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ab126420 is a very rapid, convenient and sensitive assay kit that can monitor the activation or function of important biological pathways in cells. It can be used for measuring the relative amount of EGFR (Tyr1068) phosphorylation and screening the effects of various treatments, inhibitors (such as siRNA or chemicals), or activators in cultured Human cell lines. By determining EGFR protein phosphorylation in your experimental model system, you can verify pathway activation in your cell lines without spending excess time and effort in preparing cell lysate and performing an analysis of Western Blot.
In the EGFR (Tyr1068) Human In-Cell ELISA Kit, cells are seeded into a 96 well tissue culture plate. The cells are fixed after various treatments, inhibitors or activators. After blocking, anti-Phospho-EGFR (Tyr1068) or anti-EGFR (primary antibody) is pipetted into the wells and incubated. The wells are washed, and HRP-conjugated anti-rabbit IgG (secondary antibody) is added to the wells. The wells are washed again, a TMB substrate solution is added to the wells and color develops in proportion to the amount of protein. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.
|Components||1 x 96 tests|
|Anti-Rabbit IgG Concentrate (Item I-1)||1 x 10µl|
|5X Blocking Buffer Concentrate (Item F)||1 x 20ml|
|Fixing Solution (Item D)||1 x 30ml|
|Uncoated 96-well Microplate (Item A)||1 unit|
|Quenching Buffer Concentrate (30x) (Item E)||1 x 2ml|
|Rabbit Anti-EGFR Concentrate (Item H)||1 x 6µl|
|Rabbit Anti-Phospho-EGFR (Tyr1068) Concentrate (Item G)||1 x 6µl|
|Stop Solution||1 x 14ml|
|TMB One-Step Substrate Reagent||1 x 12ml|
|20X Wash Buffer A Concentrate (Item B)||1 x 30ml|
|20X Wash Buffer B Concentrate (Item C)||1 x 30ml|
Our Abpromise guarantee covers the use of ab126420 in the following tested applications.
|In-Cell ELISA||Use at an assay dependent concentration.|
A431 cells were stimulated by different concentrations of EGF for 10 min at 37°C.
ab126420 has not yet been referenced specifically in any publications.