宁波泰斯拓生物

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YEp356R plasmid in

货号 TS196731
中文名称 null
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产品简介
购买须知
产品名称: YEp356R plasmid in E. coli
商品货号: TS196731
Designations: YEp356R plasmid in E. coli
Depositors: CJ Lusty
Biosafety Level: 1
Host: Escherichia coli HB101
Vector Information:
Size (kb): 8.00xa0
Vector: YEp356R (plasmid)
Promoters: Promoter none
Construction: YEp356 (ATCC® 37731™), pUC18
Marker(s): URA3, ampR
Polylinker sites:xa0HindIII SphI PstI SalI XbaI BamHI SmaI KpnI SacI EcoRI
Possible host: Escherichia coli MC1061 (delta lacZ)

Features:
insert detection:
lacZ
marker(s): ampR, URA3
promoter: none
replicon: pMB1, 2 micron
Vector type: plasmid
Applications:
YE-type (episomal) shuttle vector
promoter-cloning vector
shuttle vector
Comments: This is one of 3 promoter-cloning, YE-type shuttle vectors (ATCC® No. 37737-37739™) with URA3 selection in Saccharomyces cerevisiae, a beta-galactosidase reporter gene and multiple cloning sites differing in reading frame.xa0 The sequence and reading frame of the multiple cloning sequence is: 5’ AAGCT TGC ATG CCT GCA GGT CGA CTC TAG AGG ATC CCC GGG TAC CGA GCT CGA ATT CCC AGC TTC GAT CCC 3’ from nucleotide 1 of the MCS through CCC for amino acid 8 of beta-galactosidase. Cloning into the HindIII, SphI, PstI SalI or XbaI sites leads to a TAG stop codon within the downstream XbaI site of the multiple cloning region.

The cleavage position in the reading frame for cloning sites is (where 3= between triplets): HindIII-2; SphI-3; PstI-3; SalI-2; XbaI-2; BamHI-2; SmaI-3; KpnI-3; SacI-3; EcoRI-2. The SacI site is not unique.

Restriction digests of the clone give the following sizes (kb): HindIII--8.0; EcoRI--8.0; BamHI--8.0; PstI--8.0; SalI--8.0.
Media: ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Growth Conditions:
Temperature: 37°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
Shipping Information: in E. coli containing the plasmid