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Intra-assay Precision (Precision within an assay): CV%<15% | ||||||
Three samples of known concentration were tested twenty times on one plate to assess. | ||||||
Inter-assay Precision (Precision between assays): CV%<15% | ||||||
Three samples of known concentration were tested in twenty assays to assess. | ||||||
To assess the linearity of the assay, samples were spiked with high concentrations of mouse C-Peptide in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay. | ||||||
Sample | Serum(n=4) | |||||
1:1 | Average % | 93 | ||||
Range % | 85-99 | |||||
1:2 | Average % | 90 | ||||
Range % | 85-96 | |||||
1:4 | Average % | 95 | ||||
Range % | 87-106 | |||||
1:8 | Average % | 95 | ||||
Range % | 89-100 |
The recovery of mouse C-Peptide spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section. | ||||||
Sample Type | Average % Recovery | Range | ||||
Serum (n=5) | 96 | 89-100 | ||||
EDTA plasma (n=4) | 95 | 91-103 | ||||
A micro ELISA plate ---The 96-well plate has been pre-coated with an anti-mouse C-peptide antibody.
Six vials lyophilized standard ---Dilute a bottle of the standard at dilution series, read the OD values, and then draw a standard curve.
One vial HRP-conjugated C-peptide antibody(6 ml/bottle) ---Bind to the C-peptide in the samples or standards and react with the substrate to make the solution chromogenic.
One vial Wash Buffer (20x concentrate) (15ml/bottle) ---Wash away unbound or free substances.
Substrate A (1 x 7 ml)
Substrate B (1 x 7 ml)
A microplate reader capable of measuring absorbance at 450 nm, with the correction wavelength set at 600 nm or 630 nm.
An incubator can provide stable incubation conditions up to 37°C±5°C.
Centrifuge
Vortex
Squirt bottle, manifold dispenser, or automated microplate washer
Absorbent paper for blotting the microtiter plate
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