TALL-104細胞
數(shù)量： 大量
年限： 2 years
細胞類型： T**細胞
是否是腫瘤細胞： 0
物種來源： 人
生長狀態(tài)： 懸浮生長
運輸方式： 凍存運輸
ATCC Number： CRL-11386?
相關(guān)**： 白血病
細胞形態(tài)： **樣
Designations: TALL-104
Depositors: Wistar Institute
Biosafety Level: 1
TALL-104細胞Shipped: frozen
Medium & Serum: See Propagation
Growth Properties: suspension
Organism: Homo sapiens
Morphology: lymphoblast
Source: Disease: acute lymphoblastic leukemia
Cell Type: T lymphoblast;
Cellular Products: interferon gamma (IFN gamma); tumor necrosis factor alpha (TNF alpha); granulocyte monocyte colony stimulating factor (GM-CSF)
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Receptors: T cell antigen receptor alpha/beta (TCR), expressed
interleukin 2 (IL-2), expressed
interleukin 2 (IL-2); T cell antigen receptor alpha/beta (TCR)
Antigen Expression: CD2 +; CD3 +; CD7 +; CD8 +; CD56 +; CD4 -; CD16 -
DNA Profile (STR): Amelogenin: X,Y
CSF1PO: 10,11
D13S317: 9,12
D16S539: 12
D5S818: 12,13
TALL-104細胞D7S820: 7,13
THO1: 7,9
TPOX: 8,9
vWA: 14,18
Cytogenetic Analysis: 46, XY; t(11;14)(p13;q11)
Age: 2 years
Gender: male
Comments: The TALL-104 line was established from the peripheral blood of a child in relapse with T-ALL.
The cells are highly cytotoxic and are capable of tumor destruction in vivo and in vitro.
IL-2 is required from optimal growth and long term cultivation, but the cells can be grown for short periods without IL-2 (growth will be slower).
The cells are positive for the alpha/beta TCR and negative for gamma/delta TCR.
Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Iscove's Modified Dulbecco's Medium, Catalog No. ATCC 30-2005. To make the complete growth medium, add the following components to the base medium: 50 to 100 units/ml recombinant human IL-2; 2.5 microgram/ml human albumin; 0.5 microgram/ml D-mannitol; fetal bovine serum to a final concentration of 20%.
Atmosphere: air, 95%; TALL-104細胞carbon dioxide (CO2), 5%
Temperature: 37.0°C
Growth Conditions: Successful growth of this cell line is very dependent upon the quality of IL-2 used in the growth medium. ATCC recommends using the highest quality IL-2 available.
Subculturing: Protocol: Cultures can be maintained by addition or replacement of fresh medium. Start cultures at least 8 X 10(5) cells/ml.
Note: IL-2 rapidly loses its potency in medium, it is important that fresh IL-2 be used.
Interval: Maintain between 4 X 10(5) and 1 X 10(6) cells/ml.
Medium Renewal: Add medium as cell density increases
Preservation: Freeze medium: Complete growth medium supplemented with 50% fetal bovine serum, and 10% DMSO. Freeze at a cell density of at least 15 X 10(6) cells/ml
Storage temperature: liquid nitrogen vapor phase
References: 22047: TALL-104細胞Santoli D, et al. Cytotoxic T-ALL cell lines and uses therefor. US Patent 5,272,082 dated Dec 21 1993
23356: O'Connor R, et al. Growth factor requirements of childhood acute T-lymphoblastic leukemia: correlation between presence of chromosomal abnormalities and ability to grow permanently in vitro. Blood 77: 1534-1545, 1991. PubMed: 1706955
23357: Cesano A, et al. Homing and progression patterns of childhood acute lymphoblastic leukemias in severe combined immunodeficiency mice. Blood 77: 2463-2474, 1991. PubMed: 2039829
