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Daudi Cell Line

General Information
OrganismHomo sapiens, human
Cell Line DescriptionThe Daudi cell line was established in 1967 from a 16-year-old African boy diagnosed with Burkitt's lymphoma, a type of lymphoma. Named after the patient from whom it was derived, the Daudi cell line is characterized by Epstein-Barr virus (EBV) positivity, a common feature of Burkitt's lymphoma and several other lymphoproliferative disorders. EBV infection in these cells provides a unique model for studying the role of the virus in tumorigenesis, particularly in B-cell malignancies. A notable feature of the DAUDI cell line is the presence of c-Myc translocations, specifically the t(8;14)(q24;q32) translocation. This translocation results in constitutive upregulation of the MYC gene, which results in overexpression of β-catenin. Dysregulation of the β-catenin signaling pathway has been implicated in the induction of stemness in cancer cells. Therefore, the DAUDI cell line provides an opportunity to study the molecular mechanisms underlying the development and progression of Burkitt's lymphoma, particularly the role of c-Myc and β-catenin in promoting stemness and tumorigenic potential.
DiseaseBurkitts lymphoma
MorphologyLymphoblast
GenderMale
Age16 years
Product FormatFrozen
Growth ModeSuspension
Biosafety Level2
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Applications1. Cancer Research
2. Immunology Studies
3. Vaccine Development
4. Drug Screening
5. Virology Research
Shipped InDry ice
Storage Temperature−196°C
Additional InfoDaudi human cells lack expression of classical major histocompatibility complex (MHC) class I molecules on their surface due to the absence of β-2-microglobulin, a key component responsible for the correct intracellular folding and processing of MHC class I molecules in the endoplasmic reticulum. The lack of β-2-microglobulin in the Daudi cell line results in a lack of glycosyl modifications necessary for the proper expression of these molecules on the cell surface.
Characteristics
Karyotype46, almost diploid
TumorigenicYes, in nude mice
Antigen ExpressionCD10+, CD19+, CD20+, CD21+, CD22+, CD23-, CD24-, CD32+, CD37+, CD38+, CD39-,CD40+, CD54+, CD72+, CD73-, CD75+, CD77+, CD81+, CD82+, CD83-, CD84+, CD86+
Expression MarkersComplement, expressed; Fc, expressed
Mycoplasma TestNegative
Culture Conditions and Handling
SubculturingThe culture can be maintained by adding fresh medium or replacing the medium. Alternatively, the culture can be established by centrifugation and subsequently resuspended at a density of 3 to 5 x 105 viable cells/mL. Maintain cell density between 3 x 105 and 2 to 3 x 106 viable cells/mL. T-75 flasks are recommended for subculturing this product.
Medium RenewalAdd fresh medium every 2 to 3 days.
Culture MediumRPMI 1640 + 2mM Glutamine + 10% Foetal Bovine Serum (FBS).
Culture ConditionsAtmosphere: Air, 95%; CO2, 5%; Temperature: 37℃
CryopreservationComplete growth medium supplemented with 5% (v/v) DMSO

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* For research use only. Not intended for any clinical use.
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