S. cerevisiae genomic library (ATCC® 87311)

Organism: Saccharomyces cerevisiae Meyen ex E.C. Hansen  /  Clone Type: Library  /  Depositors: SJ Elledge

Permits and Restrictions

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Designations S. cerevisiae genomic library
Species Saccharomyces cerevisiae Meyen ex E.C. Hansen
Depositors SJ Elledge
Applications
To convert bacteriophage lambda clones to plasmid via the cre-lox recombination system, use of BNN132 (ATCC 47059) is recommended.
Vector
DESCRIPTION OF VECTOR COMPONENT:
Name of vector: lambdaYES-R
Intact vector size: 42.600
Type of vector: phage
Vector end: XhoI
Vector end: XhoI
Cloning sites: XhoI, EcoRI
Polylinker sites: EcoRI XhoI EcoRI
Construction: lambdagt6; pSE936
Host range: Escherichia coli
Features (with orientation and position when available):
other: left arm (19.6 kb), ->
other: lox, ->
replicon: ARS1
replicon: pMB1
marker(s): ampR, <-
promoter for expression: GAL1, ->
MCS: XhoI EcoRI, ->
promoter for expression: lac, <-
transcription terminator: HIS3, ->
marker(s): URA3, ->
centromere: CEN4
other: lox, ->
other: right arm (15.2 kb, with cI857)
Cross references:
Vector
DNA: genomic
Insert size range: 4 - 7 kb
Media ATCC® Medium 1592: SM buffer
Biosafety Level 1
Shipping Information Distributed: frozen bacteria-free lysate (volume: 0.4 mL)
Comments
To convert bacteriophage lambda clones to plasmid via the cre-lox recombination system, use of BNN132 (ATCC 47059) is recommended.
Classification Saccharomycetes, Saccharomycetidae, Saccharomycetales, Saccharomycetaceae, Saccharomycetaceae, Saccharomyces, cerevisiae
References

Elledge SJ, et al. lambdaYES: a multifunctional cDNA expression vector for the isolation of genes by complementation of yeast and Escherichia coli mutations. Proc. Natl. Acad. Sci. USA 88: 1731-1735, 1991. PubMed: 1848010

Ramer SW, et al. Dominant genetics using a yeast genomic library under the control of a strong inducible promoter. Proc. Natl. Acad. Sci. USA 89: 11589-11593, 1992. PubMed: 1454852

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