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產(chǎn)品名稱(chēng)	pD2
商品貨號(hào)	B243878
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

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