E03P1047 Mouse Phosphorylated AKT1 Kinase ELISA kit
The Mouse Phosphorylated AKT1 Kinase ELISA kit can be used to identify samples from the mouse species. Phosphorylated AKT1 Kinase can also be called p-AKT.
E03P1047 Mouse Phosphorylated AKT1 Kinase ELISA kit
The Mouse Phosphorylated AKT1 Kinase ELISA kit can be used to identify samples from the mouse species. Phosphorylated AKT1 Kinase can also be called p-AKT.
Product Information | |
Cat. No. | E03P1047 |
Product Name | Mouse Phosphorylated AKT1 Kinase ELISA kit |
Species | Mouse |
Product Size | 48 Tests / 96 Tests |
Concentration | 0.5-10ng/ml |
Sensitivity | 0.1ng/ml |
Principal | Competitive ELISA |
Sample Volume | 100 ul |
Sample Type | Serum, plasma, cell culture supernatants, body fluid and tissue homogenate |
Assay Time | 90 minutes |
Platform | Microplate Reader |
Conjugate | HRP |
Detection Method | Colorimetric |
Storage | 2-8°C |
Kit Components | ||
MATERIALS | SPECIFICATION | QUANTITY |
MICROTITER PLATE | 96 wells | stripwell |
ENZYME CONJUGATE | 6.0 mL | 1 vial |
STANDARD A (0.5mL) | 0 ng/ml | 1 vial |
STANDARD B (0.5mL) | 0.5 ng/ml | 1 vial |
STANDARD C (0.5mL) | 1.0 ng/ml | 1 vial |
STANDARD D (0.5mL) | 2.5 ng/ml | 1 vial |
STANDARD E (0.5mL) | 5.0 ng/ml | 1 vial |
STANDARD F (0.5mL) | 10 ng/ml | 1 vial |
SUBSTRATE A | 6 mL | 1 vial |
SUBSTRATE B | 6 mL | 1 vial |
STOP SOLUTION | 6 mL | 1 vial |
WASH SOLUTION (100 x) | 10 mL | 1 vial |
BALANCE SOLUTION | 3 mL | 1 vial |
Principle of the Assay |
p-AKT ELISA kit applies the competitive enzyme immunoassay technique utilizing an anti-p-AKT antibody and a p-AKT-HRP conjugate. The assay sample and buffer are incubated together with p-AKT-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the p-AKT concentration since p-AKT from samples and p-AKT-HRP conjugate compete for the anti-p-AKT antibody binding site. Since the number of sites is limited, as more sites are occupied by p-AKT from the sample, fewer sites are left to bind p-AKT-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The p-AKT concentration in each sample is interpolated from this standard curve. |
Coefficient of Variance | Intra Variation% <10% | |
Inter Variation% <12% | ||
Recovery | 95-102% | |
Linearity | Diluent Ratio | Range % |
1:2 | 93-105 | |
1:4 | 88-106 | |
1:8 | 86-108 | |
Specificity/Cross-reactivity | No significant cross-reactivity or interference between p-AKT and analogues was observed. |
E03P1047 has been referenced in the below publications:
Study on inhibitory mechanism of polypeptide extract from scorpion venom on ovarian cancer.
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