Description
Established by EBV transformation of mononuclear cells from peripheral blood of a 41 year old male. The patient was shown to be heterozygote for Xeroderma pigmentosum group A, a rare, autosomal recessive disease with DNA repair deficiencies. A cell line established from a child of this patient with XP cell line is available
Adherent Suspension
Suspension
Suggested Medium
RPMI 1640 + 4mM Glutamine + 200 µg/ml Sodium Pyruvate (NaPy) + 15% Heat Inactivated (HI-FBS).
Quality Control
LB707 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
LB707 Cell Line will be shipped using dry ice.
Storage
Store the cell lines in liquid nitrogen vapor (less than -130°C)
Warranty
LB707 Cell Line is for research use only