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Amyloid A, Serum, Human (Serum, Amyloid A, SAA) BioAssay(TM) ELISA Kit

Cat no: A2275-60C


Supplier: United States Biological
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Amyloid A, Serum, Human (Serum, Amyloid A, SAA) BioAssay(TM) ELISA Kit is to be used for the in vitro quantitative determination human serum amyloid A (SAA) concentrations in serum, plasma, cell culture supernatant and other biological fluids. Amyloidosis includes a family of diseases which have in common the extracellular deposition of beta-pleated ?brillar protein. Amyloidosis associated with chronic in?ammatory conditions. (AA-type) and Amyloidosis related to plasma cel dyscrasia (AL-type) are the most common. The frequency of amyloidosis associated with chronic hemodialysis (B2M-type) is growing rapidly. Sensitivity: Calibrator Diluent 1: 1.1ng/ml Calibrator Diluent 2: 0.6ng/ml Range: 0-80ng/ml Specificity: Recognizes both natural and recombinant human SAA. Does no exhibit detectable crossreactivity with human IL-8, IL-1b, MCAF, FGF, TGF-b, EGF, GM-CSF, M-CSF, MCP-3, TNF-a, RANTES and EPO. Kit Components: A2275-60C1: SAA microtiter plate, 1 x 96wells A2275-60C2: SAA conjugate, 1 x 15ml A2275-60C3: SAA standard, 2 x 160ng A2275-60C4: Calibator Diluent I, 1 x 30ml A2275-60C5: Calibator Diluent II, 1 x 30ml A2275-60C6: Wash buffer (20X), 1 x 60ml A2275-60C7: Substrate A, 1 x 11ml A2275-60C8: Substrate B, 1 x 11ml A2275-60C9: Stop solution, H2SO4, 1 x 14ml Storage and Stability: Store *A2275-60C3 at -20 degrees C. Store other components at 4 degrees C. Stable for 6 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Catalogue number: A2275-60C
Applications: ELISA
Size: 96Tests
References: US Biological application references: 1. Viguerie, N. et al., (2012) Physiol. Genomics physiolgenomics.00032.2011 2. Hergenroeder, G. et al., (2008) J. Neurotrauma 25:79-93. 1. Skinner, M., J. Internal Med. 232: 514-523 (1992). 2. Kisilevsky, R., Med. Hypoth. 35(3): 37-41 (1991). 3. Malle, E., et al., Atheroscl. 102: 131-146 (1993). 4. Baussermann, L.L., et al. Eur. J. Clin. Invest. 18: 619-626, (1988). 5. Badolato, R., et al., J. Exp. Med. 180: 203-209 (1994). 6. Xu, L., et al., J. Immunol. 155: 1184-1190 (1995). 7. Liang, J., et al., J. Lipid Res. 36: 37-46 (1995). 8. Knecth, A., et al., Ann. Int. Med. 102(1): 71-72 (1985). 9. Reinoff, J.R., et al., Mol. Bio. Med. 7: 287-298 (1990). 10. Marhaug, G., et al., Acta. Peadiatr. Scand. 72: 861-866(1983). 11. Casl, M.T., et al., Nephron. 70: 112-113 (1995). 12. Casl, M.T., et al., Ann. Clin. Biochem. 30: 272-277 (1993). 13. Husebekk, A., et al., Scand. J. Infec. Dis. 18: 389-394 (1986). 14. Nakayama, T., et al., Clin. Chem. 39(2): 293-297 (1993). 15. Honkanen, E., et al., Nephron. 57: 283-287 (1991). 16. Hiroyuki, M., et al., Arch. Dis. Child. 68: 210-214 (1993). 17. Thomson, D., et al., Ann. Clin. Biochem. 29: 123-131 (1992). 18. Luizzo, G., et al., N. Eng. J. Med. 331: 417-424 (1994). 19. Casl, M.T., et al., Ann. Clin. Biochem. 32: 196-200 (1995).

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