GM11251
Fibroblast from Whole embryo, Embryo
Description:
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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Embryo
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Cell Type
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Fibroblast
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Tissue Type
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Whole embryo
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Transformant
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Untransformed
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Sample Source
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Fibroblast from Whole embryo, Embryo
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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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46,XY,t(7;17)(7pter>7p10::17p13.3> 17pter;17qter>17p13.3::7q10>7qter)
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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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| Passage Frozen |
3 |
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis |
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| Cytogenetics |
Chromosome 17: TRANSLOCATION Breakpoint 17p13 t(7;17)17p13 |
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Chromosome 7: TRANSLOCATION Breakpoint 7cen t(7;17)7cen |
| Remarks |
Product of conception fibroblast culture; analysis with probe YNZ22 detected a deletion at locus D17S5 (17p13.3) |
| Passage Frozen |
3 |
| Split Ratio |
1:5 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
| Serum |
15% fetal bovine serum Not inactivated |
| Substrate |
None specified |
| Subcultivation Method |
trypsin-EDTA |
| Supplement |
- |
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