| 产品名称: | pMLB1034 plasmid in E. coli |
|---|---|
| 商品货号: | TS164048 |
| Designations: | pMLB1034 plasmid in E. coli |
| Depositors: | ML Berman |
| Biosafety Level: | 1 |
| Vector Information: | Size (kb): 6.26 Vector: pMLB1034 (plasmid) Promoters: Promoter none Construction: pMC871, pBR322 Marker(s):ampR Construct size (kb): 6.26 Features: insert detection: lacZ marker(s): ampR promoter: none replicon: pMB1 |
| Applications: | promoter-cloning vector vector permitting construction of fusion proteins |
| Comments: | A plasmid vector for screening promoters by determining beta-galactosidase activity (lacZ). Escherichia coli MC1000 = F- araD139 delta(ara, leu)7697 delta(lac)chi74 galU- galK- rpsL. The cloning sites in this vector are 5 to a promoterless beta-galactosidase gene. The insert must provide the promoter, the ribosome binding site, and/or the ATG translation initiation codon for activity to be expressed. |
| Media: | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions: | Temperature: 37.0°C |
| References: | Shultz J, et al. A previously unidentified gene in the spc operon of Escherichia coli K12 specifies a component of the protein export machinery. Cell 31: 227-235, 1982. PubMed: 6297749 Berman ML. Vectors for constructing hybrid genes. BioTechniques 1: 178-183, 1983. |
| Shipped: | freeze-dried |