Human DAP12 (pY91) ELISA Kit
- SimpleStep
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Human DAP12 (pY91) ELISA Kit is a single-wash 90-min Simplestep used to detect Human DAP12 (pY91). The assay uses a simple mix-wash-read protocol with just one incubation and one wash step.
- Colorimetric Semi-quantitative Sandwich ELISA - 450 nm readout : works on any standard plate reader
View Alternative Names
DAP12, KARAP, TYROBP, TYRO protein tyrosine kinase-binding protein, DNAX-activation protein 12, Killer-activating receptor-associated protein, KAR-associated protein
- sELISA
Supplier Data
Sandwich ELISA - Human DAP12 (pY91) ELISA Kit (AB316133)
Cell line analysis for Human DAP12 Total from preparations of 17,500 cells/well cell extracts. Data from triplicate measurements (mean +/- SD) are plotted.
- sELISA
Supplier Data
Sandwich ELISA - Human DAP12 (pY91) ELISA Kit (AB316133)
Induction of Human DAP12 (pY91) phosphorylation in THP-1 cells in response to pervanadate treatment, and levels of Human DAP12 Total in the same samples. THP-1 cells were added to 96-well tissue culture plates at 2 x 10e6 cells/well and treated (10 min) with a dose-range of pervanadate before cell lysis. Data from duplicate measurements of Human DAP12 (pY91) are plotted and compared against Human DAP12 Total protein levels.
- sELISA
Supplier Data
Sandwich ELISA - Human DAP12 (pY91) ELISA Kit (AB316133)
Example of a typical Human DAP12 (pY91) control lysate dilution series in 1X Cell Extraction Buffer PTR. The DAP12 human lysate dilution series was prepared as described in Section 10. Raw data values are shown in the table.
Reactivity data
Product details
Human DAP12 (pY91) in vitro SimpleStep ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for the semi-quantitative measurement of human DAP12 (pY91) protein in human cells.
The SimpleStep ELISA employs an affinity tag labeled capture antibody and a reporter conjugated detector antibody which immunocapture the sample analyte in solution. This entire complex (capture antibody/analyte/detector antibody) is in turn immobilized via immunoaffinity of an anti-tag antibody coating the well. To perform the assay, samples or controls are added to the wells, followed by the Antibody Cocktail. After incubation, the wells are washed to remove unbound material. TMB substrate is added and during incubation is catalyzed by HRP, generating blue coloration. This reaction is then stopped by addition of Stop Solution completing any color change from blue to yellow. Signal is generated proportionally to the amount of bound analyte and the intensity is measured at 450 nm. Optionally, instead of the endpoint reading, development of TMB can be recorded kinetically at 600 nm.
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Properties and storage information
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Product protocols
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