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782 [L782]
782 [L782]
規(guī)格:
貨期:
編號:B241876
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 782 [L782]
商品貨號 B241876
Designations 782 [L782]
Species Homo sapiens, human
Vector
Construct size (kb): 6.199999809265137
Insert
DNA: genomic
Insert lengths(kb): 3.400000095367432
Gene product: DNA Segment, single copy [DXS85]
Alleles: A2, A1
Insert Size (kb) 3.400
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: 200 ng)
Comments
Restriction digests of the clone give the following sizes (kb): BamHI--3.3, 3.0; HindIII--3.4, 2.8; EcoRI--6.2; BglI--3.4, 2.9; PvuI--6.2.
There is tight linkage between DXS197 and DXS85 (theta = 0, LOD score = 4.14).
The insert was isolated from a phage library derived from flow-sorted X chromosomes.
References

Hofker MH, et al. The X-chromosome shows less genetic variation at restriciton sites than the autosomes. Am. J. Hum. Genet. 39: 438-451, 1986. PubMed: 2876629

Bakker E, et al. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet 1: 655-658, 1985. PubMed: 2858615

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

Lagerstrom M, et al. Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis. Am. J. Hum. Genet. 46: 120-125, 1990. PubMed: 1967204

Hofker MH, et al. Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: Potential use for diagnosis of Duchenne muscular dystrophy. Hum. Genet. 70: 148-156, 1985. PubMed: 2989153

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