96 related articles for article (PubMed ID: 7642128)
1. Introduction of the octanucleotide restriction site SwaI into the bicistronic vector pTiSDT for high level synthesis of proteins.
Grütz G; Randow F; Niemann B; von Baehr R
Gene; 1995 Aug; 161(1):135-6. PubMed ID: 7642128
[TBL] [Abstract][Full Text] [Related]
2. XcmI-containing vector for direct cloning of PCR products.
Borovkov AY; Rivkin MI
Biotechniques; 1997 May; 22(5):812-4. PubMed ID: 9149852
[No Abstract] [Full Text] [Related]
3. A unique type II restriction endonuclease FspAI, that recognizes the octanucleotide sequence 5'-RTGC/GCAY-3'.
Kesminiene A; Maneliene Z; Vitkute J; Petrusyte M; Janulaitis A
Nucleic Acids Res; 2001 Dec; 29(24):E120. PubMed ID: 11812857
[TBL] [Abstract][Full Text] [Related]
4. Mapping domains in proteins: dissection and expression of Escherichia coli adenylyl cyclase.
Reddy P; Hoskins J; McKenney K
Anal Biochem; 1995 Nov; 231(2):282-6. PubMed ID: 8594974
[TBL] [Abstract][Full Text] [Related]
5. SwaI, a unique restriction endonuclease from Staphylococcus warneri, which recognizes 5'-ATTTAAAT-3'.
Lechner M; Frey B; Laue F; Anton-Botella J; Smith CL; Ankenbauer W; Schmitz GG
Nucleic Acids Res; 1992 May; 20(9):2293-6. PubMed ID: 1594448
[TBL] [Abstract][Full Text] [Related]
6. Hyperexpression and purification of Escherichia coli adenylate cyclase using a vector designed for expression of lethal gene products.
Reddy P; Peterkofsky A; McKenney K
Nucleic Acids Res; 1989 Dec; 17(24):10473-88. PubMed ID: 2557591
[TBL] [Abstract][Full Text] [Related]
7. Construction of a directional T vector for cloning PCR products and expression in Escherichia coli.
Liang XY; Liang ZC; Zhang Z; Zhou JJ; Liu SY; Tian SL
Plasmid; 2015 May; 79():15-21. PubMed ID: 25681561
[TBL] [Abstract][Full Text] [Related]
8. Cloning, sequencing and expression of the Taq I restriction-modification system.
Slatko BE; Benner JS; Jager-Quinton T; Moran LS; Simcox TG; Van Cott EM; Wilson GG
Nucleic Acids Res; 1987 Dec; 15(23):9781-96. PubMed ID: 2827113
[TBL] [Abstract][Full Text] [Related]
9. An efficient method for blunt-end ligation of PCR products.
Liu ZG; Schwartz LM
Biotechniques; 1992 Jan; 12(1):28, 30. PubMed ID: 1734919
[TBL] [Abstract][Full Text] [Related]
10. Oligonucleotide-directed site-specific integration of high complexity libraries into ssDNA templates.
Hale MB; Nolan GP; Wolkowicz R
Nucleic Acids Res; 2004 Jan; 32(2):e22. PubMed ID: 14752044
[TBL] [Abstract][Full Text] [Related]
11. TGATG vector: a new expression system for cloned foreign genes in Escherichia coli cells.
Mashko SV; Veiko VP; Lapidus AL; Lebedeva MI; Mochulsky AV; Shechter II; Trukhan ME; Ratmanova KI; Rebentish BA; Kaluzhsky VE
Gene; 1990 Mar; 88(1):121-6. PubMed ID: 2187746
[TBL] [Abstract][Full Text] [Related]
12. New high-cloning-efficiency vectors for complementation studies and recombinant protein overproduction in Escherichia coli and Salmonella enterica.
VanDrisse CM; Escalante-Semerena JC
Plasmid; 2016 Jul; 86():1-6. PubMed ID: 27234933
[TBL] [Abstract][Full Text] [Related]
13. SrfI, a new type-II restriction endonuclease that recognizes the octanucleotide sequence, [sequence: see text].
Simcox TG; Marsh SJ; Gross EA; Lernhardt W; Davis S; Simcox ME
Gene; 1991 Dec; 109(1):121-3. PubMed ID: 1756971
[TBL] [Abstract][Full Text] [Related]
14. [Plasmid vectors pBBV for the cloning and regeneration of DNA fragments with any terminal nucleotide sequence].
Dobrynin VN; Krobko VG; Shingarova LN; Bystrov NS; Filippov SA
Dokl Akad Nauk SSSR; 1984; 278(4):1002-5. PubMed ID: 6097428
[No Abstract] [Full Text] [Related]
15. Modified bacteriophage lambda promoter vectors for overproduction of proteins in Escherichia coli.
Elvin CM; Thompson PR; Argall ME; Hendry P; Stamford NP; Lilley PE; Dixon NE
Gene; 1990 Mar; 87(1):123-6. PubMed ID: 2139621
[TBL] [Abstract][Full Text] [Related]
16. DNA cleavage by restriction endonuclease PflMI is inhibited in recognition sites modified by dcm methylation.
Sturm RA; Yaciuk P
Nucleic Acids Res; 1989 May; 17(9):3615. PubMed ID: 2657665
[No Abstract] [Full Text] [Related]
17. A rapid and versatile method to transfer an insert between single-stranded vectors and reverse its orientation.
Adey NB; Hutchison CA
Nucleic Acids Res; 1991 Jun; 19(12):3461-2. PubMed ID: 2062665
[No Abstract] [Full Text] [Related]
18. 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
[TBL] [Abstract][Full Text] [Related]
19. Molecular cloning and expression of NlaIII restriction-modification system in E. coli.
Morgan RD; Camp RR; Wilson GG; Xu SY
Gene; 1996 Dec; 183(1-2):215-8. PubMed ID: 8996109
[TBL] [Abstract][Full Text] [Related]
20. Reduced chloramphenicol acetyltransferase activity observed with vectors containing an upstream SphI recognition sequence.
Alam J; Yu N; Irias S; Cook JL; Vig E
Biotechniques; 1991 Apr; 10(4):422, 424-5. PubMed ID: 1867848
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]