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
Construct size (kb): 4.199999809265137
DNA: genomic
Insert lengths(kb): 1.25
Gene product: DNA Segment, single copy [DXS7]
Alleles: A2, A1
Insert Size (kb) 1.25
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
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.

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