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p99-6
p99-6
規(guī)格:
貨期:
編號:B206821
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 p99-6
商品貨號 B206821
Designations p99-6
Species Homo sapiens, human
Applications
Multipoint linkage analysis shows complete linkage (LOD score = 7.07).
Vector
Construct size (kb): 4.050000190734863
Insert
DNA: genomic
Insert lengths(kb): 1.399999976158142
Tissue: lymphoblast (49,XXXXY) cell line
Gene product: DNA Segment, single copy [DXS41]
Alleles: A1, A2
Insert Size (kb) 1.400
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
This marker shows linkage with Nance-Horan syndrome (theta = 0, LOD score = 3.44). Multipoint linkage analysis shows complete linkage (LOD score = 7.07).
References

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

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

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

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