L1.28 (ATCC® 57302)

Organism: Homo sapiens, human  /  Clone Type: Clone  / 

Permits and Restrictions

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Designations L1.28
Species Homo sapiens, human
Vector
Construct size (kb): 4.199999809265137
Insert
DNA: genomic
Insert lengths(kb): 1.25
Gene product: DNA Segment, single copy [DXS7]
Alleles: A2, A1
Insert Size (kb) 1.25
Media Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Biosafety Level 1
Shipping Information Distributed: freeze-dried
Comments
Restriction digests of the clone give the following sizes (kb): EcoRI--2.9, 1.4; BglI--4.2; PvuII--4.2; HindIII--3.9, 0.48; PvuI--4.2.
References

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

Greer WL, et al. Linkage relationships of the Wiskott-Aldrich Syndrome to 10 loci in the pericentromeric region of the human X chromosome. Genomics 6: 568-571, 1990. PubMed: 2328995

Wieacker P, et al. Towards a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. Am. J. Hum. Genet. 36: 265-276, 1984. PubMed: 6324578

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

Musarella MA, et al. Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3. Genomics 5: 727-737, 1989. PubMed: 2574143

Derom C, et al. Zygosity determination in newborn twins using DNA variants. J. Med. Genet. 22: 279-282, 1985. PubMed: 2995674

Skolnick MH, Francke U. Report of the committee on human gene mapping by recombinant DNA techniques. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. Cytogenet. Cell Genet. 32: 194-204, 1982. PubMed: 7140362

European Society of Human Genetics. Abstracts from symposium on 'X- linked diseases'. Madrid, Spain, September 29-October 2, 1982. Clin. Genet. 23: 195-259, 1983. PubMed: 6682728

Peacocke M, Siminovitch KA. Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome. Proc. Natl. Acad. Sci. USA 84: 3430-3433, 1987. PubMed: 3472214

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