These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
192 related articles for article (PubMed ID: 8200533)
1. Direct cloning of unmodified PCR products by exploiting an engineered restriction site. Testori A; Listowsky I; Sollitti P Gene; 1994 May; 143(1):151-2. PubMed ID: 8200533 [TBL] [Abstract][Full Text] [Related]
2. Cloning unmodified PCR products using engineered XcmI restriction sites in a portable cassette. Testori A; Sollitti P Methods Mol Biol; 1997; 67():89-100. PubMed ID: 9031134 [No Abstract] [Full Text] [Related]
3. XcmI site-containing vector for direct cloning and in vitro transcription of PCR product. Arashi-Heese N; Miwa M; Shibata H Mol Biotechnol; 1999 Oct; 12(3):281-3. PubMed ID: 10631685 [TBL] [Abstract][Full Text] [Related]
4. pUCPCR1. A vector for direct cloning of PCR products in a double Xcm1 restriction site offering compatible single 3'-overhanging T residues. de Vries E Mol Biotechnol; 1998 Dec; 10(3):273-4. PubMed ID: 9951708 [TBL] [Abstract][Full Text] [Related]
6. Bifunctional lacZ alpha-ccdB genes for selective cloning of PCR products. Gabant P; Drèze PL; Van Reeth T; Szpirer J; Szpirer C Biotechniques; 1997 Nov; 23(5):938-41. PubMed ID: 9383562 [TBL] [Abstract][Full Text] [Related]
7. Construction of an XcmI-generated T vector bearing green fluorescent protein marker for direct cloning of PCR products. Park HK; Zeng C Anal Biochem; 2007 Jan; 360(1):144-5. PubMed ID: 17113027 [No Abstract] [Full Text] [Related]
8. Construction of T-tailed vectors derived from a pUC plasmid: a rapid system for direct cloning of unmodified PCR products. Ido E; Hayami M Biosci Biotechnol Biochem; 1997 Oct; 61(10):1766-7. PubMed ID: 9362125 [TBL] [Abstract][Full Text] [Related]
9. A simple method to construct T-vectors using XcmI cassettes amplified by nonspecific PCR. Jo C; Jo SA Plasmid; 2001 Jan; 45(1):37-40. PubMed ID: 11319930 [TBL] [Abstract][Full Text] [Related]
12. pSDTV vector: a modification of the pBluescript SK+ plasmid in order to perform PCR-fragments TA-cloning using Eam1105I restriction endonuclease. Dimov SG Mol Biol Rep; 2012 May; 39(5):6133-9. PubMed ID: 22203488 [TBL] [Abstract][Full Text] [Related]
13. Ligation-independent cloning of PCR products (LIC-PCR). Aslanidis C; de Jong PJ Nucleic Acids Res; 1990 Oct; 18(20):6069-74. PubMed ID: 2235490 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Construction of new T vectors for direct cloning of PCR products. Ichihara Y; Kurosawa Y Gene; 1993 Aug; 130(1):153-4. PubMed ID: 8344524 [TBL] [Abstract][Full Text] [Related]
17. Directional cloning of native PCR products with preformed sticky ends (autosticky PCR). Gál J; Schnell R; Szekeres S; Kálmán M Mol Gen Genet; 1999 Jan; 260(6):569-73. PubMed ID: 9928936 [TBL] [Abstract][Full Text] [Related]
18. Minimal length requirement of the single-stranded tails for ligation-independent cloning (LIC) of PCR products. Aslanidis C; de Jong PJ; Schmitz G PCR Methods Appl; 1994 Dec; 4(3):172-7. PubMed ID: 7580902 [TBL] [Abstract][Full Text] [Related]
19. New vectors for direct cloning of PCR products. Cha J; Bishai W; Chandrasegaran S Gene; 1993 Dec; 136(1-2):369-70. PubMed ID: 8294034 [TBL] [Abstract][Full Text] [Related]