AG08541
Fibroblast from Skin, Arm
Description:
ALZHEIMER DISEASE; AD
Repository
|
NIA Aging Cell Culture Repository
|
Subcollection |
German Alzheimer Disease |
Biopsy Source
|
Arm
|
Cell Type
|
Fibroblast
|
Tissue Type
|
Skin
|
Transformant
|
Untransformed
|
Sample Source
|
Fibroblast from Skin, Arm
|
Race
|
White
|
Ethnicity
|
GERMAN
|
Family Member
|
13
|
Relation to Proband
|
V-19
|
Confirmation
|
Clinical summary/Case history
|
ISCN
|
46,XX/46,XX,t(1;21)(q21;p12),t(11;17) (p15.5;q11.2)/45,X
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
PDL at Freeze |
14 |
Passage Frozen |
7 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis |
|
Remarks |
The donor has had progressive impairment of memory attended by increasing difficulty in performing household chores. She has visuospatial disorientation and difficulty with expressive speech. Neurological exam revealed disorientation, problems following commands, and regressive reflexes. She also exhibited a decrease in associated movements, slight cogwheel rigidity, and bradykinesia. This patient also has almost continuous myoclonus. The skin biopsy was taken ante-mortem from the forearm. Culture was initiated on 12/10/85 using explants of minced skin. The cell morphology is fibroblast-like. The culture is a mosaic with karyotype: 46,XX/46,XX,t(1;21)(q21;p12),t(11;17)(p15.5;q11.2)/45,X; unbalanced; 82%/8%/6% with 4% random chromosomal abnormalities. Culture was frozen at PDL 14. The legacy karyotype description shown in this Remark may not be representative of the current available product. |
Frommelt P, Schnabel R, Kuhne W, Nee LE, Polinsky RJ, Familial Alzheimer disease: a large, multigeneration German kindred. Alzheimer Dis Assoc Disord5:36-43 1991 |
PubMed ID: 2025423 |
|
St George-Hyslop PH, Tanzi RE, Polinsky RJ, Haines JL, Nee L, Watkins PC, Myers RH, Feldman RG, Pollen D, Drachman D, et al, The genetic defect causing familial Alzheimer's disease maps on chromosome 21. Science235:885-90 1987 |
PubMed ID: 2880399 |
Cumulative PDL at Freeze |
14 |
Passage Frozen |
7 |
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 |
- |
|
|