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pOTC [pHOC]
pOTC [pHOC]
規(guī)格:
貨期:
編號(hào):B200847
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
pOTC [pHOC]
商品貨號(hào)
B200847
Designations
pOTC [pHOC]
Species
Homo sapiens, human
Depositors
KE Davies
Vector
Construct size (kb): 4.199999809265137
Insert
DNA: cDNA
Insert lengths(kb): 1.200000047683716
Gene product: ornithine carbamoyltransferase [OTC]
Alleles: C1, C2
Insert Size (kb)
1.200
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): PstI--3.0, 1.2; BamHI--4.2; HindIII--4.2; AvaI--3.2, 1.0; PvuII--3.0, 1.2.
Shows linkage with X-linked retinitis pigmentosa (theta = 0.06, LOD score = 5.69).
This probe is not a full-length cDNA. It is informative in the prenatal diagnosis of DMD.
References

Musarella MA, et al. Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis. Am. J. Hum. Genet. 43: 484-494, 1988. PubMed: 2902787

Francke U, et al. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions. Am. J. Hum. Genet. 40: 212-227, 1987. PubMed: 2883886

Davies KE, et al. Gene for OTC: Characterization and linkage to Duchenne muscular dystrophy. Nucleic Acids Res. 13: 155-165, 1985. PubMed: 3839070

Pembrey ME, et al. Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probe. J. Med. Genet. 22: 462-465, 1985. PubMed: 3001312

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