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| 产品名称： | YEp356 |
|---|---|
| 商品货号： | TS147100 |
| Designations： | YEp356 |
| Depositors： | CJ Lusty |
| Biosafety Level： | 1 |
| Vector Information： | Size (kb): 8.0000000000000000 Vector: YEp356 (plasmid) Promoters: Promoter none Construction: YEp353 (ATCC 37725), pUC18 Marker(s):URA3,ampR Construct size (kb): 8.0 Features: insert detection: lacZ marker(s): ampR, URA3 promoter: none replicon: pMB1, 2 micron |
| Applications： | YE-type (episomal) shuttle vector promoter-cloning vector shuttle vector |
| Comments： | The cleavage position in the reading frame for cloning sites is (where 3 = between triplets): EcoRI-2; SacI-3; KpnI-3; SmaI-2; BamHI-2; XbaI-2; SalI-2; PstI-3; SphI-3; HindIII-2. The SacI site is not unique. Cloning into the EcoRI, SacI, KpnI SmaI, BamHI, or XbaI sites leads to a TAG stop codon within the downstream XbaI site of the multiple cloning region. Restriction digests of the clone give the following sizes (kb): PstI--8.0; HindIII--8.0; SalI--8.0; EcoRI--8.0; BamHI--8.0. One of 3 promoter-cloning, YE type shuttle vectors (TS147100 - 37733) with URA3 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: 5GA ATT CGA GCT CGG TAC CCG GGG ATC CTC TAG AGT CGA CCT GCA GGC ATG CAA GCT TGC GAT CCC 3, 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 |