This NCBP2 Cell Based ELISA Kit allows for the detection of NCBP2 and the effects that certain stimulation conditions have on NCBP2 expression in different cell lines. Qualitative determination of NCBP2 concentration is achieved by an indirect ELISA format. In essence, the NCBP2 is captured by Anti-NCBP2 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 NCBP2 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
Recovery
Storage
Store at + 4°C. Stable for 6 months.
Synonyms
20 kDa nuclear cap binding protein, CBC2, CBP20, Cell proliferation inducing gene 55 protein, NCBP 2, NCBP 20 kDa subunit, NCBP interacting protein 1, NIP1, Nuclear cap binding protein subunit 2, PIG55
Disclaimer
This product is for research use only. It is not intended for diagnostic or therapeutic use.
Figure 4: Western Blot - NCBP2 Cell Based ELISA Kit (A103471)
The mouse monoclonal antibody to GAPDH is used as a positive control inNCBP2 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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