Instant ELISA Kit for Interleukin 8 (IL8)

Homo sapiens (Human)

1h, 10min

This assay has high sensitivity and excellent specificity for detection of Instant Interleukin 8 (IL8).
No significant cross-reactivity or interference between Instant Interleukin 8 (IL8) and analogues was observed.

The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

The test principle applied in this kit is enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Instant Interleukin 8 (IL8). Standards or samples and HRP-labeled detection antibody specific to Instant Interleukin 8 (IL8) (Detection Reagent A) are then added to the appropriate microtiter plate wells. Next, TMB substrate solution is added, only those wells that contain Instant Interleukin 8 (IL8), and HRP-labeled detection antibody will exhibit a change in color. 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 Instant Interleukin 8 (IL8) in the samples is then determined by comparing the O.D. of the samples to the standard curve.