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pSVA3
pSVA3
規格:
價格:
編號:B241866
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規格:
凍干粉
斜面
甘油
平板


產品名稱
pSVA3
商品貨號
B241866
Designations
pSVA3
Species
Cricetulus griseus, hamster, Chinese
培養基
Depositors
PW Melera
Applications
in another host, produces protein dihydrofolate reductase
Vector
Construct size (kb): 5.099999904632568
DESCRIPTION OF VECTOR COMPONENT:
Name of vector: pSV2-neo
Intact vector size: 5.729
Type of vector: plasmid
Vector end: HindIII
Vector end: SmaI
Cloning sites: EcoRI BamHI PvuII PstI HindIII
Polylinker sites:
Construction: SV40, Tn5, pBR322
Host range: vertebrate cells; Escherichia coli
Features (with orientation and position when available):
replicon: SV40
marker(s): G418R, <-
restriction site: HindIII
promoter: SV40 early, <-
replicon: pMB1
marker(s): ampR, <-
Cross references: DNA Seq. Acc.: U02434
Insert
DNA: cDNA
DESCRIPTION OF INSERT COMPONENT:
Genome: hamster, Chinese
Gene symbol: DHFR
Gene name: dihydrofolate reductase
Contains complete coding sequence?: U
Tissue: lung cell line
Type of DNA: cDNA
Insert 5' end: HindIII
Insert 3' end: BglII
Insert size (kb): 0.71
Cross references:

Insert information:

Insert size (kb): 0.71

DNA : cDNA

Gene : DHFR

Source : hamster, Chinese lung cell line

Insert lengths(kb): 0.7099999785423279
Tissue: lung cell line
Gene product: dihydrofolate reductase [DHFR]
Target Gene: dihydrofolate reductase
Insert Size (kb)
0.710
Media
ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Biosafety Level
1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Shipping Information
Distributed: freeze-dried
Comments
Restriction digests of the clone give the following sizes (kb): BamHI--3.5, 1.7; EcoRI--2.7, 2.3; PstI--1.9, 1.4, 0.95, 0.9; PvuII--4.0, 1.1; HindIII/SmaI--5.2.
Transfected cells amplify DHFR sequences.
Encodes the L22F mutant of DHFR that can serve as a dominant selection marker because it retains catalytic activity and also confers methotrexate (MTX) resistance at low MTX concentrations (125 nM).
Constructed by cloning a HindIII/SmaI fragment containing the gene into pSV2-neo from which neoR had been removed. This plasmid was then cut with SmaI and BglII to remove 18 G nucleotides at the 3' end.
The BglII site was filled in, and ligated to the SmaI site, thereby destroying the original BglII and SmaI sites.
Removing the HindIII/SmaI fragment from pSV2-neo removes all but the 3' 171 bp of neoR.
References

Hussain A, et al. Construction of a dominant selectable marker using a novel dihydrofolate reductase. Gene 112: 179-188, 1992. PubMed: 1555767

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