微信小陈
微信小章| 产品名称： | RC8 |
|---|---|
| 商品货号： | TS142856 |
| Designations： | RC8 |
| Species： | Homo sapiens, human |
| Vector： | Construct size (kb): 9.399999618530273 |
| Insert： | DNA: genomic Insert lengths(kb): 6.099999904632568 Gene product: DNA Segment, single copy DXS9 Alleles: A3, A1, A2 |
| Insert Size (kb)： | 6.100 |
| 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： | Restriction digests of the clone give the following sizes (kb): EcoRI--6.0, 3.6; PstI--9.4; BamHI--5.1, 4.4; HindIII--4.1, 2.0, 1.7, 1.0, 0.5. This probe is linked to the retinoschisis gene, to ocular albinism, and apparently to the STS gene. |
| References： | Gellert G, et al. Linkage relationship between retinoschisis and four marker loci. Hum. Genet. 79: 382-384, 1988. PubMed: 2900804 Borresen AL, et al. DNA polymorphism of the RC8 probe on the X chromosome. Clin. Genet. 27: 411-413, 1985. PubMed: 2986884 Drayna D, et al. Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms. Proc. Natl. Acad. Sci. USA 81: 2836-2839, 1984. PubMed: 6326147 Schwartz CE, et al. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am. J. Hum. Genet. 47: 454-458, 1990. PubMed: 2393020 |