OCI-AML3 Cells
USD$375.00*
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).
General information
| Description | OCI-AML3 is a human acute myeloid leukemia (AML) cell line derived from a patient with acute myelomonocytic leukemia (FAB classification M4). This cell line is extensively used in leukemia research due to its well-characterized genetic profile and relevance to studying AML pathogenesis and therapeutic response. OCI-AML3 cells are particularly notable for harboring a heterozygous mutation in the nucleophosmin (NPM1) gene, a common alteration in AML that is associated with abnormal localization of the NPM1 protein to the cytoplasm, as well as a DNMT3A R882C mutation, which is implicated in epigenetic dysregulation. These features make OCI-AML3 a highly relevant model for studying key molecular mechanisms in AML. OCI-AML3 cells grow in suspension and exhibit characteristics of immature myeloid cells with monoblast-like morphology. The cell line has been widely used to study apoptosis, proliferation, and differentiation pathways in AML, as well as the molecular consequences of NPM1 and DNMT3A mutations. It is also a valuable model for investigating the role of epigenetic regulation in leukemogenesis, as DNMT3A mutations are known to contribute to global changes in DNA methylation patterns. OCI-AML3 is a preferred model for preclinical drug development and screening, particularly for evaluating epigenetic modulators such as DNA methyltransferase inhibitors and histone deacetylase inhibitors, as well as small-molecule inhibitors targeting signaling pathways and anti-apoptotic proteins. This cell line is also utilized in studies examining mechanisms of drug resistance and the development of combination therapy strategies. Overall, OCI-AML3 remains a critical tool for advancing the understanding of AML biology and for identifying novel therapeutic approaches for this aggressive hematologic malignancy. |
|---|---|
| Organism | Human |
| Tissue | Peripheral blood |
| Disease | acute myeloid leukemia |
| Synonyms | OCI-Aml-3, OCI/AML-3, OCI-AML3, OCI/AML3, OCI AML3, OCIAML3, Ontario Cancer Institute-Acute Myeloid Leukemia-3 |
Characteristics
| Age | 57 years |
|---|---|
| Gender | Male |
| Ethnicity | Caucasian |
| Morphology | Epithelial-like |
| Growth properties | Suspension |
Regulatory Data
| Citation | OCI-AML3 (Cytion catalog number 305432) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_1844 |
Biomolecular Data
| Viruses | EBV -, HBV -, HCV -, HIV-1 -, HIV-2 -, HTLV-1/2 -, MLV -, SMRV - |
|---|---|
| Mutational profile | Mutation: 2978, DNMT3A, p.Arg882Cys (c.2644C>T), Heterozygous; Mutation: NRAS, p.Gln61Leu (c.182A>T), Homozygous; Mutation: NPM1, p.Trp288Cysfs*12 (c.860_863dupTCTG), Heterozygous |
| Karyotype | Hyperdiploid karyotype - 48(45-50)<2n>X/XY, +1, +5, +8, der(1)t(1;18)(p11;q11), i(5p), del(13)(q13q21), dup(17)(q21q25) - sideline with r(Y)x1-2 - hemizygous for RB1 |
Handling
| Culture Medium | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
|---|---|
| Supplements | Supplement the medium with 20% FBS |
| Doubling time | 30-40 hours |
| Seeding density | 2 to 5 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 |
|
| 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. |
|---|
Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 305432-260126 | Certificate of Analysis | 02. Mar. 2026 | 305432 |