微信小陈
微信小章| 产品名称： | St1 |
|---|---|
| 商品货号： | TS149345 |
| Designations： | St1 |
| Species： | Homo sapiens, human |
| Vector： | Construct size (kb): 10.19999980926514 |
| Insert： | DNA: genomic Insert lengths(kb): 6.0 Gene product: DNA Segment, single copy DXS86 Alleles: A1, A2 |
| Insert Size (kb)： | 6.0 |
| 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): EcoRI--6.78, 4.47; HindIII--12.26, 0.44; BamHI--6.07, 4.59; PstI--4.4, 3.7, 1.8, 0.79; PvuII--7.0, 2.97, 0.71. The depositor recommends hybridization in 50% formamide at 42C and washing at 65C, 0.5X SSC, 0.1% SDS. |
| References： | Mandel JL, et al. Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences. Cold Spring Harbor Symp. Quant. Biol. 51: 195-203, 1986. PubMed: 3472716 Oberle I, et al. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. Hum. Genet. 77: 60-65, 1987. PubMed: 3502701 Reilly DS, et al. Genetic and physical mapping of Xq24-q26 markers flanking the Lowe oculocerebrorenal syndrome. Genomics 8: 62-70, 1990. PubMed: 2081601 Jean Louis Mandel, personal communication |