loxP-directed cloning: Use of Cre recombinase as a universal restriction enzyme

BioTechniques

Volumn 31, Issue 4, 2001, Pages 906-918

  Buchholz, F ^a   Bishop, M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIA; CHROMOSOMES; CLONING; ENZYMES;

CIRCULAR EPISOMES;

DNA;

CRE RECOMBINASE; DNA; DNA FRAGMENT; GENE PRODUCT; LOXP PROTEIN; RESTRICTION ENDONUCLEASE; UNCLASSIFIED DRUG;

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CLONING VECTOR; CONTROLLED STUDY; EPISOME; GENETIC MANIPULATION; HELA CELL; HUMAN; HUMAN CELL; IN VITRO STUDY; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PRACTICE GUIDELINE; RESTRICTION SITE;

EID: 0034788268     PISSN: 07366205     EISSN: None     Source Type: Journal    
DOI: 10.2144/01314rr02     Document Type: Article

References (18)

1. Simplified generation of targeting constructs using ET recombination
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5. Different thermostabilities of FLP and Cre recombinases: Implications for applied site-specific recombination
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14. Human apolipoprotein B transgenic mice generated with 207- and 145-kilo-base pair bacterial artificial chromosomes. Evidence that a distant 5′-element confers appropriate transgene expression in the intestine
15. Hormone-dependent translocation of vitamin D receptors is linked to transactivation
16. BAC-mediated gene-dosage analysis reveals a role for Ziprol (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin
17. A new logic for DNA engineering using recombination in Escherichia coli
18. Hormone-induced translocation of thyroid hormone receptors in living cells visualized using a receptor green fluorescent protein chimera