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| 产品名称： | p7F1 7F1 |
|---|---|
| 商品货号： | TS182831 |
| Designations： | p7F1 7F1 |
| Species： | Homo sapiens, human |
| Applications： | DXS42 shows tight linkage with Lowe oculocerebrorenal syndrome (OCRL) in seven families (no recombination was observed between DXS42 and OCRL). |
| Vector： | Construct size (kb): 4.5 |
| Insert： | DNA: genomic Insert lengths(kb): 1.799999952316284 Tissue: lymphoblast GM1416 (48,XXXX) cell line Gene product: DNA Segment, single copy DXS42 Alleles: A2, A1, C1, C2 |
| Insert Size (kb)： | 1.800 |
| 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： | Insert contains an internal BamHI site. Restriction digests of the clone give the following sizes (kb): BamHI--3.4, 1.0; EcoRI/HindIII--2.7, 1.8; HindIII--4.5; EcoRI--2.7. 1.8; PstI--3.3, 1.1. DXS42 shows tight linkage with Lowe oculocerebrorenal syndrome (OCRL) in seven families (no recombination was observed between DXS42 and OCRL). This probe was derived from a cosmid containing p43-15a. It is located 7-10 kb from p43-15. |
| References： | Reilly DS, et al. Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment. Am. J. Hum. Genet. 42: 748-755, 1988. PubMed: 2895982 |