GM01584
Amniotic fluid-derived cell line from Amniotic fluid
Description:
MUCOPOLYSACCHARIDOSIS TYPE II
|
Repository
|
NIGMS Human Genetic Cell Repository
|
| Subcollection |
Heritable Diseases
Lysosomal Storage Diseases |
|
Biopsy Source
|
Amniotic fluid
|
|
Cell Type
|
Amniotic fluid-derived cell line
|
|
Transformant
|
Untransformed
|
|
Sample Source
|
Amniotic fluid-derived cell line from Amniotic fluid
|
|
Race
|
White
|
|
Family Member
|
2
|
|
Relation to Proband
|
brother
|
|
Confirmation
|
Clinical summary/Case history
|
|
Species
|
Homo sapiens
|
|
Common Name
|
Human
|
|
Remarks
|
|
| Passage Frozen |
6 |
| |
| iduronate-2-sulfatase |
According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 3.1.6.13 |
| |
| Remarks |
46,XY; deficient iduronate sulfatase; Israeli; affected brother is GM01583 Fibroblast |
| Passage Frozen |
6 |
| Split Ratio |
1:3 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| Medium |
Amniotic Fluid Culture Medium |
| Serum |
none Not inactivated |
| Substrate |
None specified |
| Subcultivation Method |
trypsin-EDTA |
| Supplement |
- |
|
|