GM23885
LCL from B-Lymphocyte
Description:
HEMOGLOBIN F, HEREDITARY PERSISTENCE OF
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases
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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Country of Origin
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USA
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Family Member
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4
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Family History
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N
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Relation to Proband
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mother
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ISCN
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46,XX.arr 1p31.3(63571339-63844510)x3
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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 LINE assay |
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| Remarks |
Clinically unaffected; mother of affected daughter with non-deletional hereditary persistence of fetal hemoglobin; affected daughter is GM23883 (Lymph); unaffected daughter is GM23884 (Lymph); unaffected son is GM23886 (Lymph). |
| Split Ratio |
1:4 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| Percent O2 |
AMBIENT |
| Medium |
Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent |
| Serum |
15% fetal bovine serum Not Inactivated |
| Supplement |
- |
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