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.
Adherent Suspension
Suspension
Suggested Medium
RPMI 1640 + 4mM Glutamine + 200 µg/ml Sodium Pyruvate (NaPy) + 15% Heat Inactivated (HI-FBS).
Quality Control
LB687 Cell Line was tested and found to be free of mycoplasma, bacterial, viruses, and other toxins. All cells were above 95% viability before freezing.
Morphology
Lymphoblastoid
Shippment
LB687 Cell Line will be shipped using dry ice.
Storage
Store the cell lines in liquid nitrogen vapor (less than -130°C)
Warranty
LB687 Cell Line is for research use only
