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微信小章| 产品名称： | pXUT-23 pXUT23 |
|---|---|
| 商品货号： | TS152232 |
| Designations： | pXUT-23 pXUT23 |
| Species： | Homo sapiens, human |
| Depositors： | KE Davies, HF Willard |
| Vector： | Construct size (kb): 4.900000095367432 |
| Insert： | DNA: genomic Insert lengths(kb): 2.099999904632568 Gene product: DNA Segment, single copy DXS16 Alleles: B1, B1, B2, B2, A1, A2 |
| Insert Size (kb)： | 2.100 |
| 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): BamHI--2.7, 2.2; SalI--4.8, PstI--4.2, 0.6; EcoRI--4.9; AccI--4.9. Enzyme(s) not detecting polymorphism: PvuII. |
| References： | de Martinville B, Uhrhammer NA. BclI RFLP at the DXS16 locus. Nucleic Acids Res. 16: 10949, 1988. PubMed: 2905045 Bakker E, et al. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet 1: 655-658, 1985. PubMed: 2858615 Davies KE, et al. Physical mapping of RFLPs surrounding the Duchenne muscular dystrophy locus. Cytogenet. Cell Genet. 40: 613, 1985. Schwartz CE, et al. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am. J. Hum. Genet. 47: 454-458, 1990. PubMed: 2393020 |