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Principle
This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with GC protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to GC. 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 stop solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of GC in the samples is then determined by comparing the OD of the samples to the standard curve.
Specification
Product name | Quanticon Human GC(Glucagon) ELISA Kit |
SKU | ABQ-EC96-GChu |
Applications | ELISA |
Reactivity | Human |
Alternative Name | Carbohydrate-Rich Portion of Platelet Membrane Glycoprotein Ib Alpha Polypeptide |
Standard | 2000pg/mL |
Sensitivity | 18.75 pg/mL |
Detection Range | 31.25-2000pg/mL |
Sample Type | Serum, Plasma, Tissue homogenate and Other biological samples |
Sample Volume | 50 μL |
Assay Type | Competitive |
Assay Duration | 1.5H |
Detection Wavelength | 450nm |
Storage | 2-8oC/-20 oC |
PRECISION
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level were tested on 3 different plates, 20 replicates in each plate, respectively.
Item | Intra-assay Precision | Intra-assay Precision |
Sample | 3 | 3 |
Replicate | 9 | 18 |
CV(%) | 5 | 8 |
Rate of recovery
The recovery of spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
Sample Type | Range(%) | Average Recovery(%) |
Serum (n=8) | 80-95 | 87 |
EDTA plasma (n=8) | 80-96 | 87 |
Cell culture media (n=8) | 80-92 | 85 |
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