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A2275-73M β-Amyloid, aa1-40, Human, BioAssay™ ELISA Kit

Specifications
References
Brand
BioAssay™
Kit Type
Sandwich ELISA
Tests
96
Sample Volume
50ul
Sensitivity
<6pg/ml
Detection Method
Colorimetric
Detection Range
7.8-500pg/ml
Sample Matrix
Tissue culture medium, tissue homogenate and cerebrospinal fluid (CSF)
EU Commodity Code
38220000
UN DOT Shipping
UN2796 PGII
Shipping Temp
Blue Ice
Storage Temp
4°C/-70°C

The United States Biological Human beta Amyloid 1-40 (Hu A beta40) ELISA kit is a solid phase sandwich Enzyme Linked-Immuno-Sorbent Assay (ELISA). A monoclonal antibody specific for the NH2-terminus of Hu b-amyloid has been coated onto the wells of the microtiter strips provided. During the first incubation, standards of known Hu b-amyloid 40 content, controls, and unknown samples are pipetted into the wells and co-incubated with a rabbit antibody specific for the COOH-terminus of the 1-40 b-amyloid sequence. This COOH- terminal sequence is created upon cleavage of the analyzed precursor. Bound rabbit antibody is detected by the use of a horseradish peroxidase-labeled anti-rabbit antibody. After washing, horseradish peroxidase-labeled anti-rabbit antibody (enzyme) is added. After a second incubation and washing to remove all the unbound enzyme, a substrate solution is added, which is acted upon by the bound enzyme to produce color. The intensity of this colored product is directly proportional to the concentration of Hu A beta40 present in the original specimen.

Sensitivity
<6pg/ml
Range
7.8-500pg/ml
Kit Components
*A2275-73M1: beta Amyloid 1-40 Standard, 1x1vial A2275-73M2: Standard Diluent Buffer, 1x60ml A2275-73M3: Microtiter Plate, 1x96 wells A2275-73M4: beta Amyloid 1-40, Pab 1x6ml A2275-73M5: IgG (HRP) (100X), 1x125ul A2275-73M6: HRP Diluent, 1x25ml A2275-73M7: Wash Buffer (25X), 1x100ml A2275-73M8: TMB, 1x25ml A2275-73M9: Stop Solution, 1x25ml
Storage and Stability
Store *A2275-73M1 powder at 4°C liquid at -70°C. Store other components at 4°C. Stable for at least 6 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
References
1. Savage, M.J., et al. (1998) J. Neurosci. 18:1743-1752. 2. Andreasen, N., et al. (1999) Arch. Neurol. 56(6):673-680. 3. Tan, J., et al. (1999)Science 286(5448):2352-2355. 4. Chishti, M.A., et al. (2001) J. Biol. Chem. 276(24):21562-21570 5. Khan, S.M., et al. (2000) Annals Neurol. 48(2):148-155 6. Kusiak, J.W., et al. (2001) Brain Res. 896:146-152 7. Masliah, E., et al. (2001) Proc. Nat’l. Acad. Sci. 98(21):12245-12250. 8. Monsonego, A., et al. (2001) Proc. Nat’l. Acad. Sci. 98(18):10273-10278 9. Morihara, T., et al. (2002) J. Neurochemistry 83(4):1009-1012 10. Kruman, I.I., et al. (2002) J. Neurosci. 22(5):1752-1762 11. Zheng, H., et al. (2002). J. Neurochem. 80(1):191-196 12. Shie, F.S., et al. (2002) Neuroreport 13(4):455-459 13. Arjona, A.A., et al. (2002) Brain Research 951(1):135-140
USBio References
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