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504 related items for PubMed ID: 18694833
1. pCold-GST vector: a novel cold-shock vector containing GST tag for soluble protein production. Hayashi K, Kojima C. Protein Expr Purif; 2008 Nov; 62(1):120-7. PubMed ID: 18694833 [Abstract] [Full Text] [Related]
2. Efficient protein production method for NMR using soluble protein tags with cold shock expression vector. Hayashi K, Kojima C. J Biomol NMR; 2010 Nov; 48(3):147-55. PubMed ID: 20844927 [Abstract] [Full Text] [Related]
3. An automated method for high-throughput protein purification applied to a comparison of His-tag and GST-tag affinity chromatography. Scheich C, Sievert V, Büssow K. BMC Biotechnol; 2003 Jul 28; 3():12. PubMed ID: 12885298 [Abstract] [Full Text] [Related]
4. Improving expression and solubility of rice proteins produced as fusion proteins in Escherichia coli. Tsunoda Y, Sakai N, Kikuchi K, Katoh S, Akagi K, Miura-Ohnuma J, Tashiro Y, Murata K, Shibuya N, Katoh E. Protein Expr Purif; 2005 Aug 28; 42(2):268-77. PubMed ID: 15914031 [Abstract] [Full Text] [Related]
5. 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 28; 152():92-106. PubMed ID: 30036588 [Abstract] [Full Text] [Related]
6. Cold-shock induced high-yield protein production in Escherichia coli. Qing G, Ma LC, Khorchid A, Swapna GV, Mal TK, Takayama MM, Xia B, Phadtare S, Ke H, Acton T, Montelione GT, Ikura M, Inouye M. Nat Biotechnol; 2004 Jul 28; 22(7):877-82. PubMed ID: 15195104 [Abstract] [Full Text] [Related]
7. Expression, purification of human vasostatin120-180 in Escherichia coli, and its anti-angiogenic characterization. Sun QM, Cao L, Fang L, Chen C, Dai J, Chen LL, Hua ZC. Protein Expr Purif; 2005 Feb 28; 39(2):288-95. PubMed ID: 15642481 [Abstract] [Full Text] [Related]
10. Overproduction of anti-Tn antibody MLS128 single-chain Fv fragment in Escherichia coli cytoplasm using a novel pCold-PDI vector. Subedi GP, Satoh T, Hanashima S, Ikeda A, Nakada H, Sato R, Mizuno M, Yuasa N, Fujita-Yamaguchi Y, Yamaguchi Y. Protein Expr Purif; 2012 Mar 28; 82(1):197-204. PubMed ID: 22245752 [Abstract] [Full Text] [Related]
11. Highly efficient protein expression and purification using bacterial hemoglobin fusion vector. Kwon SY, Choi YJ, Kang TH, Lee KH, Cha SS, Kim GH, Lee HS, Kim KT, Kim KJ. Plasmid; 2005 May 28; 53(3):274-82. PubMed ID: 15848232 [Abstract] [Full Text] [Related]
12. Dual expression system suitable for high-throughput fluorescence-based screening and production of soluble proteins. Braud S, Moutiez M, Belin P, Abello N, Drevet P, Zinn-Justin S, Courçon M, Masson C, Dassa J, Charbonnier JB, Boulain JC, Ménez A, Genet R, Gondry M. J Proteome Res; 2005 May 28; 4(6):2137-47. PubMed ID: 16335960 [Abstract] [Full Text] [Related]
13. A family of E. coli expression vectors for laboratory scale and high throughput soluble protein production. Cabrita LD, Dai W, Bottomley SP. BMC Biotechnol; 2006 Mar 01; 6():12. PubMed ID: 16509985 [Abstract] [Full Text] [Related]
14. Vectors for Cu(2+)-inducible production of glutathione S-transferase-fusion proteins for single-step purification from yeast. Ward AC, Castelli LA, Macreadie IG, Azad AA. Yeast; 1994 Apr 01; 10(4):441-9. PubMed ID: 7941730 [Abstract] [Full Text] [Related]
15. Preparation of soluble GST fusion proteins. Rebay I, Fehon RG. Cold Spring Harb Protoc; 2009 Nov 01; 2009(11):pdb.prot4996. PubMed ID: 20150052 [Abstract] [Full Text] [Related]
17. [Expression and characterization of soluble recombinant Ulp1p with glutathione S-transferase tag in Escherichia coli]. Fu J, Wang Q, Yin J, Liu M, Li N, Yao W, Ren G, Li L, Li D. Sheng Wu Gong Cheng Xue Bao; 2010 Jun 01; 26(6):837-42. PubMed ID: 20815266 [Abstract] [Full Text] [Related]
18. Glutathione S-transferase can be used as a C-terminal, enzymatically active dimerization module for a recombinant protease inhibitor, and functionally secreted into the periplasm of Escherichia coli. Tudyka T, Skerra A. Protein Sci; 1997 Oct 01; 6(10):2180-7. PubMed ID: 9336840 [Abstract] [Full Text] [Related]
19. Production of recombinant rat interleukin-6 in Escherichia coli using a novel highly efficient expression vector pGEX-3T. Frorath B, Abney CC, Berthold H, Scanarini M, Northemann W. Biotechniques; 1992 Apr 01; 12(4):558-63. PubMed ID: 1503758 [Abstract] [Full Text] [Related]
20. An alternative use of basic pGEX vectors for producing both N- and C-terminal fusion proteins for production and affinity purification of antibodies. Aatsinki JT, Rajaniemi HJ. Protein Expr Purif; 2005 Apr 01; 40(2):287-91. PubMed ID: 15766870 [Abstract] [Full Text] [Related] Page: [Next] [New Search]