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微信小章| 产品名称： | pD2 |
|---|---|
| 商品货号： | TS133053 |
| Designations： | pD2 |
| Species： | Homo sapiens, human |
| Vector： | Construct size (kb): 5.0 |
| Insert： | DNA: genomic Insert lengths(kb): 0.8999999761581421 Tissue: lymphoblast (49,XXXXY) cell line Gene product: DNA Segment, single copy DXS43 Alleles: A1, A2 |
| Insert Size (kb)： | 0.900 |
| 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 distributed as 5 ug in 50 ul TE (volume: 50 ul, |
| Comments： | Restriction digests of the clone give the following sizes (kb): EcoRI--5.0; HindIII--5.0; PstI--5.0; BamHI--5.0; PvuII--5.0; HindIII/EcoRI--4.15, 0.87. Shows linkage with X-linked retinoschisis (theta = 0.02, LOD score = 13.87). This marker shows linkage with Nance-Horan syndrome (theta = 0, LOD score = 2.89). There is tight linkage between DXS197 and DXS43 (theta = 0.032, LOD score = 6.19). |
| References： | Alitalo T, et al. Linkage relationships and gene order around the locus for X-linked retinoschisis. Am. J. Hum. Genet. 43: 476-483, 1988. PubMed: 3177388 Aldridge J, et al. A strategy to reveal high-frequency RFLPs along the human X chromosome. Am. J. Hum. Genet. 36: 546-564, 1984. PubMed: 6328976 Stambolian D, et al. Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis. Am. J. Hum. Genet. 47: 13-19, 1990. PubMed: 1971992 Thakker RV, et al. Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families. Genomics 8: 189-193, 1990. PubMed: 1979046 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 |