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pHSG-cre
pHSG-cre
規(guī)格:
貨期:
編號:B201794
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 pHSG-cre
商品貨號 B201794
Designations pHSG-cre
Depositors ML Pall
Biosafety Level 1
Host
Distribution host: Escherichia coli JM109
Vector Information
Size (kb): 4.0000000000000000
DESCRIPTION OF VECTOR COMPONENT:
Name of vector: pHSG298
Intact vector size: 2.676
Type of vector: plasmid
Vector end: EcoRI
Vector end: SalI
Cloning sites: EcoRI SacI KpnI SmaI BamHI XbaI SalI PstI SphI
Polylinker sites: EcoRI SacI KpnI SmaI BamHI XbaI SalI PstI SphI HindIII
Other unique sites: ClaI
Construction: pHSG1339
Host range: Escherichia coli
Features (with orientation and position when available):
marker(s): kanR, ->
insert detection: lacZ', <-
MCS: HindIII...EcoRI, ->
replicon: pSC101
Cross references:
Vector: pHSG-cre (plasmid)
Promoters: Promoter lac
Construction: pHSG298, lambdaKC
Marker(s):kanR
Construct size (kb): 4.0
Features: marker(s): kanR
other: cre
promoter: lac
replicon: pMB1
Applications
produces protein recombinase, site-specific
vector for other uses
Comments
Restriction digests of the clone give the following sizes (kb): EcoRI/SalI--2.6, 1.4; EcoRI--4.0; PstI--2.6, 1.4.
The cre gene contains the following restriction sites (approximate kb from the 5' end): BamHI--0.84; ClaI--1.29.
The lambda/plasmid hybrid vectors can then be used for automatic subcloning; that is, the cre-mediated excision of plasmid constructs.
A plasmid useful for generating novel lambda/plasmid hybrid vectors by using cre-lox recombination to exchange new plasmids for plasmids already in lambda/plasmid hybrids.
Constructed by ligating a 1.3 kb cre-containing fragment from lambdaKC to pHSG298 digested with EcoRI+SalI.
Media ATCC® Medium 1236: LB Medium (ATCC medium 1065) with 25 mcg/ml kanamycin
Growth Conditions
Temperature: 37.0°C
References

Elledge SJ, et al. lambdaYES: a multifunctional cDNA expression vector for the isolation of genes by complementation of yeast and Escherichia coli mutations. Proc. Natl. Acad. Sci. USA 88: 1731-1735, 1991. PubMed: 1848010

Brunelli JP, Pall ML. Lambda/Plasmid vector construction by in vivo cre/lox-mediated recombination. BioTechniques 16: 1060-1064, 1994. PubMed: 8074871

Takeshita S, et al. High-copy-number and low-copy-number plasmid vectors for lacZalpha-complementation and chloramphenicol- or kanamycin-resistance selection. Gene 61: 63-74, 1987. PubMed: 3327753

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