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pB24
pB24
規(guī)格:
貨期:
編號:B233275
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

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凍干粉
斜面
甘油
平板


產(chǎn)品名稱 pB24
商品貨號 B233275
Designations pB24
Species Homo sapiens, human
Vector
Construct size (kb): 4.650000095367432
Insert
DNA: genomic
Insert lengths(kb): 0.449999988079071
Gene product: DNA Segment, single copy [DXS67]
Alleles: B1, B2
Insert Size (kb) 0.450
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): PvuII--2.4, 2.3; BamHI--4.65; HindIII--4.65; EcoRI--4.65; EcoRI/HindIII--4.2, 0.45.
This marker shows linkage with Nance-Horan syndrome (theta = 0, LOD score = 2.74).
The BstNI RFLP is also recognized by MspI, but BstNI is less subject to partials.
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

Pillers DA, et al. Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy. Am. J. Hum. Genet. 47: 795-801, 1990. PubMed: 2220819

Monaco AP, et al. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy. Hum. Genet. 75: 221-227, 1987. PubMed: 2881877

Louis M Kunkel, personal communication

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