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MV-4-11-Luc cell line荧光稳转细胞株MV-4-11Luc BioVector NTCC质粒载体菌种细胞基因保藏中心

  • 价  格:¥998635
  • 货  号:MV-4-11-Luc cell line荧光稳转细胞株MV-4-11Luc
  • 产  地:北京
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MV-4-11-Luc cell line荧光稳转细胞株MV-4-11Luc BioVector NTCC质粒载体菌种细胞基因保藏中心
MV4–11-luc cells, which exogenously express firefly luciferase, are used in the orthotopic in vivo model.
Organism Homo sapiens, human
Tissue peripheral blood
Cell Type macrophage
Product Format frozen
Morphology lymphoblast
Culture Properties suspension
Biosafety Level 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Disease biphenotypic B myelomonocytic leukemia
Age 10 years
Gender male
Applications
This cell line is a suitable transfection host.
Karyotype 48, XY, t(4;11)(q21;q23), +8, +19
Derivation
The MV4-11 cell line was established by Rovera and associates from the blast cells of a 10-year-old male with biphenotypic B-myelomonocytic leukemia. The growth factor, granulocyte/macrophage colony-stimulating factor (GM-CSF), was required to establish this cell line and growth factors are necessary for its continuous proliferation in chemically defined medium [PubMed: 3496132].
Clinical Data
male
The MV4-11 cell line was established by Rovera and associates from the blast cells of a 10-year-old male with biphenotypic B-myelomonocytic leukemia.
Antigen Expression
CD4; Homo sapiens
CD10; Homo sapiens
CD15, human; Homo sapiens
CD4 (40-96%); CD10 (4-11%); CD15 (96-99%)
Genes Expressed
CD4; Homo sapiens, CD10; Homo sapiens, CD15, human; Homo sapiens, CD4 (40-96%); CD10 (4-11%); CD15 (96-99%)
Comments
This line can be propagated in medium supplemented with 10% FBS without the addition of growth factors. IL-3 can independently support the long-term growth of this cell line, but IL-3 antagonized the proliferation of MV4-11 cells in the presence of GM-CSF when both factors were used at very low concentrations. Granulocyte colony stimulating factor (G-CSF) synergized with GM-CSF in inducing proliferation of MV4-11 cells; G-CSF alone causes a transient stimulation of the cell line.
This line was formerly designated ATCC HTB-189.
Over 96% of these cells are positive by indirect immunofluorescence for the myelomonocytic antigen CD15, 40-96% are positive for the monocytic antigen CD4, and 4-11% are positive for CD10 [PubMed: 3500218].
Complete Growth Medium The base medium for this cell line is ATCC-formulated Iscove's Modified Dulbecco's Medium, Catalog No. 30-2005. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing
Cultures can be maintained by addition or replacement of fresh medium. Start cultures at 2 X 105 cells/mL and maintain between 1 X 105 and 1 X 106 cells/mL. Corning® T-75 flasks (catalog #431464) are recommended for subculturing this product.
Medium Renewal: Every 2 to 3 days
Note: If the cells are maintained in a serum-free medium, it is necessary to add the following: 0.005 mg/mL transferrin, 0.005 mg/mL insulin, and 5 ng/mL GM-CSF.
Cryopreservation
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37°C
STR Profile
Amelogenin: X,Y
CSF1PO: 10,12
D13S317: 13
D16S539: 11,12
D5S818: 11,12
D7S820: 8,9
TH01: 8,9.3
TPOX: 8,11
vWA: 14,15
U.S. Patent Number
5,516,512
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