E02A0690 Rat Arachidonic Acid ELISA kit
The Rat Arachidonic Acid ELISA kit can be used to identify samples from the rat species. Arachidonic Acid can also be called arachidonic acid, arachidonate, (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoic acid, AA.
E02A0690 Rat Arachidonic Acid ELISA kit
The Rat Arachidonic Acid ELISA kit can be used to identify samples from the rat species. Arachidonic Acid can also be called arachidonic acid, arachidonate, (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoic acid, AA.
Product Information | |
Cat. No. | E02A0690 |
Product Name | Rat Arachidonic Acid ELISA kit |
Species | Rat |
Product Size | 48 Tests / 96 Tests |
Concentration | 1.0-25 ng/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) | 1.0 ng/mL | 1 vial |
STANDARD C (0.5mL) | 2.5 ng/mL | 1 vial |
STANDARD D (0.5mL) | 5.0 ng/mL | 1 vial |
STANDARD E (0.5mL) | 10 ng/mL | 1 vial |
STANDARD F (0.5mL) | 25 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 |
AA ELISA kit uses an anti-AA antibody and an AA-HRP conjugate in a competitive enzyme immunoassay method. AA-HRP conjugate is incubated with the assay sample and buffer in a pre-coated plate for one hour. The wells are decanted and washed five times when the incubation period is over. The HRP enzyme substrate is then incubated in the wells. The result of the enzyme-substrate reaction is a complex that is blue in hue. The process is finally stopped by adding a stop solution, causing the solution to turn yellow. In a microplate reader, the color intensity is measured spectrophotometrically at 450 nm. Due to competition for the anti-AA antibody binding site between AA from samples and AA-HRP conjugate, the intensity of the color is inversely proportional to the concentration of AA. Since the number of sites is limited, as more sites are occupied by AA from the sample, fewer sites are left to bind AA-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The AA 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 AA and analogues was observed. |
E02A0690 has been referenced in the below publications:
RhoA/Rho Kinase Mediates Neuronal Death Through Regulating cPLA2 Activation.
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