| 产品名称： | pOTC pHOC |
|---|---|
| 商品货号： | TS176058 |
| 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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| 产品名称： | pOTC pHOC |
|---|---|
| 商品货号： | TS176058 |
| 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 |
