GM23886
LCL from B-Lymphocyte
Description:
HEMOGLOBIN F, HEREDITARY PERSISTENCE OF
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases Chromosome Abnormalities |
Biopsy Source
|
Peripheral vein
|
Cell Type
|
B-Lymphocyte
|
Tissue Type
|
Blood
|
Transformant
|
Epstein-Barr Virus
|
Sample Source
|
LCL from B-Lymphocyte
|
Family Member
|
3
|
Family History
|
N
|
Relation to Proband
|
brother
|
ISCN
|
46,XY.arr 1p31.3(63571339-63844510)x3
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by LINE assay |
|
Remarks |
Brother of affected individual (GM23883); mother (GM23885), and sister (GM23884) also in the repository. |
Split Ratio |
1:2 |
Temperature |
37 C |
Percent CO2 |
5% |
Percent O2 |
AMBIENT |
Medium |
Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent |
Serum |
30% fetal bovine serum Not Inactivated |
Substrate |
None specified |
Supplement |
- |
|
|