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Tumor Necrosis Factor alpha, Human (TNFa) BioAssay(TM) ELISA Kit

Cat no: T9160-01

Tumor Necrosis Factor alpha, Human (TNFa) BioAssay(TM) ELISA Kit

Tumor Necrosis Factor alpha (TNF-a), also known as cachectin was initially named for its remarkable ability to cause hemorrhagic necrosis of tumors in mice. The TNF-a gene located on chromosome 6 encodes a 233aa prohormone bound to the plasma membrane, with the mature form (157aa, 17kD) exposed on the extracellular surface. Soluable, mature TNF-a is released upon cleavage of the C-terminal. The primary source in vivo of TNF-a is thought to be the monocyte/macrophage but various cell types are known to express this cytokine such as lymphocytes, basophils, eosinophils, mast cells, NK cells, T cells, B cells, kerantinocytes, Kupffer cells, astrocytes, and some types of tumors. TNF-a is produced upon stimulation with cytokines such as IL-1, 1L-2, GM-CSF, TNF-a itself and with bacterial lipopolysaccharide (LPS) which is a potent inducer. TNF-a once produced and secreted will bind to TNF-a pleiotropic cytokine that can induce disease through TNF-a toxicity (tissue injury, catabolic illness, and mediating shock) and improve host defence mechanisms (stimulating inflammation and increasing immune cell function). In the future, therapies may be developed by blocking TNF-a harmful effects and enhancing TNF-a beneficial effects.\n\nThis TNF-a enzyme linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific to TNF-a. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for TNF-a and incubated. TNF-a if present, will bind and become immobilized by the antibody pre-coated on the wells and then be "sandwiched" by biotin conjugate. In order to measure the concentration of TNF-a in the samples, this kit includes two calibration diluents (Calibrator Diluent I for serum/plasma testing and Calibrator Diluent II for cell culture supernatant testing.) According to the testing system, the provided standard is diluted (2-fold) with the appropriate Calibrator Diluent and assayed at the same time as the samples. This allows the operator to produce a standard curve of Optical Density (O.D) versus TNF-a concentration (pg/ml). The concentration of TNF-a in the samples is then determined by comparing the O.D. of the samples to the standard curve.\n\nSensitivity: \nCalibrator Diluent I: 2.4pg/ml\nCalibrator Diluent II: 2.4pg/ml\n\nRange:\n15.625-1000pg/ml\n\nKit Components:\nT9160-01A: TNFa Microtiter plate, 1x96 wells \nT9160-01B: Pab (Biotin) 1x 7ml \nT9160-01C: Avidin (HRP) 1x12ml \nT9160-01D: TNF-a Standard, 2x1vial\nT9160-01E: Calibrator Diluent I, 1x22ml\nT9160-01F: Calibrator Diluent II ,1x22ml \nT9160-01G: Wash Buffer, 20X 1x60ml \nT9160-01H: Substrate, A 1x11ml \nT9160-0J: Substrate B, 1x11ml\n1T9160-01K: Stop Solution, 1x14ml 2N Sulphuric Acid (H2SO4). \n\nStorage and Stability:\nStore kit components at 4 degrees C except *T9160-01D. Stable for 6 months. Store T9160-01D lyophilized powder at 4 degrees C. Store reconstituted stock at -20 degrees C for <30 days. For maximum recovery of product, centrifuge the original vial prior to removing the cap. Further dilutions can be made in assay buffer.

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SPECIFICATIONS

Catalog Number

T9160-01

Size

96Tests

Applications

ELISA

References

1. Carswell, E.A. et al. (1975) Proc. Natl. Acad. Sci., 72: 3666. 2. Kriegler, M. et al. (1988) Cell. 53:45. 3. Jue, D.M. et al. (1990) Biochem. 29: 8371.4. Thomson, A. (1994) In The Cytokine Handbook (eds K.J. Tracey), Academic Press Limited, London, pp.290-300. 5. Hohmann, H.P. et al. (1989) J Biol. Chem. 264: 14927. 6. Pfeffer, K. et al. (1993) Cell. 73: 457. 7. Tartaglia, L.A. et al. (1993) Cell. 73: 213. 8. Tartaglia, L.A. et al. (1991) Proc. Natl. Acad. Sci. USA 88:3535. 9. Tracey, K.J. et al. (1987) Nature 330:662. 10. Waage, A. et al.(1987) Lancet. 1:355. 11. Pujol-Borrell, R. et al. (1987) Nature 326:304. 12. Mozes, T. et al. (1991) Immunol Lett. 27: 157.

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