CL-0498
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Product Introduction
| Cell Name | MEG-01 |
| Synonyms | Meg-01;MEG01;Meg01 |
| Cellosaurus Accession | CVCL_0425 |
| Organism | Human |
| Growth Properties | Semi-adherent and semi-suspension |
| Morphology | Lymphoblast-like |
| Disease | leukemia cells |
| Tissue | Bone marrow |
| Age | 55Y |
| Sex | Male |
| Instructions | 1. Check all containers for leakage or breakage. 2. Remove the frozen cells from the dry ice packaging and immediately transfer them to liquid nitrogen (liquid or vapor phase) for long-term cryopreservation. |
| Complete Medium | RPMI-1640 [PM150110]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:2-1:3 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 1-2 min |
| Subculturing Procedure | 1. This cell line displays mixed adherent and suspended phenotypes. Suspended cells remain viable. Transfer the single-cell suspension into a centrifuge tube and pellet the cells via centrifugation at 1200 × g (approximately 250 × g). 2. Weakly adherent cells can be dispersed by gentle pipetting to form a homogeneous single-cell suspension. 3. For firmly adherent cells, rinse with PBS, then add 1–2 mL of 0.25% Trypsin-EDTA to the culture flask. Incubate at 37°C. Once the cells round up and detach from the vessel surface, add 4–6 mL of complete medium to terminate digestion. Gently pipette to generate a single-cell suspension, then harvest cells by centrifugation. 4. Mix all harvested suspended and adherent cell populations, then seed the cells into fresh culture vessels at the recommended split ratio. |
| Freeze Medium | General Freezing Medium [PB180436] |
| Storage Conditions | For long-term cryopreservation, cryovials should be stored in liquid nitrogen at −150°C to −196°C. Storage at −80°C is restricted to short-term interim use only. |
| Background | MEG-01 cells were derived from the bone marrow of a patient with chronic myeloid leukemia (CML) in megakaryoblastic crisis. The cells are positive for cytoplasmic factor VIII, surface glycoprotein IIb/IIIa, periodic acid–Schiff (PAS) activity, α-naphthyl acetate esterase, and acid phosphatase, but negative for myeloperoxidase, α-naphthyl butyrate esterase, naphthol AS-D chloroacetate esterase, and alkaline phosphatase. They stain positively with the monoclonal antibodies BA-1 (anti-B cell/granulocyte), HPL-3 (anti-glycoprotein IIb/IIIa), and 20.3 (anti-monocyte/platelet), and are negative for other lymphoid and myeloid lineage markers. |
Documents
Publications
Journal: Frontiers in Nutrition (2026) IF: 5.1
DOI: 10.3389/fnut.2026.1815132
Product Cited: MEG-01 Cells Line
Journal: JOURNAL OF TRACE ELEMENTS IN MEDICINE AND BIOLOGY (2026) IF: 3.3
DOI: 10.1016/j.jtemb.2026.127854
Product Cited: MEG-01 Cells Line
Journal: CELLULAR & MOLECULAR BIOLOGY LETTERS (2025) IF: 10.2
DOI: 10.1186/s11658-025-00759-x
Product Cited: MEG-01 Cells Line
Journal: BRITISH JOURNAL OF HAEMATOLOGY (2025) IF: 5.1
DOI: 10.1111/bjh.20006
Product Cited: MEG-01 Cells Line
Journal: CANCER IMMUNOLOGY IMMUNOTHERAPY (2025) IF: 5.1
DOI: 10.1007/s00262-025-04257-z
Product Cited: Penicillin-Streptomycin-Amphotericin B Solution, 100 ×, M-07e Cells Line, DMEM (High glucose) Complete Medium (10), Human Peripheral Blood Monocyte Complete Medium, MEG-01 Cells Line, Human Peripheral Blood Monocytes, DMEM (High glucose) Complete Medium (20), GM-CSF/CSF2/CSF, Human, Recombinant
