GM10613
Fibroblast from Fetal, Unspecified
Description:
TRANSLOCATED CHROMOSOME
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Chromosome Abnormalities |
Biopsy Source
|
Unspecified
|
Cell Type
|
Fibroblast
|
Tissue Type
|
Fetal
|
Transformant
|
Untransformed
|
Sample Source
|
Fibroblast from Fetal, Unspecified
|
Relation to Proband
|
proband
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
ISCN
|
46,XX,t(20;21)(20pter>20q11.2:: 21p11.2>21pter;21qter>21p11.2:: 20q11.2>20qter)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
4 |
|
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 |
|
Cytogenetics |
Chromosome 20: TRANSLOCATION Breakpoint 20q11 t(20;21)20q11 |
|
Chromosome 21: TRANSLOCATION Breakpoint 21p11 t(20;21)21p11 |
Remarks |
First trimester spontaneous abortion; in situ hybridization with probe D2021 for chromosome #20 centromere utilized to confirm breakpoints; slow growing culture |
Passage Frozen |
4 |
Split Ratio |
1:2 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Eagle's MEM with Hank's BSS, with 26mM Hepes; ambient CO2 with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not inactivated |
Substrate |
None specified |
Subcultivation Method |
trypsin-EDTA |
Supplement |
- |
|
|