CL-0498
$ 420.00
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1×10^6Cells/Vial×2Vials
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Product Introduction
General information
| 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 |
Handling information
| 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. |
Reference materials
| 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
Arsenic Sulfide Induces Apoptosis in Myelodysplastic Neoplasm Cells Through the Suppression of ABI2
Journal: BIOLOGICAL PROCEDURES ONLINE (2025) IF: 4.3
DOI: 10.1186/s12575-025-00311-3
Product Cited: K-562 Cells Line, MEG-01 Cells Line, HS-5 Cells Line, skm-1 Cells Line
Levels of Talin1 in Platelet-Derived Microvesicles Affect Platelet Activation in Patients with Nonvalvular Atrial Fibrillation
Journal: BIOCHEMICAL GENETICS (2025) IF: 2.1
DOI: 10.1007/s10528-025-11060-z
Product Cited: MEG-01 Cells Line
Autophagy-enabled Protein Degradation: Key to Platelet Activation and ANGII Production in Patients with Type 2 Diabetes Mellitus
Journal: Heliyon (2024) IF: 3.4
DOI: 10.1016/j.heliyon.2024.e36131
Product Cited: MEG-01 Cells Line
