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Volumn 48, Issue 2, 2002, Pages 160-163

Construction of two pGEM-7Zf(+) phagemid T-tail vectors using AhdI-restriction endonuclease sites for direct cloning of PCR products

Author keywords

[No Author keywords available]

Indexed keywords

BETA GALACTOSIDASE; BETA LACTAMASE; PLASMID VECTOR; RESTRICTION ENDONUCLEASE; RNA POLYMERASE;

EID: 0036425804     PISSN: 0147619X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0147-619X(02)00122-1     Document Type: Article
Times cited : (16)

References (16)
  • 1
    • 0033426926 scopus 로고    scopus 로고
    • XcmI site-containing vector for direct cloning and in vitro transcription of PCR product
    • Arashi, N., Miwa, M., Shibata, H., 1999. XcmI site-containing vector for direct cloning and in vitro transcription of PCR product. Mol. Biotechnol. 12, 281-283.
    • (1999) Mol. Biotechnol. , vol.12 , pp. 281-283
    • Arashi, N.1    Miwa, M.2    Shibata, H.3
  • 2
    • 0030996054 scopus 로고    scopus 로고
    • XcmI-containing vector for direct cloning of PCR products
    • Borovkov, A.Y., Rivkin, M.I., 1997. XcmI-containing vector for direct cloning of PCR products. BioTechniques 22, 812-814.
    • (1997) BioTechniques , vol.22 , pp. 812-814
    • Borovkov, A.Y.1    Rivkin, M.I.2
  • 3
    • 0027731373 scopus 로고
    • New vectors for direct cloning of PCR products
    • Cha, J., Bishai, W., Chandrasegaran, S., 1993. New vectors for direct cloning of PCR products. Gene 136, 369-370.
    • (1993) Gene , vol.136 , pp. 369-370
    • Cha, J.1    Bishai, W.2    Chandrasegaran, S.3
  • 4
    • 0023734473 scopus 로고    scopus 로고
    • Novel non-templated nucleotide addition reactions catalyzed prokaryotic and eucaryotic DNA polymerase
    • Clark, J.M., 1998. Novel non-templated nucleotide addition reactions catalyzed prokaryotic and eucaryotic DNA polymerase. Nucleic Acids Res. 16, 9677-9686.
    • (1998) Nucleic Acids Res. , vol.16 , pp. 9677-9686
    • Clark, J.M.1
  • 5
    • 0032449305 scopus 로고    scopus 로고
    • pUCPCR1. A vector for direct cloning of PCR products in a double XcmI restriction site offering compatible single 3′-overhanging T residues
    • De Vries, E., 1998. pUCPCR1. A vector for direct cloning of PCR products in a double XcmI restriction site offering compatible single 3′-overhanging T residues. Mol. Biotechnol. 10, 273-274.
    • (1998) Mol. Biotechnol. , vol.10 , pp. 273-274
    • De Vries, E.1
  • 6
    • 0026067071 scopus 로고
    • A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors
    • Holton, T.A., Graham, M.W., 1991. A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors. Nucleic Acids Res. 19, 1156.
    • (1991) Nucleic Acids Res. , vol.19 , pp. 1156
    • Holton, T.A.1    Graham, M.W.2
  • 7
    • 0027228253 scopus 로고
    • Construction of new T vectors for direct cloning of PCR products
    • Ichihara, Y., Kurosawa, Y., 1993. Construction of new T vectors for direct cloning of PCR products. Gene 130, 153-154.
    • (1993) Gene , vol.130 , pp. 153-154
    • Ichihara, Y.1    Kurosawa, Y.2
  • 8
    • 0035122606 scopus 로고    scopus 로고
    • A simple method to construct T vectors using XcmI cassettes amplified by nonspecific PCR
    • Jo, C., Jo, S., 2001. A simple method to construct T vectors using XcmI cassettes amplified by nonspecific PCR. Plasmid 45, 37-40.
    • (2001) Plasmid , vol.45 , pp. 37-40
    • Jo, C.1    Jo, S.2
  • 9
    • 0025776435 scopus 로고
    • General method for direct cloning of DNA fragments generated by polymerase chain reaction
    • Kovalic, D., Kwak, J., Weisblum, B., 1991. General method for direct cloning of DNA fragments generated by polymerase chain reaction. Nucleic Acids Res. 19, 4560.
    • (1991) Nucleic Acids Res. , vol.19 , pp. 4560
    • Kovalic, D.1    Kwak, J.2    Weisblum, B.3
  • 12
    • 0025321244 scopus 로고
    • PCR-induced (ligase-free) subcloning: A rapid reliable method to subclone polymerase chain reaction (PCR) products
    • Schuldiner, A.R., Scott, L.A., Roth, J., 1990. PCR-induced (ligase-free) subcloning: A rapid reliable method to subclone polymerase chain reaction (PCR) products. Nucleic Acids Res. 18, 1920.
    • (1990) Nucleic Acids Res. , vol.18 , pp. 1920
    • Schuldiner, A.R.1    Scott, L.A.2    Roth, J.3
  • 13
    • 0027453539 scopus 로고
    • XcmI as a universal restriction enzyme for single-stranded DNA
    • Shaw, P., Mok, Y., 1993. XcmI as a universal restriction enzyme for single-stranded DNA. Gene 133, 85-89.
    • (1993) Gene , vol.133 , pp. 85-89
    • Shaw, P.1    Mok, Y.2
  • 14
    • 0031023680 scopus 로고    scopus 로고
    • Optimized conditions for cloning PCR products into an XcmI T vector
    • Schutte, B.C., Ranade, K., Pruessner, J., Dracopoli, N., 1997. Optimized conditions for cloning PCR products into an XcmI T vector. BioTechniques 22, 40-44.
    • (1997) BioTechniques , vol.22 , pp. 40-44
    • Schutte, B.C.1    Ranade, K.2    Pruessner, J.3    Dracopoli, N.4
  • 15
    • 0028605713 scopus 로고
    • Novel approach to molecular cloning and polynucleotide synthesis using vaccinia DNA topoisomerase
    • Shuman, S., 1994. Novel approach to molecular cloning and polynucleotide synthesis using vaccinia DNA topoisomerase. J. Biol. Chem. 265 (51), 32678-32684.
    • (1994) J. Biol. Chem. , vol.265 , Issue.51 , pp. 32678-32684
    • Shuman, S.1
  • 16
    • 0027229638 scopus 로고
    • Efficient cloning of the polymerase chain reaction directly into the single stranded bacteriophage M13mp18
    • Zimmer, W., 1993. Efficient cloning of the polymerase chain reaction directly into the single stranded bacteriophage M13mp18. Nucleic Acids Res. 21, 773-774.
    • (1993) Nucleic Acids Res. , vol.21 , pp. 773-774
    • Zimmer, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.