ELISA/assay

Mouse amyloid beta peptide 1-40 ELISA Kit

MBS732452

48-Strip-Wells

470 USD

ELISA Kit

Mouse amyloid beta peptide 1-40 ELISA Kit

amyloid beta peptide 1-40

Mouse amyloid beta peptide 1-40 ELISA Kit; amyloid beta peptide 1-40; amyloid beta peptide 1-40 (Mouse)

Abeta1-40

Ab1-40; A 1-40

Mouse

This assay has high sensitivity and excellent specificity for detection of Abeta1~40. No significant cross-reactivity or interference between Abeta1~40 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between Abeta1~40 and all the analogues, therefore, cross reaction may still exist in some cases.

Store all reagents at 2-8 degree C

Samples: Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate. Assay Type: Sandwich. Sensitivity: 1.0 pg/mL.

Intended Uses: This Abeta1~40 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse Abeta1~40. This ELISA kit for research use only, not for therapeutic or diagnostic applications!

Mouse ELISA Kit

Principle of the assay: Abeta1~40 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for Abeta1~40. Standards or samples are then added to the microtiter plate wells and Abeta1~40 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of Abeta1~40 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for Abeta1~40 are added to each well to "sandwich" the Abeta1~40 immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain Abeta1~40 and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The Abeta1~40 concentration in each sample is interpolated from this standard curve.

48-Strip-Wells

470 USD

96-Strip-Wells

675