BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

488 related articles for article (PubMed ID: 21125392)

  • 1. Enhancing the solubility of recombinant proteins in Escherichia coli by using hexahistidine-tagged maltose-binding protein as a fusion partner.
    Sun P; Tropea JE; Waugh DS
    Methods Mol Biol; 2011; 705():259-74. PubMed ID: 21125392
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hexahistidine-tagged maltose-binding protein as a fusion partner for the production of soluble recombinant proteins in Escherichia coli.
    Austin BP; Nallamsetty S; Waugh DS
    Methods Mol Biol; 2009; 498():157-72. PubMed ID: 18988025
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expression and Purification of Recombinant Proteins in Escherichia coli with a His
    Raran-Kurussi S; Waugh DS
    Methods Mol Biol; 2017; 1607():1-15. PubMed ID: 28573567
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-level expression of soluble recombinant proteins in Escherichia coli using an HE-maltotriose-binding protein fusion tag.
    Han Y; Guo W; Su B; Guo Y; Wang J; Chu B; Yang G
    Protein Expr Purif; 2018 Feb; 142():25-31. PubMed ID: 28963004
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A generic method for the production of recombinant proteins in Escherichia coli using a dual hexahistidine-maltose-binding protein affinity tag.
    Tropea JE; Cherry S; Nallamsetty S; Bignon C; Waugh DS
    Methods Mol Biol; 2007; 363():1-19. PubMed ID: 17272834
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Systematic analysis of the expression, solubility and purification of a passenger protein in fusion with different tags.
    Bernier SC; Cantin L; Salesse C
    Protein Expr Purif; 2018 Dec; 152():92-106. PubMed ID: 30036588
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gateway vectors for the production of combinatorially-tagged His6-MBP fusion proteins in the cytoplasm and periplasm of Escherichia coli.
    Nallamsetty S; Austin BP; Penrose KJ; Waugh DS
    Protein Sci; 2005 Dec; 14(12):2964-71. PubMed ID: 16322578
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The ability to enhance the solubility of its fusion partners is an intrinsic property of maltose-binding protein but their folding is either spontaneous or chaperone-mediated.
    Raran-Kurussi S; Waugh DS
    PLoS One; 2012; 7(11):e49589. PubMed ID: 23166722
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expression and purification of soluble His(6)-tagged TEV protease.
    Tropea JE; Cherry S; Waugh DS
    Methods Mol Biol; 2009; 498():297-307. PubMed ID: 18988033
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Purification of Proteins Fused to Maltose-Binding Protein.
    Lebendiker M; Danieli T
    Methods Mol Biol; 2017; 1485():257-273. PubMed ID: 27730557
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Positional effects of fusion partners on the yield and solubility of MBP fusion proteins.
    Raran-Kurussi S; Keefe K; Waugh DS
    Protein Expr Purif; 2015 Jun; 110():159-64. PubMed ID: 25782741
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High yield purification of nanobodies from the periplasm of E. coli as fusions with the maltose binding protein.
    Salema V; Fernández LÁ
    Protein Expr Purif; 2013 Sep; 91(1):42-8. PubMed ID: 23856605
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Affinity Purification of a Recombinant Protein Expressed as a Fusion with the Maltose-Binding Protein (MBP) Tag.
    Duong-Ly KC; Gabelli SB
    Methods Enzymol; 2015; 559():17-26. PubMed ID: 26096500
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Purification of proteins fused to maltose-binding protein.
    Lebendiker M; Danieli T
    Methods Mol Biol; 2011; 681():281-93. PubMed ID: 20978971
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A comparison between MBP- and NT* as N-terminal fusion partner for recombinant protein production in E. coli.
    Raran-Kurussi S; Sharwanlal SB; Balasubramanian D; Mote KR
    Protein Expr Purif; 2022 Jan; 189():105991. PubMed ID: 34628000
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Single amino acid substitutions on the surface of Escherichia coli maltose-binding protein can have a profound impact on the solubility of fusion proteins.
    Fox JD; Kapust RB; Waugh DS
    Protein Sci; 2001 Mar; 10(3):622-30. PubMed ID: 11344330
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High level soluble production of functional ribonuclease inhibitor in Escherichia coli by fusing it to soluble partners.
    Guo W; Cao L; Jia Z; Wu G; Li T; Lu F; Lu Z
    Protein Expr Purif; 2011 Jun; 77(2):185-92. PubMed ID: 21292012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cu/Zn incorporation during purification of soluble human EC-SOD from E. coli stabilizes proper disulfide bond formation.
    Bae JY; Koo BK; Ryu HB; Song JA; Nguyen MT; Vu TT; Son YJ; Lee HK; Choe H
    Appl Biochem Biotechnol; 2013 Mar; 169(5):1633-47. PubMed ID: 23329142
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High-level expression of soluble protein in Escherichia coli using a His6-tag and maltose-binding-protein double-affinity fusion system.
    Pryor KD; Leiting B
    Protein Expr Purif; 1997 Aug; 10(3):309-19. PubMed ID: 9268677
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rescuing aggregation-prone proteins in Escherichia coli with a dual His₆-MBP tag.
    Needle D; Waugh DS
    Methods Mol Biol; 2014; 1177():81-94. PubMed ID: 24943316
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.