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646 related items for PubMed ID: 17447725
1. Expression vectors for enzyme restriction- and ligation-independent cloning for producing recombinant His-fusion proteins. de las Rivas B, Curiel JA, Mancheño JM, Muñoz R. Biotechnol Prog; 2007; 23(3):680-6. PubMed ID: 17447725 [Abstract] [Full Text] [Related]
2. The pURI family of expression vectors: a versatile set of ligation independent cloning plasmids for producing recombinant His-fusion proteins. Curiel JA, de Las Rivas B, Mancheño JM, Muñoz R. Protein Expr Purif; 2011 Mar; 76(1):44-53. PubMed ID: 21055470 [Abstract] [Full Text] [Related]
3. An Escherichia coli expression vector that allows recovery of proteins with native N-termini from purified calmodulin-binding peptide fusions. Wyborski DL, Bauer JC, Zheng CF, Felts K, Vaillancourt P. Protein Expr Purif; 1999 Jun; 16(1):1-10. PubMed ID: 10336854 [Abstract] [Full Text] [Related]
4. A set of ligation-independent expression vectors for co-expression of proteins in Escherichia coli. Chanda PK, Edris WA, Kennedy JD. Protein Expr Purif; 2006 May; 47(1):217-24. PubMed ID: 16325426 [Abstract] [Full Text] [Related]
8. 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; 53(3):274-82. PubMed ID: 15848232 [Abstract] [Full Text] [Related]
9. Highly efficient eukaryotic gene expression vectors for peptide secretion. Chu TH, Martinez I, Olson P, Dornburg R. Biotechniques; 1995 May; 18(5):890-6, 898-9. PubMed ID: 7619496 [Abstract] [Full Text] [Related]
10. A new vector for high-throughput, ligation-independent cloning encoding a tobacco etch virus protease cleavage site. Stols L, Gu M, Dieckman L, Raffen R, Collart FR, Donnelly MI. Protein Expr Purif; 2002 Jun; 25(1):8-15. PubMed ID: 12071693 [Abstract] [Full Text] [Related]
15. A modular set of prokaryotic and eukaryotic expression vectors. Melcher K. Anal Biochem; 2000 Jan 01; 277(1):109-20. PubMed ID: 10610695 [Abstract] [Full Text] [Related]
16. pAM401-based shuttle vectors that enable overexpression of promoterless genes and one-step purification of tag fusion proteins directly from Enterococcus faecalis. Fujimoto S, Ike Y. Appl Environ Microbiol; 2001 Mar 01; 67(3):1262-7. PubMed ID: 11229919 [Abstract] [Full Text] [Related]
17. Preparation of recombinant thioredoxin fused N-terminal proCNP: Analysis of enterokinase cleavage products reveals new enterokinase cleavage sites. Liew OW, Ching Chong JP, Yandle TG, Brennan SO. Protein Expr Purif; 2005 Jun 01; 41(2):332-40. PubMed ID: 15866719 [Abstract] [Full Text] [Related]