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pD2
pD2
規(guī)格:
貨期:
編號(hào):B243878
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 pD2
商品貨號(hào) B243878
Designations pD2
Species Homo sapiens, human
Vector
Construct size (kb): 5.0
Insert
DNA: genomic
Insert lengths(kb): 0.8999999761581421
Tissue: lymphoblast (49,XXXXY) cell line
Gene product: DNA Segment, single copy [DXS43]
Alleles: A1, A2
Insert Size (kb) 0.900
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 distributed as 5 ug in 50 ul TE (volume: 50 ul,
Comments
Restriction digests of the clone give the following sizes (kb): EcoRI--5.0; HindIII--5.0; PstI--5.0; BamHI--5.0; PvuII--5.0; HindIII/EcoRI--4.15, 0.87.
Shows linkage with X-linked retinoschisis (theta = 0.02, LOD score = 13.87).
This marker shows linkage with Nance-Horan syndrome (theta = 0, LOD score = 2.89).
There is tight linkage between DXS197 and DXS43 (theta = 0.032, LOD score = 6.19).
References

Alitalo T, et al. Linkage relationships and gene order around the locus for X-linked retinoschisis. Am. J. Hum. Genet. 43: 476-483, 1988. PubMed: 3177388

Aldridge J, et al. A strategy to reveal high-frequency RFLPs along the human X chromosome. Am. J. Hum. Genet. 36: 546-564, 1984. PubMed: 6328976

Stambolian D, et al. Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis. Am. J. Hum. Genet. 47: 13-19, 1990. PubMed: 1971992

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

Francke U, et al. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions. Am. J. Hum. Genet. 40: 212-227, 1987. PubMed: 2883886

梅經(jīng)理 17280875617 1438578920
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周經(jīng)理 17757487661 1296385441
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李經(jīng)理 13626845108 972239479
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