This ITPK1 Cell Based ELISA Kit allows for the detection of ITPK1 and the effects that certain stimulation conditions have on ITPK1 expression in different cell lines. Qualitative determination of ITPK1 concentration is achieved by an indirect ELISA format. In essence, the ITPK1 is captured by Anti-ITPK1 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 ITPK1 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.
Western Blot - ITPK1 Cell Based ELISA Kit (A103477)
Western blot analysis of extracts from HeLa/HepG2/Jurkat cells, using Anti-ITPK1 Antibody. The lane on the right is treated with the synthesized peptide.
Western Blot - ITPK1 Cell Based ELISA Kit (A103477)
The mouse monoclonal antibody to GAPDH is used as a positive control inITPK1 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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Proteins predicted to interact with ITPK1
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.