GM01261
LCL from B-Lymphocyte
Description:
18P- SYNDROME
TRANSLOCATED CHROMOSOME
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Chromosome Abnormalities |
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Biopsy Source
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Peripheral vein
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Cell Type
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B-Lymphocyte
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Tissue Type
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Blood
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Transformant
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Epstein-Barr Virus
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Sample Source
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LCL from B-Lymphocyte
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Race
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White
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Relation to Proband
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proband
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Confirmation
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Karyotypic analysis after cell line submission to CCR
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ISCN
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45,XX,der(13;18)(13qter>13q10::18q10>18qter)
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
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| Remarks |
HLA type A1,A2,Bw15(B18); 18p- syndrome |
| Markie D, Jones TA, Sheer D, Bodmer WF, A somatic cell hybrid panel for regional mapping of human chromosome 18. Genomics14:431-6 1992 |
| PubMed ID: 1427858 |
| |
| Nishisho I, Tateishi H, Motomura K, Miki T, Yoshida MC, Ikeuchi T, Yamamoto K, Okazaki M, Takai S, Mori T, Assignment of a polymorphic locus of OS-4(D18S5) DNA segment to human chromosome region 18q21.3----qter. Jinrui Idengaku Zasshi32:1-7 1987 |
| PubMed ID: 2886683 |
| |
| Kistenmacher, The association of autoimmune disorders with 18 p-syndrome. Am J Hum Genet26:49A (1974):1-7 1974 |
| PubMed ID: 2886683 |
| Split Ratio |
1:5 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| Medium |
Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent |
| Serum |
20% fetal bovine serum Not Inactivated |
| Substrate |
None specified |
| Subcultivation Method |
dilution - add fresh medium |
| Supplement |
- |
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