Development of new T-vectors containing the luciferase gene: Easy application for direct cloning of a promoter DNA

Applied Biochemistry and Biotechnology - Part B Molecular Biotechnology

Volumn 19, Issue 3, 2001, Pages 331-334

  Jo, C ^a   Kang, B ^a   Jo, S A ^a  

^a Korea National Institute of Health   (South Korea)

Author keywords

Luciferase gene, polymerase chain reaction; Promoter analysis, XcmI cassette; T vector

Indexed keywords

CHOLINERGIC RECEPTOR; LUCIFERASE; NEU DIFFERENTIATION FACTOR; RECEPTOR SUBUNIT;

ANIMAL CELL; CONTROLLED STUDY; DNA SEQUENCE; DNA VECTOR; GENE AMPLIFICATION; GENE CASSETTE; GENE CONSTRUCT; GENE MUTATION; HUMAN; HUMAN CELL; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PLASMID; POLYMERASE CHAIN REACTION; PROMOTER REGION; RESTRICTION SITE; REVIEW;

BASE SEQUENCE; DNA PRIMERS; GENETIC VECTORS; LUCIFERASES; POLYMERASE CHAIN REACTION;

ANIMALIA; MURINAE;

EID: 0035159764     PISSN: 10736085     EISSN: None     Source Type: Journal    
DOI: 10.1385/MB:19:3:331     Document Type: Review

References (12)

1. Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases
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4. PUCPCR1. A vector for direct cloning of PCR products in a double XcmI restriction site offering compatible single 3′-overhang T residues
5. XcmI-containing vector for direct cloning of PCR products
6. New vectors for direct cloning of PCR products
7. Direct cloning of polymerase chain reaction products in an XcmI T-vector
8. General method for direct cloning of DNA fragments generated by the polymerase chain reaction
9. A universal method for the direct cloning of PCR amplified nucleic acid
10. Construction of new T vectors for direct cloning of PCR products
11. A simple method to construct T-vectors using XcmI cassettes amplified by nonspecific PCR
12. Neuregulins are concentrated at nerve-muscle synapses and activate ACh-receptor gene expression