KU812 Cells
CAD$545.10*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
General information
| Description | The KU812 cell line is a human leukemic cell line originally derived from a patient with chronic myelogenous leukemia (CML) in the blastic crisis phase. It is notable for its capacity to differentiate into basophilic and erythroid lineages under specific conditions, making it a valuable tool for studying hematopoietic differentiation and related malignancies. The cell line exhibits characteristics of basophilic precursors, including the presence of metachromatic granules that are positive for toluidine blue and astra blue staining, and it synthesizes histamine, indicative of basophilic activity. KU812 cells are particularly relevant in investigating complement activation-related pseudoallergy (CARPA) and hypersensitivity reactions mediated by basophils. This utility stems from their robust response to complement proteins like C3a and C5a, which trigger the release of histamine and other inflammatory mediators, mimicking pseudoallergic reactions. KU812 cells express cell-surface markers such as CD63 and CD203c, which are associated with basophilic activation and degranulation. These markers have been employed in flow cytometry-based protocols to evaluate the immunological compatibility of nanomedicines and other biologics. Additionally, KU812 cells demonstrate erythroid differentiation potential when cultured in erythropoietin-supplemented conditions. This includes spontaneous maturation into erythroid cells capable of synthesizing various hemoglobins, such as adult and fetal forms. These features underline their utility in studying erythropoiesis alongside basophilic differentiation, making KU812 a versatile model for hematological research. |
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| Organism | Human |
| Tissue | Peripheral blood |
| Disease | Chronic myelogenous leukemia, BCR-ABL1 positive |
| Synonyms | Ku812, KU-812, KU.812, KU 812 |
Characteristics
| Age | 38 years |
|---|---|
| Gender | Male |
| Ethnicity | Japanese |
| Morphology | Lymphoblast-like |
| Cell type | Basophil progenitor cell |
| Growth properties | Suspension |
Regulatory Data
| Citation | KU812 (Cytion catalog number 305306) |
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| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_0379 |
Biomolecular Data
| Antigen expression | CD3, ANPEP (CD13) |
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| Mutational profile | Mutation: TP53, p.Lys132Arg (c.395A>G), homozygous; Gene fusion: BCR-ABL, BCR exon 14 fused to ABL1 exon 2 (b3a2 transcript) |
| Karyotype | The cells contain at least one Ph1 (Philadelphia) chromosome. |
Handling
| Culture Medium | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
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| Supplements | Supplement the medium with 10% FBS, add 2.5 g/L glucose and 10 mM HEPES |
| Subculturing | Gather the suspension cells in a 15 ml tube and gently wash the adherent cells with PBS lacking calcium and magnesium (use 3-5 ml for T25 flasks and 5-10 ml for T75 flasks). Apply Accutase (1-2 ml for T25 flasks, 2.5 ml for T75 flasks) ensuring full coverage of the cell layer. Allow the cells to incubate at room temperature for 10 minutes. Following incubation, combine and centrifuge both the suspension and adherent cells. After centrifugation, carefully resuspend the cell pellet and transfer the cell suspension into new flasks containing fresh medium. |
| Seeding density | 3 x 105 cells/mL |
| Fluid renewal | 2 to 3 times per week |
| Freeze medium | As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress. |
| Thawing and Culturing Cells |
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| Incubation Atmosphere | 37°C, 5% CO2, humidified atmosphere. |
| Shipping Conditions | Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage. |
| Storage Conditions | For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen. |
Quality Control & Molecular Analysis
| Sterility | Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. |
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