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REH Cell Line

General Information
OrganismHomo sapiens, human
Cell Line DescriptionREH, established in 1974 as the first B cell precursor acute lymphoblastic leukemia (ALL) cell line, was derived from the peripheral blood of a 15 year-old female patient at relapse. REH has a near-diploid karyotype characterized by complex structural rearrangements, including several interchromosomal translocations. Among the features described in this cell line is a complex four-way translocation t(4;12;21;16) that results in the canonical subtype-defining ETV6-RUNX1 fusion gene and glucocorticoid (GC) resistance attributed to lack of a GC receptor. These REH cells are often used in research on immune system disorders and cancer.
TissuePeripheral blood
DiseaseAcute lymphoblastic leukemia (ALL)
MorphologyLymphoblast
Age15 years
GenderFemale
Product FormatFrozen
Growth ModeSuspension
Biosafety Level1
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. Drug Development Research
3. Genetic Studies
4. Immunotherapy Research
5. Biomarker Discovery
6. Toxicity Testing
Shipped InDry ice
Storage Temperature−196°C
Additional InfoThe REH cell line comes from a relapsed patient, making it particularly notable that several deletions identified in the study, affecting genes TBL1XR1 (146k deletion on 3q26.32), NR3C1 (205 kbp deletion on 5q31.3) and BTG1 (260kbp deletion on 12q21.33), have been shown to contribute to its GC drug resistance.
Characteristics
Antigen ExpressionCD3 A (17%) B (17%) C (20%), CD4 (15%), CD10 (55%)
Mycoplasma TestNegative
Culture Conditions and Handling
SubculturingMaintain the culture by regularly adding or replacing the medium. Start the culture at 2 x 10^5 cells/mL and maintain the cell concentration in the range of 1 x 10^5 to 1 x 10^6 cells/mL for optimal growth.
Medium Renewal2 to 3 times per week
Subcultivation RatioThe ratio of 1:2 to 1:4 is recommended.
Culture MediumRPMI 1640, w: 2.1 mM stable Glutamine, w: 2.0 g/L NaHCO3. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Culture ConditionsAtmosphere: Air, 95%; CO2, 5%; Temperature: 37℃
CryopreservationFetal bovine serum supplemented with 5% (v/v) DMSO

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