GM24218
Fibroblast from Skin, Skin
Description:
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
LAMININ, ALPHA-2; LAMA2
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Repository
|
NIGMS Human Genetic Cell Repository
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| Subcollection |
Heritable Diseases
Muscular Dystrophies
CMD Specific |
| Class |
Congenital Muscle Diseases |
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Biopsy Source
|
Skin
|
|
Cell Type
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Fibroblast
|
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Tissue Type
|
Skin
|
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Transformant
|
Untransformed
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Sample Source
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Fibroblast from Skin, Skin
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|
Race
|
Asian, Other
|
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Ethnicity
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Not Hispanic/Latino
|
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Country of Origin
|
USA
|
|
Family Member
|
1
|
|
Family History
|
Y
|
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Relation to Proband
|
proband
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Species
|
Homo sapiens
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|
Common Name
|
Human
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Remarks
|
|
| PDL at Freeze |
5.69 |
| Passage Frozen |
3 |
| |
| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by LINE assay |
| |
| Remarks |
Clinically affected; brain involvement; maximum motor function ever achieved and still maintained: walks without assistance outdoors; uses respiratory support only when ill; same as GM24241 (LCL). |
| Cumulative PDL at Freeze |
5.69 |
| Passage Frozen |
3 |
| Split Ratio |
1:2 |
| Temperature |
37 C |
| Percent CO2 |
5% |
| Percent O2 |
AMBIENT |
| 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 |
| Supplement |
- |
|