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微信小章| 产品名称： | pX65H7 |
|---|---|
| 商品货号： | TS161395 |
| Designations： | pX65H7 |
| Species： | Homo sapiens, human |
| Applications： | Enzyme(s) not detecting polymorphism: EcoRI, XbaI, SstI (tested against 6 X chromosomes showing the HindIII polymorphism). |
| Vector： | Construct size (kb): 5.150000095367432 |
| Insert： | DNA: genomic Insert lengths(kb): 0.699999988079071 Tissue: DNA from mouse/human AHA-11a hybrid line (X only) Gene product: DNA Segment, single copy DXS72 Alleles: A1, A2 |
| Insert Size (kb)： | 0.700 |
| 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): HindIII--4.5, 0.7; BamHI--5.1; PstI--5.1; PvuII--5.1; EcoRI--5.3; BamHI/EcoRI--4.0, 1.1. This probe is derived from X65 (genomic lambda phage clone). This probe is tightly linked to TCD. It is deleted in XL-62 family. DXS72 is linked to choroideremia with theta max = 0.02, LOD score = 7.09. Linked to X-linked hypohidrotic ectodermal dysplasia (theta = 0.02, Z = 11.38). There are no sites in the insert for BamHI, ClaI, EcoRI, EcoRV, NruI, PstI, PvuII, SalI, AvaI, BalI, NdeI, HpaI, SstI, XbaI, XhoI. There is KpnI site in the insert about 20 bp from the HindIII site nearer the vector BamHI site. HindIII polymorphism tested in X chromosomes from Caucasians, Blacks, and cell lines. Demonstrated X-linked segregation in 3 Caucasian families. Enzyme(s) not detecting polymorphism: EcoRI, XbaI, SstI (tested against 6 X chromosomes showing the HindIII polymorphism). |
| References： | Schmeckpeper BJ, et al. An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22. Nucleic Acids Res. 13: 5724, 1985. PubMed: 4041033 Merry DE, et al. Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21. Am. J. Hum. Genet. 45: 530-540, 1989. PubMed: 2491012 Lesko JG, et al. Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: Application to mapping the choroideremia locus. Am. J. Hum. Genet. 40: 303-311, 1987. PubMed: 2883887 Zonana J, et al. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis. Am. J. Hum. Genet. 43: 75-85, 1988. PubMed: 3163892 |