Description:
CHROMOSOME INSERTION
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Chromosome Abnormalities |
Cell Type
|
Fibroblast
|
Transformant
|
Untransformed
|
Race
|
White
|
Family Member
|
2
|
Relation to Proband
|
father
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
ISCN
|
46,XY,ins(5;1)(5pter>5q15::1q25>1q32:: 5q15>5qter;1pter>1q25::1q32>1qter)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Passage Frozen |
7 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome 1: INSERTION Breakpoint 1q25 ins(5;1)1q25 |
|
Chromosome 1: INSERTION Breakpoint 1q32 ins(5;1)1q32 |
|
Chromosome 5: INSERTION Breakpoint 5q15 ins(5;1)5q15 |
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 |
- |
|
|