pRS306 phagemid in E. coli
pRS306 phagemid in E. coli
规格:
货期:
编号:TS148376
品牌:Testobio
| 产品名称： | pRS306 phagemid in E. coli |
|---|---|
| 商品货号： | TS148376 |
| Designations： | pRS306 phagemid in E. coli |
| Depositors： | P Hieter |
| Biosafety Level： | 1 |
| Vector Information： | Size (kb): 4.381 Vector: pRS306 (phagemid) Promoters: Promoter T3 Construction: pRSS56 pBluescript KS+, pBS(+) Marker(s):URA3,ampR Construct size (kb): 4.381 Features: insert detection: lacZ marker(s): ampR, URA3 promoter: lac, T3, T7 replicon: pMB1, f1 |
| Applications： | YI-type (integrating) shuttle vector shuttle vector vector containing primer sites useful for sequencing vector permitting RNA synthesis in vitro vector permitting production of single-stranded DNA vector permitting visual detection of recombinants |
| Comments： | Restriction digests of the clone give the following sizes (kb): PstI--2.7, 1.65; PvuI--3.9, 0.40; EcoRI--4.4; HindIII--4.4. One of a series of pBluescript-based integrating vectors (ATCC 77138-77141) differing in the yeast selectable marker gene. YI-type integrating shuttle vector permitting visual detection of recombinants and production of ssDNA in E. coli. Contains promoters for in vitro RNA synthesis, priming sites useful for sequencing, and encodes the lacZ alpha (lacZ) peptide. pRSS56, constructed by ligating a PvuI fragment (bp 498-2412) of pBluescript KS+ to a PvuI fragment (bp 2850-730) of pBS(+), contains the KS MCS from pBluescript KS+ and the unique NdeI and AatII sites between bla and f1 origin of pBS(+). A fragment (1.112 kb) containing the URA3 gene was inserted into the NdeI site of pRSS56. All ends were blunted. The order of the major features in this plasmid is: URA3 - f1 ori (NaeI) - T7 promoter - lacZ/MCS - T3 promoter - pMB1 ori - bla. The following restriction sites in the multiple cloning site (MCS) are no longer unique: ApaI EcoRV PstI. |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions： | Temperature: 37.0°C |
| References： | Sikorski RS, Hieter P. A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. Genetics 122: 19-27, 1989. PubMed: 2659436 |
| Related Products： | component of:ATCC 77189 |
| Shipped： | frozen |
| Shipping Information： | Glycerol stock of E. coli containing the plasmid |
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pRS306 phagemid in E. coli
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| 产品名称： | pRS306 phagemid in E. coli |
|---|---|
| 商品货号： | TS148376 |
| Designations： | pRS306 phagemid in E. coli |
| Depositors： | P Hieter |
| Biosafety Level： | 1 |
| Vector Information： | Size (kb): 4.381 Vector: pRS306 (phagemid) Promoters: Promoter T3 Construction: pRSS56 pBluescript KS+, pBS(+) Marker(s):URA3,ampR Construct size (kb): 4.381 Features: insert detection: lacZ marker(s): ampR, URA3 promoter: lac, T3, T7 replicon: pMB1, f1 |
| Applications： | YI-type (integrating) shuttle vector shuttle vector vector containing primer sites useful for sequencing vector permitting RNA synthesis in vitro vector permitting production of single-stranded DNA vector permitting visual detection of recombinants |
| Comments： | Restriction digests of the clone give the following sizes (kb): PstI--2.7, 1.65; PvuI--3.9, 0.40; EcoRI--4.4; HindIII--4.4. One of a series of pBluescript-based integrating vectors (ATCC 77138-77141) differing in the yeast selectable marker gene. YI-type integrating shuttle vector permitting visual detection of recombinants and production of ssDNA in E. coli. Contains promoters for in vitro RNA synthesis, priming sites useful for sequencing, and encodes the lacZ alpha (lacZ) peptide. pRSS56, constructed by ligating a PvuI fragment (bp 498-2412) of pBluescript KS+ to a PvuI fragment (bp 2850-730) of pBS(+), contains the KS MCS from pBluescript KS+ and the unique NdeI and AatII sites between bla and f1 origin of pBS(+). A fragment (1.112 kb) containing the URA3 gene was inserted into the NdeI site of pRSS56. All ends were blunted. The order of the major features in this plasmid is: URA3 - f1 ori (NaeI) - T7 promoter - lacZ/MCS - T3 promoter - pMB1 ori - bla. The following restriction sites in the multiple cloning site (MCS) are no longer unique: ApaI EcoRV PstI. |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions： | Temperature: 37.0°C |
| References： | Sikorski RS, Hieter P. A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. Genetics 122: 19-27, 1989. PubMed: 2659436 |
| Related Products： | component of:ATCC 77189 |
| Shipped： | frozen |
| Shipping Information： | Glycerol stock of E. coli containing the plasmid |
