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Strains and vectors on this page are available by
contacting info@twohybridservice.org
VectorsThe sequence files available here were assembled and annotated based on published plasmids and sequences available in Genbank. The .gb files are text files in the Genbank format. The pdf contains annotated sequences and the jpg is a map. In most cases a VectorNTI file is also available upon request. The size of each file is in parentheses following the file name.Bait Vectors - LexA DNA-binding domainpNLex [also known as pNLex(NLS)]HIS3 2µ ADH1p LexA NLS. Derived from pLexA(202+PL). Contains an SV40 nuclear localization signal (NLS) coding sequence downstream of LexA and upstream of the mcs. pNLexAattRHIS3 2µ ADH1p LexA NLS attR. Destination version of pNLex for use with the GatewayTM (Invitrogen) in vitro cloning system. Finley et al., 2002, Gene 285, 49-57. pEG202HIS3 2µ ADH1p LexA mcs. The most common plasmid used in the LexA two-hybrid system. Similar to pLexA(202+PL) but with a better multiple cloning site downstream of LexA. The sequence file was derived from the version marketed by Clontech and from Genbank Accession Number U89960. Estojak et al., 1995, Mol. Cell. Biol. 15, 5820-5829. pHZ5HIS3 2µ MAL62p LexA NLS. HIS3 2µ yeast
vector for regulated expression of N-terminal LexA
fusions using the MAL62 promoter. Includes at the
C-terminal end of LexA. This is the BD vector currently
used by the Finley lab for most yeast two-hybrid
studies. Finley et al., 2002, Gene 285, 49-57. pHZ5attRHIS3 2µ MAL62p LexA NLS attR. Destination
vector version of pHZ5 for use with the GatewayTM
(Invitrogen) in vitro cloning system. Finley et al.,
2002, Gene 285, 49-57. pLexA(202+PL)HIS3 2µ ADH1p LexA. This is the granddaddy of
all LexA expression vectors. HIS3 2µ with the
ADH1 promoter driving expression of LexA. Most
(possibly all) of the other LexA vectors shown here were
derived from this common ancestor. Ruden et al., 1991,
Nature 350, 250-252. Activation Domain VectorspJZ4TRP1 2µ GAL1p NLS-B42AD-HAtag mcs CYC1t. For regulated expression of AD fusions
from the GAL1 promoter. Similar to pJG4-5 except with an
F1 origin and the CYC1 terminator instead of ADH1t to reduce possible recombination with the
BD vector. This is the AD vector currently used by the
Finley lab for most yeast two-hybrid studies. pJG4-5TRP1 2µ GAL1p NLS-B42AD-HAtag mcs
ADH1t. This is the original AD vector for the Brent
lab LexA two-hybrid system. The sequence file was
derived from the version marketed by Clontech and from
Genbank Accession Number U89961. Gyuris et al., 1993,
Cell 75, 791-803. |
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