| 产品名称： | pHRnES1.9 |
|---|---|
| 商品货号： | TS145751 |
| Designations： | pHRnES1.9 |
| Species： | Homo sapiens, human |
| Depositors： | JM Chirgwin |
| Vector： | Construct size (kb): 4.599999904632568 |
| Insert： | DNA: genomic Insert lengths(kb): 1.899999976158142 Gene product: renin REN Alleles: H1, H2, J1, B1, B2, F1, F2, G1, K1, K2, G2, I1 |
| Insert Size (kb)： | 1.900 |
| 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/PstI--2.7, 1.9; HindIII--4.6; PstI--4.6; BamHI--4.6. Evidence of linkage (theta = 0.02, LOD score = 9.09) was found between the renin (REN) gene on 1q and Van der Woude syndrome (VWS). This probe is unique in sequence and contains exons 7 - 10 of human renin. There is a short 9 bp exon which has been identified that lies between exon 5 and the former exon 6. BglI, HindIII, BglII, TaqI, RsaI, and BstXI RFLPs are detected with a mix of the inserts from pHRnX0.8 (ATCC 57174), pHRnX3.6 (ATCC 57178), and pHRnES1.9 (TS145751), apparently from base changes not within the coding regions of the gene. Detection of the HindIII polymorphism (alleles 8.7 and 6.2 kb) was verified by CEPH. Enzyme(s) not detecting polymorphism: EcoRI, BanI, MlnI, BstEII, HphI, MspI, SstI, DraI, PvuII, MboII, ApaI, SinI, NciI, ScaI, XbaI, HinfI, NdeI, HincII. XmnI and PstI give uninterpretable results. Tested on a small sample. |
| References： | Naftilan AJ, et al. A lack of genetic linkage of renin gene restriction fragment length polymorphisms with human hypertension. Hypertension 14: 614-618, 1989. PubMed: 2573574 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 Chirgwin JM, et al. Human renin gene is on chromosome 1. Somatic Cell Mol. Genet. 10: 415-421, 1984. PubMed: 6379904 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 Hobart PM, et al. Human renin gene: Structure and sequence analysis. Proc. Natl. Acad. Sci. USA 81: 5026-5030, 1984. PubMed: 6089171 John M Chirgwin, 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： | pHRnES1.9 |
|---|---|
| 商品货号： | TS145751 |
| Designations： | pHRnES1.9 |
| Species： | Homo sapiens, human |
| Depositors： | JM Chirgwin |
| Vector： | Construct size (kb): 4.599999904632568 |
| Insert： | DNA: genomic Insert lengths(kb): 1.899999976158142 Gene product: renin REN Alleles: H1, H2, J1, B1, B2, F1, F2, G1, K1, K2, G2, I1 |
| Insert Size (kb)： | 1.900 |
| 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/PstI--2.7, 1.9; HindIII--4.6; PstI--4.6; BamHI--4.6. Evidence of linkage (theta = 0.02, LOD score = 9.09) was found between the renin (REN) gene on 1q and Van der Woude syndrome (VWS). This probe is unique in sequence and contains exons 7 - 10 of human renin. There is a short 9 bp exon which has been identified that lies between exon 5 and the former exon 6. BglI, HindIII, BglII, TaqI, RsaI, and BstXI RFLPs are detected with a mix of the inserts from pHRnX0.8 (ATCC 57174), pHRnX3.6 (ATCC 57178), and pHRnES1.9 (TS145751), apparently from base changes not within the coding regions of the gene. Detection of the HindIII polymorphism (alleles 8.7 and 6.2 kb) was verified by CEPH. Enzyme(s) not detecting polymorphism: EcoRI, BanI, MlnI, BstEII, HphI, MspI, SstI, DraI, PvuII, MboII, ApaI, SinI, NciI, ScaI, XbaI, HinfI, NdeI, HincII. XmnI and PstI give uninterpretable results. Tested on a small sample. |
| References： | Naftilan AJ, et al. A lack of genetic linkage of renin gene restriction fragment length polymorphisms with human hypertension. Hypertension 14: 614-618, 1989. PubMed: 2573574 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 Chirgwin JM, et al. Human renin gene is on chromosome 1. Somatic Cell Mol. Genet. 10: 415-421, 1984. PubMed: 6379904 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 Hobart PM, et al. Human renin gene: Structure and sequence analysis. Proc. Natl. Acad. Sci. USA 81: 5026-5030, 1984. PubMed: 6089171 John M Chirgwin, personal communication |
