YEp356-质粒载体-ATCC-DSM-CCUG-泰斯拓生物

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YEp356
YEp356
规格:
货期:
编号:TS147100
品牌:Testobio
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
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YEp356

  • 货号: TS147100
  • 好评
有货
  • 品牌 : TESTOBIO
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
合作单位: