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pOTC [pHOC]
pOTC [pHOC]
規(guī)格:
貨期:
編號:B162219
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 B162219
Designations pOTC [pHOC]
Species Homo sapiens, human
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
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: DNA (dried). Rehydrate with TE. (amount: 2 ug)
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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