| 产品名称： | C7 pC7 |
|---|---|
| 商品货号： | TS164560 |
| Designations： | C7 pC7 |
| Species： | Homo sapiens, human |
| Vector： | Construct size (kb): 7.199999809265137 |
| Insert： | DNA: genomic Insert lengths(kb): 2.799999952316284 Tissue: fibroblast GM1415 (48,XXXX) cell line Gene product: DNA Segment, single copy DXS28 Alleles: A1, A2 |
| Insert Size (kb)： | 2.800 |
| 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： | Restriction digests of the clone give the following sizes (kb): BamHI--7.0; EcoRI--4.4, 2.8; HindIII--4.6, 1.5, 0.78; PstI--7.0; HincII--3.2, 1.9, 1.2, 0.7. This probe is located 5-15 cM from the DMD locus. It is informative in the prenatal diagnosis of DMD. The depositor recommends an agarose gel at 0.9% or less to resolve the allelic fragments and washing conditions of 65C, 0.5X SSC, 0.1% SDS. The faint band at 3-4 kb is of autosomal origin. |
| References： | Oberle I, et al. Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome. Hum. Genet. 72: 43-49, 1986. PubMed: 3002952 Pillers DA, et al. Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy. Am. J. Hum. Genet. 47: 795-801, 1990. PubMed: 2220819 Schwartz CE, et al. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am. J. Hum. Genet. 47: 454-458, 1990. PubMed: 2393020 Thakker RV, et al. Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families. Genomics 8: 189-193, 1990. PubMed: 1979046 Jean Louis Mandel, personal communication |
产品中心 Product Center
联系我们CONTACT US
-
0574-87917803
24小时服务热线 -
testobio@163.com
销售邮箱 -
浙江省宁波市高新区晶辉路866弄33号智造港E4幢3楼
地址
联系方式
-
章丽敏
17757489010 -
朱静
18067106081 -
李晴
18067408036 -
李晶晶
13375187189 -
周雪
13372109301
| 产品名称： | C7 pC7 |
|---|---|
| 商品货号： | TS164560 |
| Designations： | C7 pC7 |
| Species： | Homo sapiens, human |
| Vector： | Construct size (kb): 7.199999809265137 |
| Insert： | DNA: genomic Insert lengths(kb): 2.799999952316284 Tissue: fibroblast GM1415 (48,XXXX) cell line Gene product: DNA Segment, single copy DXS28 Alleles: A1, A2 |
| Insert Size (kb)： | 2.800 |
| 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： | Restriction digests of the clone give the following sizes (kb): BamHI--7.0; EcoRI--4.4, 2.8; HindIII--4.6, 1.5, 0.78; PstI--7.0; HincII--3.2, 1.9, 1.2, 0.7. This probe is located 5-15 cM from the DMD locus. It is informative in the prenatal diagnosis of DMD. The depositor recommends an agarose gel at 0.9% or less to resolve the allelic fragments and washing conditions of 65C, 0.5X SSC, 0.1% SDS. The faint band at 3-4 kb is of autosomal origin. |
| References： | Oberle I, et al. Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome. Hum. Genet. 72: 43-49, 1986. PubMed: 3002952 Pillers DA, et al. Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy. Am. J. Hum. Genet. 47: 795-801, 1990. PubMed: 2220819 Schwartz CE, et al. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am. J. Hum. Genet. 47: 454-458, 1990. PubMed: 2393020 Thakker RV, et al. Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families. Genomics 8: 189-193, 1990. PubMed: 1979046 Jean Louis Mandel, personal communication |
