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cX5.7
cX5.7
規(guī)格:
貨期:
編號:B227572
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 cX5.7
商品貨號 B227572
Designations cX5.7
Species Homo sapiens, human
Depositors MH Hofker, E Bakker
Applications
Random prime labeling of the entire plasmid is recommended.
Vector
Construct size (kb): 2.799999952316284
Insert
DNA: genomic
Insert lengths(kb): 0.2000000029802322
Tissue: DNA from hamster/human hybrid cell line (X only)
Gene product: DNA Segment, single copy [DXS148]
Alleles: A2, A1
Insert Size (kb) 0.200
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/HindIII--2.7, 0.21.
The probe is difficult to work with. Random prime labeling of the entire plasmid is recommended.
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

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

Hofker MH, et al. Isolation of a random cosmid clone, CX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy. Hum. Genet. 74: 275-279, 1986. PubMed: 2877936

M H Hofker, personal communication

梅經(jīng)理 17280875617 1438578920
胡經(jīng)理 13345964880 2438244627
周經(jīng)理 17757487661 1296385441
于經(jīng)理 18067160830 2088210172
沈經(jīng)理 19548299266 2662369050
李經(jīng)理 13626845108 972239479
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