| 产品名称： | p99-6 |
|---|---|
| 商品货号： | TS162885 |
| Designations： | p99-6 |
| Species： | Homo sapiens, human |
| Depositors： | LM Kunkel, SA Latt |
| Applications： | Multipoint linkage analysis shows complete linkage (LOD score = 7.07). |
| Vector： | Construct size (kb): 4.050000190734863 |
| Insert： | DNA: genomic Insert lengths(kb): 1.399999976158142 Tissue: lymphoblast (49,XXXXY) cell line Gene product: DNA Segment, single copy DXS41 Alleles: A1, A2 |
| Insert Size (kb)： | 1.400 |
| 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： | This marker shows linkage with Nance-Horan syndrome (theta = 0, LOD score = 3.44). Multipoint linkage analysis shows complete linkage (LOD score = 7.07). |
| References： | 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 Schwartz CE, et al. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am. J. Hum. Genet. 47: 454-458, 1990. PubMed: 2393020 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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| 产品名称： | p99-6 |
|---|---|
| 商品货号： | TS162885 |
| Designations： | p99-6 |
| Species： | Homo sapiens, human |
| Depositors： | LM Kunkel, SA Latt |
| Applications： | Multipoint linkage analysis shows complete linkage (LOD score = 7.07). |
| Vector： | Construct size (kb): 4.050000190734863 |
| Insert： | DNA: genomic Insert lengths(kb): 1.399999976158142 Tissue: lymphoblast (49,XXXXY) cell line Gene product: DNA Segment, single copy DXS41 Alleles: A1, A2 |
| Insert Size (kb)： | 1.400 |
| 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： | This marker shows linkage with Nance-Horan syndrome (theta = 0, LOD score = 3.44). Multipoint linkage analysis shows complete linkage (LOD score = 7.07). |
| References： | 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 Schwartz CE, et al. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am. J. Hum. Genet. 47: 454-458, 1990. PubMed: 2393020 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 |
