Lablisa® Human Anti-NMDAR(Anti-N-methyl-D-aspartic Acid Receptor Antibody) ELISA Kit
Product Information
- Description
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The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human Anti-NMDAR. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human Anti-NMDAR. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human Anti-NMDAR, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human Anti-NMDAR in the samples is then determined by comparing the OD of the samples to the standard curve.
Product name: | Human Anti-NMDAR(Anti-N-methyl-D-aspartic Acid Receptor Antibody) ELISA Kit |
Reactivity: | Human |
Alternative Names: | NMDARAb |
Assay Type: | Sandwich |
Sensitivity: | 0.68 ng/mL |
Standard: | 100 ng/mL |
Detection Range: | 1.57-100 ng/mL |
Sample Type: | serum, plasma and other biological fluids |
Assay Length: | 3.5h |
Research Area: | Neuro science; |
Standard curve
Concentration (ng/mL) | OD | Corrected OD |
---|---|---|
100.00 | 2.126 | 2.038 |
50.00 | 1.665 | 1.577 |
25.00 | 1.106 | 1.018 |
12.50 | 0.852 | 0.764 |
6.25 | 0.593 | 0.505 |
3.13 | 0.336 | 0.248 |
1.57 | 0.234 | 0.146 |
0.00 | 0.088 | 0.000 |
Precision
Intra-assay Precision (Precision within an assay):CV%<8%
Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.
Inter-assay Precision (Precision between assays):CV%<10%
Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.
Recovery
Matrices listed below were spiked with certain level of recombinant Anti-NMDAR and the recovery rates were calculated by comparing the measured value to the expected amount of Anti-NMDAR in samples.
Matrix | Recovery range | Average |
---|---|---|
serum(n=5) | 81-93% | 87% |
EDTA plasma(n=5) | 82-94% | 88% |
Heparin plasma(n=5) | 85-97% | 91% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Anti-NMDAR and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Matrix | 1:2 | 1:4 | 1:8 | 1:16 |
---|---|---|---|---|
serum(n=5) | 88-102% | 81-96% | 86-93% | 82-95% |
EDTA plasma(n=5) | 80-94% | 90-99% | 87-103% | 83-96% |
Heparin plasma(n=5) | 91-99% | 88-97% | 88-104% | 97-108% |
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