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ELK Biotechnology
SKU:ELK8248
Human Anti-GRIN2A(Anti-Glutamate Receptor, Ionotropic, N-Methyl-D-Aspartate 2A Antibody) ELISA Kit
Human Anti-GRIN2A(Anti-Glutamate Receptor, Ionotropic, N-Methyl-D-Aspartate 2A Antibody) ELISA Kit
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$458.00 USD
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Human Anti-GRIN2A(Anti-Glutamate Receptor, Ionotropic, N-Methyl-D-Aspartate 2A Antibody) ELISA Kit
Overview
| Product name: | Human Anti-GRIN2A(Anti-Glutamate Receptor, Ionotropic, N-Methyl-D-Aspartate 2A Antibody) ELISA Kit |
| Reactivity: | Human |
| Alternative Names: | NMDAR2A; NR2A; Glutamate [NMDA] receptor subunit epsilon-1; N-methyl D-aspartate receptor subtype 2A |
| Assay Type: | Competitive Inhibition |
| Sensitivity: | 1.33 ng/mL |
| Standard: | 200 ng/mL |
| Range: | 3.13-200 ng/mL |
| Sample Type: | serum, plasma and other biological fluids |
| Assay Length: | 2h, 30min |
| Research Area: | Neuro science; |
| Test principle: | This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human Anti-GRIN2A protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human Anti-GRIN2A. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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-GRIN2A in the samples is then determined by comparing the OD of the samples to the standard curve. |
Standard curve
| Concentration (ng/mL) | OD | Corrected OD |
|---|---|---|
| 200.00 | 0.155 | — |
| 100.00 | 0.386 | — |
| 50.00 | 0.524 | — |
| 25.00 | 0.812 | — |
| 12.50 | 1.139 | — |
| 6.25 | 1.557 | — |
| 3.13 | 1.697 | — |
| 0.00 | 2.112 | — |

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-GRIN2A and the recovery rates were calculated by comparing the measured value to the expected amount of Anti-GRIN2A in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 82-95% | 88% |
| EDTA plasma(n=5) | 88-102% | 95% |
| Heparin plasma(n=5) | 95-107% | 101% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Anti-GRIN2A 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) | 98-106% | 86-102% | 88-96% | 89-97% |
| EDTA plasma(n=5) | 85-94% | 87-103% | 82-94% | 78-90% |
| Heparin plasma(n=5) | 85-94% | 97-103% | 79-91% | 82-91% |
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