产品名称: | YIp366R |
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商品货号: | TS138491 |
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 (TS138491 - 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: 5AAG 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: | ATCC® 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 |