HT-2 Clone A5E; Spleen; Mouse (Mus Musculus) Item ID
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- General Information
- Characteristics
- Quality Control Specifications
- History
| Permits and Restrictions | View Permits |
|---|---|
| Organism | Mus musculus, mouse |
| Tissue | spleen |
| Cell Type | IL-2 dependent T lymphocyte |
| 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. |
| Strain | BALB/c |
| Applications | The line is dependent on IL-2 for growth and can be used to measure IL-2 activity in a very rapid and sensitive assay. The cells are commonly used for characterization of lymphokines and cytokines. |
| Derivation | The HT-2 cell line was derived in 1979 by J. Watson at the University of Auckland from a culture of BALB/c spleen cells activated by sheep erythrocytes in the presence of IL-2. |
|---|---|
| Antigen Expression | Thy-1 |
| Receptor Expression | interleukin 2 (IL-2) |
| Comments | The A5E clone was selected to provide a homogeneous population that is highly sensitive to IL-2. In addition to IL-2, substantial proliferation is seen in the presence of interleukin 4 (interleukin-4, IL-4, also known as BSF-1). |
| Complete Growth Medium | The complete medium for culturing CRL-1841 is composed of: 399.5 mL RPMI-1640 (ATCC 30-2001) 50 mL FBS (ATCC 30-2020) 0.5 mL 2-Mercaptoethanol (Gibco 21985-023) 50 mL Rat T-STIM with Con A (Thermo Fisher CB-40115) |
|---|---|
| Subculturing | Cultures can be maintained by addition or replacement of fresh medium. Subcuture every two days at 3.5 x 10 4 viable cells/mL. Medium Renewal: Every 2 to 3 days |
| Cryopreservation | Freeze medium: complete growth medium, 95%; DMSO, 5% |
| Culture Conditions | Temperature: 37°C |
| Name of Depositor | JF Weaver, A Creasey |
|---|---|
| Year of Origin | 1979 |
| References | Kupper T, et al. Growth of an interleukin-2/interleukin 4-dependent T cell line induced by granulocyte-macrophage colony-stimulating factor (GM-CSF). J. Immunol. 138: 4288-4292, 1987. PubMed: 2953804 Ho SN, et al. Differential bioassay of interleukin-2 and interleukin-4. J. Immunol. Methods 98: 99-104, 1987. PubMed: 3494085 Lee F, et al. Isolation and characterization of a mouse interleukin cDNa clone that expresses B-cell stimulatory factor 1 activities and T-cell and mast-cell-stimulating activities. Proc. Natl. Acad. Sci. USA 83: 2061-2065, 1986. PubMed: 3083412 Watson J. Continuous proliferation of murine antigen-specific helper T lymphocytes in culture. J. Exp. Med. 150: 1510-1519, 1979. PubMed: 92524 . . J. Biol. Response Modif. 4: 96-109, 1985. Kupper T, et al. Autocrine growth of T cells independent of interleukin 2: identification of interleukin 4 (IL 4, BSF-1) as an autocrine growth factor for a cloned antigen-specific helper T cell. J. Immunol. 138: 4280-4287, 1987. PubMed: 2953803 Woods A, et al. Granulocyte-macrophage colony stimulating factor produced by cloned L3T4a+, class II-restricted T cells induces HT-2 cells to proliferate. J. Immunol. 138: 4293-4297, 1987. PubMed: 2953805 Kotanides H, Reich NC. Interleukin-4-induced STAT6 recognizes and activates a target site in the promoter of the interleukin-4 receptor gene. J. Biol. Chem. 271: 25555-25561, 1996. PubMed: 8810328 |
E: [email protected]: 1300 552 003
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