GM09501

GM09501 LCL from B-Lymphocyte

Description:

TETRALOGY OF FALLOT

Affected:

No

Sex:

Male

Age:

21 YR (At Sampling)

Overview

Repository

NIGMS Human Genetic Cell Repository

Subcollection

Heritable Diseases

Class

Other Disorders of Known Biochemistry

Alternate IDs

GM18037 [TETRALOGY OF FALLOT]

Biopsy Source

Peripheral vein

Cell Type

B-Lymphocyte

Tissue Type

Blood

Transformant

Epstein-Barr Virus

Sample Source

LCL from B-Lymphocyte

Race

White

Family Member

Relation to Proband

father

Confirmation

Clinical summary/Case history

ISCN

46,XY

Species

Homo sapiens

Common Name

Human

Remarks

Clinically unaffected; 46,XY; 8% of cells show random chromosome loss & 4% are tetraploid

Characterizations

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

Phenotypic Data

Remarks

Clinically unaffected; 46,XY; 8% of cells show random chromosome loss & 4% are tetraploid

External Links

dbSNP

dbSNP ID: 17408

NCBI GTR

187500 TETRALOGY OF FALLOT; TOF

OMIM

187500 TETRALOGY OF FALLOT; TOF

Omim Description

TETRALOGY OF FALLOT

Culture Protocols

Split Ratio

1:4

Temperature

37 C

Percent CO2

Medium

Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent

Serum

15% fetal bovine serum Not Inactivated

Substrate

None specified

Subcultivation Method

dilution - add fresh medium

Supplement

Pricing

Commercial/For-profit:

$311.00USD

Academic/Non-profit/Government:

$176.00USD