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J-Bir [pERT87-J-Bir]
J-Bir [pERT87-J-Bir]
規(guī)格:
貨期:
編號(hào):B225422
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 J-Bir [pERT87-J-Bir]
商品貨號(hào) B225422
Designations J-Bir [pERT87-J-Bir]
Species Homo sapiens, human
Depositors LM Kunkel
Vector
Construct size (kb): 6.21999979019165
Insert
DNA: genomic
Insert lengths(kb): 3.0
Gene product: DNA Segment, single copy (within DMD gene) [DXS270]
Alleles: A2, A1
Insert Size (kb) 3.0
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): HindIII/KpnI--3.3, 1.94, 1.25; HindIII--3.45, 3.2; BamHI--4.0, 2.8; KpnI--4.36, 2.03; consistent with deposited DNA.
The fragment is within the DMD locus.
A HindIII/KpnI digestion yields 2 fragments--one at 1.8-1.9 and the other at 1.15. The latter detects the RFLP, the former is slightly repeated.
The polymorphisms detected by this probe are contained within the DMD locus.
Care should be taken to assure efficient transfer of the larger allele.
References

Koenig M, et al. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50: 509-517, 1987. PubMed: 3607877

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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