This ATRIP Cell Based ELISA Kit allows for the detection of ATRIP and the effects that certain stimulation conditions have on ATRIP expression in different cell lines. Qualitative determination of ATRIP concentration is achieved by an indirect ELISA format. In essence, the ATRIP is captured by Anti-ATRIP Antibodies which in turn are detected by HRP-conjugated secondary antibodies. Through this binding, the HRP enzyme (conjugated to the secondary antibody) can catalyze a colorimetric reaction upon substrate addition. Due to the qualitative nature of this ATRIP Cell Based ELISA Kit, multiple normalization methods are described: 1) Anti-GAPDH Antibody is included to serve as an internal positive control in normalizing the target absorbance values. 2) Following the colorimetric measurement of HRP activity via substrate addition, the Crystal Violet whole-cell staining method is used to determine cell density. After staining, the results can be analyzed by normalizing the absorbance values to cell amounts, by which the plating difference can be adjusted.
Platform
Microplate
Detection Type
Colorimetric
Sample Type
Adherent cells and suspension cells.
Product Range
> 5000 Cells
Assay Time
4 hours 30 minutes
Reactivity
Human, Mouse, Rat
Recovery
Storage
Store at + 4°C. Stable for 6 months.
Synonyms
AGS1, ATIP, ATM and Rad3 related interacting protein, ATM and Rad3-related-interacting protein, ATR interacting protein, ATR-interacting protein, ATRIP_HUMAN, DKFZp762J2115, FLJ12343, MGC20625, MGC21482, MGC26740
Disclaimer
This product is for research use only. It is not intended for diagnostic or therapeutic use.
Figure 4: Western Blot - ATRIP Cell Based ELISA Kit (A103055)
The mouse monoclonal antibody to GAPDH is used as a positive control inATRIP Cell Based ELISA Kit. Anti-GAPDH Antibody was tested for specificity by western blot with tissue lysates from human, mouse, and rat.
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