GM00304
Fibroblast from Skin, Unspecified
Description:
CYSTINOSIS, NEPHROPATHIC; CTNS
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases Lysosomal Storage Diseases |
Class |
Disorders of Amino Acid Metabolism |
Biopsy Source
|
Unspecified
|
Cell Type
|
Fibroblast
|
Tissue Type
|
Skin
|
Transformant
|
Untransformed
|
Sample Source
|
Fibroblast from Skin, Unspecified
|
Race
|
White
|
Family Member
|
1
|
Relation to Proband
|
proband
|
Confirmation
|
Clinical summary/Case history
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Remarks |
Skin fibroblasts; formerly GM00091; increased intracellular cystine in fibroblasts; same patient as GM00090A |
Schneider JA, Verroust FM, Kroll WA, Garvin AJ, Horger EO 3d, Wong VG, Spear GS, Jacobson C, Pellett OL, Becker FL, Prenatal diagnosis of cystinosis. N Engl J Med290:878-82 1974 |
PubMed ID: 4816962 |
Passage Frozen |
4 |
Split Ratio |
1:3 |
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 |
- |
|
|