E11C0007 Bovine Cluster Of Differentiation 8 Bluegene ELISA kit
Bovine Cluster of Differentiation 8 insulin ELISA kit is suitable for the detection of samples from Bovine species. Cluster of Differentiation 8 can also be called P32, CD8-A, Leu2, MAL, T-cell
surface glycoprotein CD8 alpha chain, T-lymphocyte differentiation antigen T8/Leu-2,CD8.
Specifications of Bovine Cluster Of Differentiation 8 ELISA kit
Product Information
Cat. No. E11C0007
Product Name Bovine Cluster of Differentiation 8 ELISA kit
Species Bovine
Product Size 48 Tests / 96 Tests
Concentration 2.5-50 ng/mL
Sensitivity 0.1 ng/mL
Principal Sandwich ELISA
Sample Volume 50 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 10 mL 1 vial
STANDARD A (0.5mL) 0 ng/mL 1 vial
STANDARD B (0.5mL) 2.5 ng/mL 1 vial
STANDARD C (0.5mL) 5 ng/mL 1 vial
STANDARD D (0.5mL) 10 ng/mL 1 vial
STANDARD E (0.5mL) 25 ng/mL 1 vial
STANDARD F (0.5mL) 50 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
CD8 ELISA kit applies the competitive enzyme immunoassay technique utilizing an anti-CD8 antibody and an CD8-HRP conjugate. The assay sample and buffer are incubated together with CD8-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. 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 between CD8 from samples and CD8-HRP conjugate for the anti-CD8 antibody binding site, the intensity of the color is inversely
correlated with the concentration of CD8. As more sites are taken up by CD8 from the sample, fewer sites are left that can bind CD8-HRP conjugate since the number of sites is restricted. A standard
curve is drawn connecting the color's intensity (O.D.) and standard concentration.
Quality Control on Bovine Cluster Of Differentiation 8 ELISA kit
Coefficient of Variance Intra Variation% ＜10%
Inter Variation% ＜12%
Recovery 91-105%
Linearity Diluent Ratio Range %
1:2 88-106
1:4 87-108
1:8 85-110
Specificity/Cross-reactivity No significant cross-reactivity or interference between CD8 and analogues was observed.
