GM06092
LCL from B-Lymphocyte
Description:
GALACTOSIALIDOSIS; GSL
|
Repository
|
NIGMS Human Genetic Cell Repository
|
| Subcollection |
Heritable Diseases
Lysosomal Storage Diseases |
| Class |
Disorders of Carbohydrate Metabolism |
|
Biopsy Source
|
Peripheral vein
|
|
Cell Type
|
B-Lymphocyte
|
|
Tissue Type
|
Blood
|
|
Transformant
|
Epstein-Barr Virus
|
|
Sample Source
|
LCL from B-Lymphocyte
|
|
Race
|
White
|
|
Family Member
|
3
|
|
Relation to Proband
|
father
|
|
Confirmation
|
Clinical summary/Case history
|
|
Species
|
Homo sapiens
|
|
Common Name
|
Human
|
|
Remarks
|
|
| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase Isoenzyme Electrophoresis |
| |
| Remarks |
Normal beta-galactosidase & neuraminidase activity; see GM04306 Fibroblast |
| Shimmoto M, Fukuhara Y, Itoh K, Oshima A, Sakuraba H, Suzuki Y, Protective protein gene mutations in galactosialidosis. J Clin Invest91:2393-8 1993 |
| PubMed ID: 8514852 |
| |
| Andria, Infantile neuraminidase and B-galactosidase deficiencies (galactosialidosis) with mild clinical courses. Perspect Inher Metab Dis4:379 (1981):2393-8 1981 |
| PubMed ID: 8514852 |
| Split Ratio |
1:3 |
| 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 |
| Substrate |
None specified |
| Subcultivation Method |
dilution - add fresh medium |
| Supplement |
- |
|