| 产品名称： | pYNZ23 |
|---|---|
| 商品货号： | TS140805 |
| Designations： | pYNZ23 |
| Species： | Homo sapiens, human |
| Applications： | For the MspI polymorphism, codominant segregation has been observed in 39 3-generation families. |
| Insert： | DNA: genomic Insert lengths(kb): 3.700000047683716 Gene product: DNA Segment, single copy D1S58 Alleles: A1, A2, B1, B2, C1, C2, D2, D1 |
| Insert Size (kb)： | 3.700 |
| 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/HindIII--2.7, 1.2, 1.0, 0.8, 0.7. The insert and restriction digests do not match those described in the references but do match the original deposited DNA. Subcloned from cosmid cYNZ23 isolated with a zetaglobin oligonucleotide. For the MspI polymorphism, codominant segregation has been observed in 39 3-generation families. |
| References： | Nakamura Y, et al. Isolation and mapping of a polymorphic DNA sequence pYNZ23 to chromosome 1 (D1S58). Nucleic Acids Res. 15: 9620, 1987. PubMed: 2446266 Murray JC, et al. Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome 1q. Am. J. Hum. Genet. 46: 486-491, 1990. PubMed: 2309700 Buetow KH, et al. A detailed multipoint gene map of chromosome 1q. Genomics 8: 13-21, 1990. PubMed: 1981991 Dracopoli NC, et al. The CEPH consortium linkage map of human chromosome 1. Genomics 9: 686-700, 1991. PubMed: 2037294 Nakamura Y, et al. Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 235: 1616-1622, 1987. PubMed: 3029872 |
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： | pYNZ23 |
|---|---|
| 商品货号： | TS140805 |
| Designations： | pYNZ23 |
| Species： | Homo sapiens, human |
| Applications： | For the MspI polymorphism, codominant segregation has been observed in 39 3-generation families. |
| Insert： | DNA: genomic Insert lengths(kb): 3.700000047683716 Gene product: DNA Segment, single copy D1S58 Alleles: A1, A2, B1, B2, C1, C2, D2, D1 |
| Insert Size (kb)： | 3.700 |
| 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/HindIII--2.7, 1.2, 1.0, 0.8, 0.7. The insert and restriction digests do not match those described in the references but do match the original deposited DNA. Subcloned from cosmid cYNZ23 isolated with a zetaglobin oligonucleotide. For the MspI polymorphism, codominant segregation has been observed in 39 3-generation families. |
| References： | Nakamura Y, et al. Isolation and mapping of a polymorphic DNA sequence pYNZ23 to chromosome 1 (D1S58). Nucleic Acids Res. 15: 9620, 1987. PubMed: 2446266 Murray JC, et al. Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome 1q. Am. J. Hum. Genet. 46: 486-491, 1990. PubMed: 2309700 Buetow KH, et al. A detailed multipoint gene map of chromosome 1q. Genomics 8: 13-21, 1990. PubMed: 1981991 Dracopoli NC, et al. The CEPH consortium linkage map of human chromosome 1. Genomics 9: 686-700, 1991. PubMed: 2037294 Nakamura Y, et al. Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 235: 1616-1622, 1987. PubMed: 3029872 |
