YIp366R (ATCC® 37758)

Applications: YI-type (integrating) shuttle vectorpromoter-cloning vectorshuttle vector  /  Depositors: CJ Lusty

Permits and Restrictions

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Designations YIp366R
Depositors CJ Lusty
Biosafety Level 1
Vector Information
Size (kb): 7.0000000000000000
Vector: YIp366R (plasmid)
Promoters: Promoter none
Construction: YEp366R (ATCC 37740), YIp351
Marker(s):LEU2,ampR
Construct size (kb): 7.0
Features: insert detection: lacZ
marker(s): ampR, LEU2
promoter: none
replicon: pMB1
Applications
YI-type (integrating) shuttle vector
promoter-cloning vector
shuttle vector
Comments
The cleavage position in the reading frame for cloning sites is (where 3 = between triplets): HindIII-1; SphI-2; PstI-2; SalI-1; XbaI-1; BamHI-1; SmaI-2; KpnI-2; SacI-2; EcoRI-1. The EcoRI, KpnI, and SacI sites are not unique.
Restriction digests of the clone give the following sizes (kb): HindIII-7.8; BamHI-7.8; PstI-7.8.
One of 3 promoter-cloning, YI type shuttle vectors (ATCC 37758 - 37760) with LEU2 selection in Saccharomyces cerevisiae, a beta-galactosidase reporter gene and multiple cloning sites differing in reading frame.
The sequence and reading frame of the multiple cloning sequence is: 5'AAG CTT GCA TGC CTG CAG GTC GAC TCT AGA GGA TCC CCG GGT ACC GAG CTC GAA TTC CCA GCT TGC GAT CCC3', from nucleotide 1 of the MCS through CCC for amino acid 8 of beta-galactosidase.
Media Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Growth Conditions
Temperature: 37.0°C
References

Myers AM, et al. Yeast shuttle and integrative vectors with multiple cloning sites suitable for construction of lacZ fusions. Gene 45: 299-310, 1986. PubMed: 3026915

Shipped freeze-dried
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