| 产品名称: | 26P |
|---|---|
| 商品货号: | TS154154 |
| Designations: | 26P |
| Species: | Homo sapiens, human |
| Depositors: | J Mandel |
| Vector: | Construct size (kb): 9.399999618530273 |
| Insert: | DNA: genomic Insert lengths(kb): 5.599999904632568 Tissue: lymphoblast (49,XXXXY) cell line Gene product: DNA Segment, single copy D9S5 Alleles: B1, B2, B3 |
| Insert Size (kb): | 5.600 |
| 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): PstI/SalI--5.6, 3.8; AvaI--3.5, 3.2, 1.44, 0.82 + smaller; EcoRI--9.4; BglI--7.55, 1.85; HindIII--9.4. The insert contains the following restriction sites (in approximate kb from the PstI site): NotI--0.44; BssHII--0.96. IMPORTANT: To prevent amplification of a rearranged and/or deleted cosmid, we recommend streaking on LB + amp plates at 30C and picking small colonies for liquid culture. This probe is approximately 15 kb from DR47. Detects genomic restriction fragments of the following sizes (complete digest, kb): NotI--450; EagI--260; BsshII--160; SacII--160. The ClaI and the BamHI sites of the polylinker are absent as a result of the probe construction. All other sites of the polylinker are retained. This was subcloned from the end of the cosmid c26 (Cos 26) by digestion with PstI and religation of the vector/insert construct at low DNA concentration. |
| References: | Fujita R, et al. Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia. Proc. Natl. Acad. Sci. USA 87: 1796-1800, 1990. PubMed: 1968638 Hanauer A, et al. The Friedreich ataxia gene is assigned to chromosoem 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15. Am. J. Hum. Genet. 46: 133-137, 1990. PubMed: 2294745 Fujita R, et al. Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field electrophoresis. Genomics 10: 915-920, 1991. PubMed: 1916823 Jean Louis Mandel, personal communication |