LB687
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Description
Description: Established by EBV transformation of mononuclear cells from a peripheral blood sample from a 30 year old male patient. The patient was diagnosed with Xeroderma pigmentosum complementation group A, a rare, autosomal recessive disorder with DNA-repair deficiency.
Also Known As:
Species: Human
Tissue: Blood
Growth Properties: Suspension
Morphology: Lymphoblastoid
Growth Medium: RPMI 1640 + 4mM Glutamine + 200 µg/ml Sodium Pyruvate (NaPy) + 15% Heat Inactivated (HI-FBS).
Subculturing Procedure: Maintain cultures between 3-9 x 100,000 cells/ml, dilute every 1-2 days to 3 x 100,000 cells/mls; 5% CO2; 37°C. Cells form floating aggregates.
Release Conditions: No
Depositor: Dr. J. Cole, MRC Cell Mutation Unit, University of Sussex, Falmer, Brighton, East Sussex, BN1 9RR
Originator: Yes
References: None specified by depositor
Hyperlink to ECACC Cell Line Data Sheet: 98062335
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