(peptide purification). Showing records 1 – 21 of 21 total matches.

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Massey University

1. Sugiarto, Haryadi. Isolation and characterisation of host defence peptides ostricacins from ostrich heterophils.

Degree: Masterate of Technology, Biotechnology, 2006, Massey University

 Host defence peptides are ubiquitous components of innate immunity within all living organisms. These peptides are small, positively charged and amphiphilic molecules. The biological roles… (more)

Subjects/Keywords: Peptide antibiotics; Blood proteins  – Purification; Ostriches

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APA (6th Edition):

Sugiarto, H. (2006). Isolation and characterisation of host defence peptides ostricacins from ostrich heterophils. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/13173

Chicago Manual of Style (16th Edition):

Sugiarto, Haryadi. “Isolation and characterisation of host defence peptides ostricacins from ostrich heterophils.” 2006. Masters Thesis, Massey University. Accessed July 16, 2019. http://hdl.handle.net/10179/13173.

MLA Handbook (7th Edition):

Sugiarto, Haryadi. “Isolation and characterisation of host defence peptides ostricacins from ostrich heterophils.” 2006. Web. 16 Jul 2019.

Vancouver:

Sugiarto H. Isolation and characterisation of host defence peptides ostricacins from ostrich heterophils. [Internet] [Masters thesis]. Massey University; 2006. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10179/13173.

Council of Science Editors:

Sugiarto H. Isolation and characterisation of host defence peptides ostricacins from ostrich heterophils. [Masters Thesis]. Massey University; 2006. Available from: http://hdl.handle.net/10179/13173


University of Florida

2. Biswas, Suvendu. Strategic Synthesis of Peptides, Labeled Peptides and Peptidomimetics.

Degree: PhD, Chemistry, 2014, University of Florida

 The theme of the current work is the design and development of strategicmethodologies for the synthesis of variety of peptide and peptide-like organic compounds. Chapter… (more)

Subjects/Keywords: Amino acids; Chemicals; Coumarins; Esters; Hydrochlorides; Ligation; Microcrystals; Peptidomimetics; Purification; Solvents; labeling  – peptide  – peptidomimetics

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APA (6th Edition):

Biswas, S. (2014). Strategic Synthesis of Peptides, Labeled Peptides and Peptidomimetics. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0046517

Chicago Manual of Style (16th Edition):

Biswas, Suvendu. “Strategic Synthesis of Peptides, Labeled Peptides and Peptidomimetics.” 2014. Doctoral Dissertation, University of Florida. Accessed July 16, 2019. http://ufdc.ufl.edu/UFE0046517.

MLA Handbook (7th Edition):

Biswas, Suvendu. “Strategic Synthesis of Peptides, Labeled Peptides and Peptidomimetics.” 2014. Web. 16 Jul 2019.

Vancouver:

Biswas S. Strategic Synthesis of Peptides, Labeled Peptides and Peptidomimetics. [Internet] [Doctoral dissertation]. University of Florida; 2014. [cited 2019 Jul 16]. Available from: http://ufdc.ufl.edu/UFE0046517.

Council of Science Editors:

Biswas S. Strategic Synthesis of Peptides, Labeled Peptides and Peptidomimetics. [Doctoral Dissertation]. University of Florida; 2014. Available from: http://ufdc.ufl.edu/UFE0046517


University of Arkansas

3. Mukherjee, Rudra Palash. Cloning, Fed-Batch Expression And Purification Of A Novel Anti-Candida Peptide And Development Of A Cleavage Resistant Variant Of Green Fluorescence Protein.

Degree: PhD, 2016, University of Arkansas

  This work illustrates that the intelligent design of a bioprocess for the production of peptides of various length is possible by having a prior… (more)

Subjects/Keywords: Pure sciences; Applied sciences; Antifungal peptide; Bio processing; Chromatography; Fed batch; Fermentation; Purification; Biochemical and Biomolecular Engineering

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APA (6th Edition):

Mukherjee, R. P. (2016). Cloning, Fed-Batch Expression And Purification Of A Novel Anti-Candida Peptide And Development Of A Cleavage Resistant Variant Of Green Fluorescence Protein. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/1597

Chicago Manual of Style (16th Edition):

Mukherjee, Rudra Palash. “Cloning, Fed-Batch Expression And Purification Of A Novel Anti-Candida Peptide And Development Of A Cleavage Resistant Variant Of Green Fluorescence Protein.” 2016. Doctoral Dissertation, University of Arkansas. Accessed July 16, 2019. https://scholarworks.uark.edu/etd/1597.

MLA Handbook (7th Edition):

Mukherjee, Rudra Palash. “Cloning, Fed-Batch Expression And Purification Of A Novel Anti-Candida Peptide And Development Of A Cleavage Resistant Variant Of Green Fluorescence Protein.” 2016. Web. 16 Jul 2019.

Vancouver:

Mukherjee RP. Cloning, Fed-Batch Expression And Purification Of A Novel Anti-Candida Peptide And Development Of A Cleavage Resistant Variant Of Green Fluorescence Protein. [Internet] [Doctoral dissertation]. University of Arkansas; 2016. [cited 2019 Jul 16]. Available from: https://scholarworks.uark.edu/etd/1597.

Council of Science Editors:

Mukherjee RP. Cloning, Fed-Batch Expression And Purification Of A Novel Anti-Candida Peptide And Development Of A Cleavage Resistant Variant Of Green Fluorescence Protein. [Doctoral Dissertation]. University of Arkansas; 2016. Available from: https://scholarworks.uark.edu/etd/1597


University of Melbourne

4. Rimmer, Kieran. Structural perspectives on mitochondrial import across the outer membrane.

Degree: 2010, University of Melbourne

 The mitochondrion is an essential organelle in the eukaryotic cell, mediating functions as diverse as oxidative phosphorylation and apoptosis. The mitochondrion, which was once a… (more)

Subjects/Keywords: NMR; nuclear magnetic resonance; protein structure; mitochondrial import; import; peptide expression; peptide purification; peptide structure; spin label; paramagnetic; protein-peptide interactions; cyanogen bromide; CNBr; Tom20; Tom22; presequence; preprotein; mitochondrial outer membrane; Translocase

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APA (6th Edition):

Rimmer, K. (2010). Structural perspectives on mitochondrial import across the outer membrane. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/35457

Chicago Manual of Style (16th Edition):

Rimmer, Kieran. “Structural perspectives on mitochondrial import across the outer membrane.” 2010. Doctoral Dissertation, University of Melbourne. Accessed July 16, 2019. http://hdl.handle.net/11343/35457.

MLA Handbook (7th Edition):

Rimmer, Kieran. “Structural perspectives on mitochondrial import across the outer membrane.” 2010. Web. 16 Jul 2019.

Vancouver:

Rimmer K. Structural perspectives on mitochondrial import across the outer membrane. [Internet] [Doctoral dissertation]. University of Melbourne; 2010. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/11343/35457.

Council of Science Editors:

Rimmer K. Structural perspectives on mitochondrial import across the outer membrane. [Doctoral Dissertation]. University of Melbourne; 2010. Available from: http://hdl.handle.net/11343/35457


Université de Montréal

5. Viau, Martin. Synthèse et caractérisation physicochimique de peptides de polyglutamines .

Degree: 2011, Université de Montréal

 Neuf maladies neurodégénératives sont le produit de l’expression de gènes mutés, dans lesquels le codon CAG est répété au-delà d’un seuil pathologique. Ceci produit des… (more)

Subjects/Keywords: Polyglutamine; Peptide; Synthèse sur phase solide; Solubilisation; Agrégation; Spectroscopie; Microscopie; Diffusion de la lumière; Neurodégénération; Solid-phase synthesis; Solubilization; Aggregation; Spectroscopy; Light scattering; Neurodegeneration; Purification; Microscopy

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APA (6th Edition):

Viau, M. (2011). Synthèse et caractérisation physicochimique de peptides de polyglutamines . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6090

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):

Viau, Martin. “Synthèse et caractérisation physicochimique de peptides de polyglutamines .” 2011. Thesis, Université de Montréal. Accessed July 16, 2019. http://hdl.handle.net/1866/6090.

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

MLA Handbook (7th Edition):

Viau, Martin. “Synthèse et caractérisation physicochimique de peptides de polyglutamines .” 2011. Web. 16 Jul 2019.

Vancouver:

Viau M. Synthèse et caractérisation physicochimique de peptides de polyglutamines . [Internet] [Thesis]. Université de Montréal; 2011. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1866/6090.

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

Council of Science Editors:

Viau M. Synthèse et caractérisation physicochimique de peptides de polyglutamines . [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/6090

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


University of Victoria

6. Jantzen, Roni Rebecca. Expression of human α-N-Acetylglucosaminidase in Sf9 insect cells: effect of cryptic splice site removal and native secretion-signaling peptide addition.

Degree: Dept. of Biology, 2011, University of Victoria

 Human α-N-Acetylglucosaminidase (Naglu) is a lysosomal acid hydrolase implicated in tthe rare metabolic storage disorder known as mucopolysaccharidosis type IIIB (MPS IIIB; also Sanfilippo syndrome… (more)

Subjects/Keywords: α-N-Acetylglucosaminidase; Sf9; insect cells; secretion signal peptide; lysosomal enzyme; mucopolysaccharidosis; MPS IIIB; sanfilippo syndrome; protein expression; protein transduction domain; splice site; cryptic splicing; site-directed mutagenesis; Naglu; cDNA; protein purification; hydrophobic interaction chromatography; FPLC; recombinant human protein; fusion protein; Tat-PTD

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APA (6th Edition):

Jantzen, R. R. (2011). Expression of human α-N-Acetylglucosaminidase in Sf9 insect cells: effect of cryptic splice site removal and native secretion-signaling peptide addition. (Masters Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/3455

Chicago Manual of Style (16th Edition):

Jantzen, Roni Rebecca. “Expression of human α-N-Acetylglucosaminidase in Sf9 insect cells: effect of cryptic splice site removal and native secretion-signaling peptide addition.” 2011. Masters Thesis, University of Victoria. Accessed July 16, 2019. http://hdl.handle.net/1828/3455.

MLA Handbook (7th Edition):

Jantzen, Roni Rebecca. “Expression of human α-N-Acetylglucosaminidase in Sf9 insect cells: effect of cryptic splice site removal and native secretion-signaling peptide addition.” 2011. Web. 16 Jul 2019.

Vancouver:

Jantzen RR. Expression of human α-N-Acetylglucosaminidase in Sf9 insect cells: effect of cryptic splice site removal and native secretion-signaling peptide addition. [Internet] [Masters thesis]. University of Victoria; 2011. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1828/3455.

Council of Science Editors:

Jantzen RR. Expression of human α-N-Acetylglucosaminidase in Sf9 insect cells: effect of cryptic splice site removal and native secretion-signaling peptide addition. [Masters Thesis]. University of Victoria; 2011. Available from: http://hdl.handle.net/1828/3455


ETH Zürich

7. Münchbach, Martin Christian. Development of tools for proteome analysis.

Degree: 1999, ETH Zürich

Subjects/Keywords: PROTEOM (PROTEINE UND PEPTIDE); METHODIK UND TECHNIKEN FÜR PROTEINE UND PEPTIDE; TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; PROTEINANALYTIK + PEPTIDANALYTIK (BIOCHEMIE); PROTEOME (PROTEINS AND PEPTIDES); METHODS AND TECHNIQUES FOR PROTEINS AND PEPTIDES; SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; PROTEIN ANALYSIS + PEPTIDE ANALYSIS (BIOCHEMISTRY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Münchbach, M. C. (1999). Development of tools for proteome analysis. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/144289

Chicago Manual of Style (16th Edition):

Münchbach, Martin Christian. “Development of tools for proteome analysis.” 1999. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/144289.

MLA Handbook (7th Edition):

Münchbach, Martin Christian. “Development of tools for proteome analysis.” 1999. Web. 16 Jul 2019.

Vancouver:

Münchbach MC. Development of tools for proteome analysis. [Internet] [Doctoral dissertation]. ETH Zürich; 1999. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/144289.

Council of Science Editors:

Münchbach MC. Development of tools for proteome analysis. [Doctoral Dissertation]. ETH Zürich; 1999. Available from: http://hdl.handle.net/20.500.11850/144289


ETH Zürich

8. Mijuskovic, Martina. Structural and biochemical studies on human TAF2.

Degree: 2007, ETH Zürich

 Eukaryotes have thousands of genes whose expressionmust be tightly regulated to ensure the organism's survival, growth and development. Synthesis of messenger RNA, a process known… (more)

Subjects/Keywords: TRANSCRIPTION FACTORS (MOLECULAR GENETICS); TRANSKRIPTIONSFAKTOREN (MOLEKULARE GENETIK); PROTEIN FUNCTION + PEPTIDE FUNCTION; PROTEINFUNKTION + PEPTIDFUNKTION; SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Mijuskovic, M. (2007). Structural and biochemical studies on human TAF2. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/5593

Chicago Manual of Style (16th Edition):

Mijuskovic, Martina. “Structural and biochemical studies on human TAF2.” 2007. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/5593.

MLA Handbook (7th Edition):

Mijuskovic, Martina. “Structural and biochemical studies on human TAF2.” 2007. Web. 16 Jul 2019.

Vancouver:

Mijuskovic M. Structural and biochemical studies on human TAF2. [Internet] [Doctoral dissertation]. ETH Zürich; 2007. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/5593.

Council of Science Editors:

Mijuskovic M. Structural and biochemical studies on human TAF2. [Doctoral Dissertation]. ETH Zürich; 2007. Available from: http://hdl.handle.net/20.500.11850/5593


ETH Zürich

9. Wyler, Emanuel. Tandem affinity purification combined with inducible shRNA expression as a tool to study the maturation of macromolecular assemblies.

Degree: 2010, ETH Zürich

Subjects/Keywords: BIOSYNTHESE UND ZUSAMMENLAGERUNG DER RIBOSOMEN; HUMANCYTOLOGIE + MENSCHLICHE ZELLEN (BIOLOGIE); TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; PROTEINFUNKTION + PEPTIDFUNKTION; BIOSYNTHESIS AND ASSEMBLY OF RIBOSOMES; HUMAN CYTOLOGY + HUMAN CELLS (BIOLOGY); SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; PROTEIN FUNCTION + PEPTIDE FUNCTION; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Wyler, E. (2010). Tandem affinity purification combined with inducible shRNA expression as a tool to study the maturation of macromolecular assemblies. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/152373

Chicago Manual of Style (16th Edition):

Wyler, Emanuel. “Tandem affinity purification combined with inducible shRNA expression as a tool to study the maturation of macromolecular assemblies.” 2010. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/152373.

MLA Handbook (7th Edition):

Wyler, Emanuel. “Tandem affinity purification combined with inducible shRNA expression as a tool to study the maturation of macromolecular assemblies.” 2010. Web. 16 Jul 2019.

Vancouver:

Wyler E. Tandem affinity purification combined with inducible shRNA expression as a tool to study the maturation of macromolecular assemblies. [Internet] [Doctoral dissertation]. ETH Zürich; 2010. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/152373.

Council of Science Editors:

Wyler E. Tandem affinity purification combined with inducible shRNA expression as a tool to study the maturation of macromolecular assemblies. [Doctoral Dissertation]. ETH Zürich; 2010. Available from: http://hdl.handle.net/20.500.11850/152373


ETH Zürich

10. Hoving, Sjouke. A novel method for N-terminal ladder sequencing and subtractive proteome analysis of Oocytes from Asterina pectinifera after resumption of meiosis.

Degree: 1998, ETH Zürich

Subjects/Keywords: TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; PROTEOM (PROTEINE UND PEPTIDE); POLYACRYLAMIDGELELEKTROPHORESE; GELELEKTROPHORESE (BIOLOGIE); EIZELLEN (EMBRYOLOGIE); ASTERIIDAE (ZOOLOGIE); SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; PROTEOME (PROTEINS AND PEPTIDES); POLYACRYLAMID GEL ELECTROPHORESIS; GEL ELECTROPHORESIS (BIOLOGY); EGGS (EMBRYOLOGY); ASTERIIDAE (ZOOLOGY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Hoving, S. (1998). A novel method for N-terminal ladder sequencing and subtractive proteome analysis of Oocytes from Asterina pectinifera after resumption of meiosis. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/143878

Chicago Manual of Style (16th Edition):

Hoving, Sjouke. “A novel method for N-terminal ladder sequencing and subtractive proteome analysis of Oocytes from Asterina pectinifera after resumption of meiosis.” 1998. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/143878.

MLA Handbook (7th Edition):

Hoving, Sjouke. “A novel method for N-terminal ladder sequencing and subtractive proteome analysis of Oocytes from Asterina pectinifera after resumption of meiosis.” 1998. Web. 16 Jul 2019.

Vancouver:

Hoving S. A novel method for N-terminal ladder sequencing and subtractive proteome analysis of Oocytes from Asterina pectinifera after resumption of meiosis. [Internet] [Doctoral dissertation]. ETH Zürich; 1998. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/143878.

Council of Science Editors:

Hoving S. A novel method for N-terminal ladder sequencing and subtractive proteome analysis of Oocytes from Asterina pectinifera after resumption of meiosis. [Doctoral Dissertation]. ETH Zürich; 1998. Available from: http://hdl.handle.net/20.500.11850/143878


University of Florida

11. Carter, John Mark, 1962-. Assessment of binding domains of mouse interferon gamma using synthetic peptides and antibodies.

Degree: 1987, University of Florida

Subjects/Keywords: Amino acids; Antibodies; Epitopes; Gels; Interferons; Molecules; Monoclonal antibodies; Proteins; Purification; Receptors; Binding Sites, Antibody ( mesh ); Biochemistry and Molecular Biology thesis Ph.D ( mesh ); Interferon-gamma, Recombinant ( mesh ); Peptide Termination Factors ( mesh )

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APA (6th Edition):

Carter, John Mark, 1. (1987). Assessment of binding domains of mouse interferon gamma using synthetic peptides and antibodies. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00055800

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):

Carter, John Mark, 1962-. “Assessment of binding domains of mouse interferon gamma using synthetic peptides and antibodies.” 1987. Thesis, University of Florida. Accessed July 16, 2019. http://ufdc.ufl.edu/AA00055800.

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

MLA Handbook (7th Edition):

Carter, John Mark, 1962-. “Assessment of binding domains of mouse interferon gamma using synthetic peptides and antibodies.” 1987. Web. 16 Jul 2019.

Vancouver:

Carter, John Mark 1. Assessment of binding domains of mouse interferon gamma using synthetic peptides and antibodies. [Internet] [Thesis]. University of Florida; 1987. [cited 2019 Jul 16]. Available from: http://ufdc.ufl.edu/AA00055800.

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

Council of Science Editors:

Carter, John Mark 1. Assessment of binding domains of mouse interferon gamma using synthetic peptides and antibodies. [Thesis]. University of Florida; 1987. Available from: http://ufdc.ufl.edu/AA00055800

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


Universitat Pompeu Fabra

12. Such Sanmartin, Gerard. Assessing human growth hormone variants to determine their potential relevance in anti-doping and clinical analysis.

Degree: Departament de Ciències Experimentals i de la Salut, 2010, Universitat Pompeu Fabra

 L'hormona de creixement humana (GH) participa en el creixement post-longitudinal i en el metabolisme de lípids i carbohidrats, i comprèn un extraordinari nombre de proteïnes… (more)

Subjects/Keywords: amplificació de senyal; superficial; ressonància de plasmó; caracterització d'anticossos; anticossos; anticossos anti-GH; dicroisme circular; síntesi en fase sòlida; thermolisinòlisis; thermolisina; purificació; generació; fragmentació de pèptids; fragmentació de proteïnes; proteòlisis limitada; GH44-191; GH1-191; 22 kDa; GH1-43; 20 kDa; 17 kDa; 5 kDa; humana; fragments de la hormona de creixement humana; isoformes de la hormona de creixement; variants de la hormona de creixement humana; Hormona de creixement humana; protocol; C-reactive protein; mannanbinding lectin; serum purification; blood purification; MALDI; mass spectrometry; western blot; immunoassay; SPR-based method; signal enhancement; surface plasmon resonance; anti-GH antibodies; characterisation of antibodies; antibodies; circular dichroism; solid phase synthesis; thermolysinolysis; thermolysin; generation; purification; fragmentation; peptide; protein fragmentation; mètode basat en SPR; limited proteolysis; GH1-191; GH44-191; GH1-43; 22 kDa; 20 kDa; 17 kDa; 5 kDa; human growth hormone fragments; human growth hormone isoforms; human growth hormone variants; Human growth hormone; immunoassaig; western blot; MALDI; espectrometria de massa; purificació de sang; purificació de sèrum; proteïna C-reactiva; mannan binding lectin; protocol; 57; 61

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APA (6th Edition):

Such Sanmartin, G. (2010). Assessing human growth hormone variants to determine their potential relevance in anti-doping and clinical analysis. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/7198

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):

Such Sanmartin, Gerard. “Assessing human growth hormone variants to determine their potential relevance in anti-doping and clinical analysis.” 2010. Thesis, Universitat Pompeu Fabra. Accessed July 16, 2019. http://hdl.handle.net/10803/7198.

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

MLA Handbook (7th Edition):

Such Sanmartin, Gerard. “Assessing human growth hormone variants to determine their potential relevance in anti-doping and clinical analysis.” 2010. Web. 16 Jul 2019.

Vancouver:

Such Sanmartin G. Assessing human growth hormone variants to determine their potential relevance in anti-doping and clinical analysis. [Internet] [Thesis]. Universitat Pompeu Fabra; 2010. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10803/7198.

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

Council of Science Editors:

Such Sanmartin G. Assessing human growth hormone variants to determine their potential relevance in anti-doping and clinical analysis. [Thesis]. Universitat Pompeu Fabra; 2010. Available from: http://hdl.handle.net/10803/7198

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


ETH Zürich

13. Yong, Tze F. Crosslinking and Purification of ISW1a(∆ATPase)-45N0 Nucleosome Complex for Crystallisation Studies.

Degree: 2015, ETH Zürich

Subjects/Keywords: NUKLEOSOMEN (CYTOLOGIE); CRYSTAL STRUCTURES OF PROTEINS AND PEPTIDES; THREE-DIMENSIONAL PROTEIN AND PEPTIDE STRUCTURE, PROTEIN AND PEPTIDE CONFORMATION; NUCLEOSOMES (CYTOLOGY); CHROMATIN STRUCTURE (CYTOLOGY); PROTEIN COMPLEXES; RÄUMLICHE PROTEIN- UND PEPTIDSTRUKTUR, PROTEIN- UND PEPTIDKONFORMATION; KRISTALLSTRUKTUREN VON PROTEINEN UND PEPTIDEN; CHROMATINSTRUKTUR (CYTOLOGIE); PROTEINKOMPLEXE; SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; ATPASEN (ENZYME); ATPASES (ENZYMES); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Yong, T. F. (2015). Crosslinking and Purification of ISW1a(∆ATPase)-45N0 Nucleosome Complex for Crystallisation Studies. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/111659

Chicago Manual of Style (16th Edition):

Yong, Tze F. “Crosslinking and Purification of ISW1a(∆ATPase)-45N0 Nucleosome Complex for Crystallisation Studies.” 2015. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/111659.

MLA Handbook (7th Edition):

Yong, Tze F. “Crosslinking and Purification of ISW1a(∆ATPase)-45N0 Nucleosome Complex for Crystallisation Studies.” 2015. Web. 16 Jul 2019.

Vancouver:

Yong TF. Crosslinking and Purification of ISW1a(∆ATPase)-45N0 Nucleosome Complex for Crystallisation Studies. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/111659.

Council of Science Editors:

Yong TF. Crosslinking and Purification of ISW1a(∆ATPase)-45N0 Nucleosome Complex for Crystallisation Studies. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/111659


ETH Zürich

14. Zelenay, Viviane. Development of a Purification Protocol for CRF Receptor Isomers and a Structural Investigations of a Potential Interaction Between Nogo-A-20 and S1PR2-Fragments.

Degree: 2015, ETH Zürich

Subjects/Keywords: G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; PROTEINISOLIERUNG + PROTEINPRÄPARATION + PEPTIDISOLIERUNG + PEPTIDPRÄPARATION (BIOLOGISCHE TECHNIKEN); AFFINITÄTSCHROMATOGRAPHIE (BIOLOGIE); KERNRESONANZSPEKTROSKOPIE; MEMBRANPROTEINSTRUKTUR; G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; PROTEIN ISOLATION + PROTEIN PREPARATION + PEPTIDE ISOLATION + PEPTIDE PREPARATION (BIOLOGICAL TECHNIQUES); AFFINITY CHROMATOGRAPHY (BIOLOGY); NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; MEMBRANE PROTEIN STRUCTURE; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Zelenay, V. (2015). Development of a Purification Protocol for CRF Receptor Isomers and a Structural Investigations of a Potential Interaction Between Nogo-A-20 and S1PR2-Fragments. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155106

Chicago Manual of Style (16th Edition):

Zelenay, Viviane. “Development of a Purification Protocol for CRF Receptor Isomers and a Structural Investigations of a Potential Interaction Between Nogo-A-20 and S1PR2-Fragments.” 2015. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/155106.

MLA Handbook (7th Edition):

Zelenay, Viviane. “Development of a Purification Protocol for CRF Receptor Isomers and a Structural Investigations of a Potential Interaction Between Nogo-A-20 and S1PR2-Fragments.” 2015. Web. 16 Jul 2019.

Vancouver:

Zelenay V. Development of a Purification Protocol for CRF Receptor Isomers and a Structural Investigations of a Potential Interaction Between Nogo-A-20 and S1PR2-Fragments. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/155106.

Council of Science Editors:

Zelenay V. Development of a Purification Protocol for CRF Receptor Isomers and a Structural Investigations of a Potential Interaction Between Nogo-A-20 and S1PR2-Fragments. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/155106


ETH Zürich

15. Möller, Dirk Björn. Acoustically driven particle transport in fluid chambers.

Degree: 2013, ETH Zürich

Subjects/Keywords: MICROFLUIDICS AND NANOFLUIDICS; LAB-ON-A-CHIP; MIKROFLUIDIK UND NANOFLUIDIK; SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; ULTRASONICS (ACOUSTICS); ULTRASCHALL (AKUSTIK); info:eu-repo/classification/ddc/530; info:eu-repo/classification/ddc/621.3; Physics; Electric engineering

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APA (6th Edition):

Möller, D. B. (2013). Acoustically driven particle transport in fluid chambers. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/80554

Chicago Manual of Style (16th Edition):

Möller, Dirk Björn. “Acoustically driven particle transport in fluid chambers.” 2013. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/80554.

MLA Handbook (7th Edition):

Möller, Dirk Björn. “Acoustically driven particle transport in fluid chambers.” 2013. Web. 16 Jul 2019.

Vancouver:

Möller DB. Acoustically driven particle transport in fluid chambers. [Internet] [Doctoral dissertation]. ETH Zürich; 2013. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/80554.

Council of Science Editors:

Möller DB. Acoustically driven particle transport in fluid chambers. [Doctoral Dissertation]. ETH Zürich; 2013. Available from: http://hdl.handle.net/20.500.11850/80554


ETH Zürich

16. Angarita Velasquez, Monica J. Purification of recombinant proteins using batch and semi-continuous chromatography.

Degree: 2014, ETH Zürich

Subjects/Keywords: HYBRIDPROTEINE + REKOMBINANTE PROTEINE; PREPARATIVE CHROMATOGRAPHY; GEGENSTROMVERTEILUNGSCHROMATOGRAPHIE; PRÄPARATIVE CHROMATOGRAPHIE; COUNTERCURRENT DISTRIBUTION CHROMATOGRAPHY; HYBRID PROTEINS + RECOMBINANT PROTEINS; SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Angarita Velasquez, M. J. (2014). Purification of recombinant proteins using batch and semi-continuous chromatography. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/92108

Chicago Manual of Style (16th Edition):

Angarita Velasquez, Monica J. “Purification of recombinant proteins using batch and semi-continuous chromatography.” 2014. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/92108.

MLA Handbook (7th Edition):

Angarita Velasquez, Monica J. “Purification of recombinant proteins using batch and semi-continuous chromatography.” 2014. Web. 16 Jul 2019.

Vancouver:

Angarita Velasquez MJ. Purification of recombinant proteins using batch and semi-continuous chromatography. [Internet] [Doctoral dissertation]. ETH Zürich; 2014. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/92108.

Council of Science Editors:

Angarita Velasquez MJ. Purification of recombinant proteins using batch and semi-continuous chromatography. [Doctoral Dissertation]. ETH Zürich; 2014. Available from: http://hdl.handle.net/20.500.11850/92108


ETH Zürich

17. Steinebach, Fabian. Multi-Column Chromatography for Continuous Integrated Biomanufacturing.

Degree: 2017, ETH Zürich

Subjects/Keywords: AFFINITY CHROMATOGRAPHY (BIOLOGY); PROTEIN ENGINEERING + ENZYME ENGINEERING; OPTIMIERUNG (VERFAHRENSTECHNIK); BIOPROCESS ENGINEERING (BIOTECHNOLOGY); AFFINITÄTSCHROMATOGRAPHIE (BIOLOGIE); MONOCLONAL ANTIBODIES (IMMUNOLOGICAL TECHNIQUES); BIOVERFAHRENSTECHNIK (BIOTECHNOLOGIE); MONOKLONALE ANTIKÖRPER (IMMUNOLOGISCHE TECHNIKEN); PROTEINBIOTECHNOLOGIE + ENZYMBIOTECHNOLOGIE; SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; OPTIMIZATION/PROCESS ENGINEERING; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Steinebach, F. (2017). Multi-Column Chromatography for Continuous Integrated Biomanufacturing. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/129513

Chicago Manual of Style (16th Edition):

Steinebach, Fabian. “Multi-Column Chromatography for Continuous Integrated Biomanufacturing.” 2017. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/129513.

MLA Handbook (7th Edition):

Steinebach, Fabian. “Multi-Column Chromatography for Continuous Integrated Biomanufacturing.” 2017. Web. 16 Jul 2019.

Vancouver:

Steinebach F. Multi-Column Chromatography for Continuous Integrated Biomanufacturing. [Internet] [Doctoral dissertation]. ETH Zürich; 2017. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/129513.

Council of Science Editors:

Steinebach F. Multi-Column Chromatography for Continuous Integrated Biomanufacturing. [Doctoral Dissertation]. ETH Zürich; 2017. Available from: http://hdl.handle.net/20.500.11850/129513


ETH Zürich

18. Wepf, Felix Alexander. Quantitative interaction proteomics by affinity purification and mass spectrometry.

Degree: 2009, ETH Zürich

Subjects/Keywords: PROTEOM (PROTEINE UND PEPTIDE); PROTEIN-PROTEIN-WECHSELWIRKUNGEN; MASSENSPEKTROSKOPIE + MASSENSPEKTROMETRIE (BIOLOGISCHE TECHNIKEN); PROTEINE + POLYPEPTIDE (BIOCHEMIE); TRENN- UND REINIGUNGSVERFAHREN (BIOCHEMIE); PROTEOME (PROTEINS AND PEPTIDES); PROTEIN-PROTEIN INTERACTIONS; MASS SPECTROSCOPY + MASS SPECTROMETRY (BIOLOGICAL TECHNIQUES); PROTEINS + POLYPEPTIDES (BIOCHEMISTRY); SEPARATION TECHNIQUES + PURIFICATION TECHNIQUES (BIOCHEMISTRY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Wepf, F. A. (2009). Quantitative interaction proteomics by affinity purification and mass spectrometry. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/151634

Chicago Manual of Style (16th Edition):

Wepf, Felix Alexander. “Quantitative interaction proteomics by affinity purification and mass spectrometry.” 2009. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/151634.

MLA Handbook (7th Edition):

Wepf, Felix Alexander. “Quantitative interaction proteomics by affinity purification and mass spectrometry.” 2009. Web. 16 Jul 2019.

Vancouver:

Wepf FA. Quantitative interaction proteomics by affinity purification and mass spectrometry. [Internet] [Doctoral dissertation]. ETH Zürich; 2009. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/151634.

Council of Science Editors:

Wepf FA. Quantitative interaction proteomics by affinity purification and mass spectrometry. [Doctoral Dissertation]. ETH Zürich; 2009. Available from: http://hdl.handle.net/20.500.11850/151634


University of Florida

19. Lackner, Cari Aspacher, 1972-. Vaccinia virus transcript release requires the vaccinia virus protein A18 and a host cell factor.

Degree: 2000, University of Florida

Subjects/Keywords: DNA; Genes; In vitro fertilization; Nucleotides; Peptide elongation factors; Purification; RNA; Signals; Vaccinia; Vaccinia virus; Department of Molecular Genetics and Microbiology thesis Ph.D ( mesh ); Gene Expression Regulation ( mesh ); Research ( mesh ); Transcription, Genetic ( mesh ); Vaccinia virus  – genetics ( mesh ); Vaccinia virus  – physiology ( mesh ); Viral Proteins ( mesh )

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APA (6th Edition):

Lackner, Cari Aspacher, 1. (2000). Vaccinia virus transcript release requires the vaccinia virus protein A18 and a host cell factor. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00022099

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):

Lackner, Cari Aspacher, 1972-. “Vaccinia virus transcript release requires the vaccinia virus protein A18 and a host cell factor.” 2000. Thesis, University of Florida. Accessed July 16, 2019. http://ufdc.ufl.edu/AA00022099.

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

MLA Handbook (7th Edition):

Lackner, Cari Aspacher, 1972-. “Vaccinia virus transcript release requires the vaccinia virus protein A18 and a host cell factor.” 2000. Web. 16 Jul 2019.

Vancouver:

Lackner, Cari Aspacher 1. Vaccinia virus transcript release requires the vaccinia virus protein A18 and a host cell factor. [Internet] [Thesis]. University of Florida; 2000. [cited 2019 Jul 16]. Available from: http://ufdc.ufl.edu/AA00022099.

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

Council of Science Editors:

Lackner, Cari Aspacher 1. Vaccinia virus transcript release requires the vaccinia virus protein A18 and a host cell factor. [Thesis]. University of Florida; 2000. Available from: http://ufdc.ufl.edu/AA00022099

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


ETH Zürich

20. Pfister, David E. Processes for the Production of PEGylated Proteins.

Degree: 2015, ETH Zürich

Subjects/Keywords: PROTEINE, POLYPEPTIDE, ENZYME, ENZYMINHIBITOREN, PEPTIDE (PHARMAZIE); POLYETHYLENGLYKOLE (KUNSTSTOFFE); POLYMERE ARZNEIMITTELTRÄGER; KONJUGIERTE PROTEINE + PROTEIDE; ARZNEIMITTELREINIGUNG; IONENCHROMATOGRAPHIE + IONENAUSTAUSCHCHROMATOGRAPHIE + IONENPAARCHROMATOGRAPHIE; PROTEINS, POLYPEPTIDES, ENZYMES, ENZYME INHIBITORS, PEPTIDES (PHARMACY); POLYETHYLENE GLYCOLS (PLASTICS); POLYMERIC DRUG CARRIERS (GALENICS); CONJUGATED PROTEINS + PROTEIDS; PURIFICATION OF PHARMACEUTICAL DRUGS; ION CHROMATOGRAPHY + ION EXCHANGE CHROMATOGRAPHY + ION-PAIR PARTITION CHROMATOGRAPHY; info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/610; Life sciences; Medical sciences, medicine

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APA (6th Edition):

Pfister, D. E. (2015). Processes for the Production of PEGylated Proteins. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155327

Chicago Manual of Style (16th Edition):

Pfister, David E. “Processes for the Production of PEGylated Proteins.” 2015. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/155327.

MLA Handbook (7th Edition):

Pfister, David E. “Processes for the Production of PEGylated Proteins.” 2015. Web. 16 Jul 2019.

Vancouver:

Pfister DE. Processes for the Production of PEGylated Proteins. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/155327.

Council of Science Editors:

Pfister DE. Processes for the Production of PEGylated Proteins. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/155327


ETH Zürich

21. Vučkovič Müller, Živa. Development of a strategy for structural determination of α2C and β3 adrenergic receptors.

Degree: 2017, ETH Zürich

Subjects/Keywords: G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); ADRENERGE REZEPTOREN (NEUROLOGIE); ARZNEIMITTELREZEPTOREN (PHARMAKOLOGIE); ANALYSE VON STRUKTUR UND EIGENSCHAFTEN VON BIOMOLEKÜLEN; TRENN- UND REINIGUNGSVERFAHREN FÜR PROTEINE UND PEPTIDE; G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); ADRENERGIC RECEPTORS (NEUROLOGY); DRUG RECEPTORS (PHARMACOLOGY); ANALYSIS OF STRUCTURE AND PROPERTIES OF BIOMOLECULES; SEPARATION TECHNIQUES AND PURIFICATION TECHNIQUES FOR PROTEINS AND PEPTIDES; info:eu-repo/classification/ddc/570; Life sciences

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

APA (6th Edition):

Vučkovič Müller, . (2017). Development of a strategy for structural determination of α2C and β3 adrenergic receptors. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/156277

Chicago Manual of Style (16th Edition):

Vučkovič Müller, Živa. “Development of a strategy for structural determination of α2C and β3 adrenergic receptors.” 2017. Doctoral Dissertation, ETH Zürich. Accessed July 16, 2019. http://hdl.handle.net/20.500.11850/156277.

MLA Handbook (7th Edition):

Vučkovič Müller, Živa. “Development of a strategy for structural determination of α2C and β3 adrenergic receptors.” 2017. Web. 16 Jul 2019.

Vancouver:

Vučkovič Müller . Development of a strategy for structural determination of α2C and β3 adrenergic receptors. [Internet] [Doctoral dissertation]. ETH Zürich; 2017. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/20.500.11850/156277.

Council of Science Editors:

Vučkovič Müller . Development of a strategy for structural determination of α2C and β3 adrenergic receptors. [Doctoral Dissertation]. ETH Zürich; 2017. Available from: http://hdl.handle.net/20.500.11850/156277

.