KU812 Cells
USUSD$395.00*
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).
一般資訊
| 說明 | 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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| 生物體 | Human |
| 組織 | Peripheral blood |
| 疾病 | Chronic myelogenous leukemia, BCR-ABL1 positive |
| 同義詞 | Ku812, KU-812, KU.812, KU 812 |
特徵
| 年齡 | 38 years |
|---|---|
| 性別 | Male |
| 族裔 | Japanese |
| 形態學 | Lymphoblast-like |
| 細胞類型 | Basophil progenitor cell |
| 生長特性 | Suspension |
監管數據
| 引用 | KU812 (Cytion catalog number 305306) |
|---|---|
| 生物安全等級 | 1 |
| NCBI_TaxID | 9606 |
| Cellosaurus 編號 | CVCL_0379 |
生物分子資料
| 抗原表達 | CD3, ANPEP (CD13) |
|---|---|
| 突變譜 | Mutation: TP53, p.Lys132Arg (c.395A>G), homozygous; Gene fusion: BCR-ABL, BCR exon 14 fused to ABL1 exon 2 (b3a2 transcript) |
| 核型分析 | The cells contain at least one Ph1 (Philadelphia) chromosome. |
處理方式
| 培養基 | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
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| 營養補充品 | Supplement the medium with 10% FBS, add 2.5 g/L glucose and 10 mM HEPES |
| 傳代培養 | 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. |
| 播種密度 | 3 x 105 cells/mL |
| 流體更新 | 2 to 3 times per week |
| 冷凍培養基 | 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. |
| 細胞解凍與培養 |
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| 培養環境 | 37°C, 5% CO2, humidified atmosphere. |
| 運送條款 | 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. |
| 儲存條件 | 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. |
品質控制與分子分析
| 不孕症 | 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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