Phospho-CD167a/DDR1 (Y792) and Total CD167a/DDR1 ELISA Kit
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- sELISA
Supplier Data
Sandwich ELISA - Phospho-CD167a/DDR1 (Y792) and Total CD167a/DDR1 ELISA Kit (AB279769)
Jurkat cells were treated with/without Calyculin A and Pervanadate. Jurkat cells were treated with Calyculin A and Pervanadate.
- sELISA
Supplier Data
Sandwich ELISA - Phospho-CD167a/DDR1 (Y792) and Total CD167a/DDR1 ELISA Kit (AB279769)
Positive Control.
Jurkat cells were treated with Calyculin A and Pervanadate.
Solubilize cells at 4 x 107 cells/ml in Cell Lysate Buffer.
Serial dilutions of lysates were analyzed in this ELISA.
- sELISA
Supplier Data
Sandwich ELISA - Phospho-CD167a/DDR1 (Y792) and Total CD167a/DDR1 ELISA Kit (AB279769)
Jurkat cells were treated with/without Calyculin A and Pervanadate. Jurkat cells were treated with Calyculin A and Pervanadate.
Reactivity data
Product details
PhosphoCD167a/DDR1 (Y792) and Total CD167a/DDR1 ELISA Kit (ab279769) is a very rapid, convenient, and sensitive assay kit that can monitor the activation or function of important biological pathways in human cell lysates. By determining phosphorylated CD167a/DDR1 protein in your experimental model system, you can verify pathway activation in your cell lysates. You can simultaneously measure numerous different cell lysates without spending excess time and effort in performing a Western Blotting analysis.
This Sandwich ELISA kit is an in vitro enzyme-linked immunosorbent assay for the measurement of human phospho-CD167a/DDR1 (Y792) and total CD167a/DDR1. An anti-pan CD167a/DDR1 antibody has been coated onto a 96-well plate. Samples are pipetted into the wells and CD167a/DDR1 present in a sample is bound to the wells by the immobilized antibody and the wells are washed. In select wells, rabbit anti-phospho CD167a/DDR1 (Y792) antibody is added to detect phosphorylated CD167a/DDR1. In the remaining wells, rabbit anti-pan-CD167a/DDR1 antibody is used to detect pan CD167a/DDR1 . After washing away unbound antibody, HRP-conjugated anti-rabbit IgG is pipetted into the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of CD167a/DDR1 (Y792) or pan CD167a/DDR1 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
CD167a/DDR1 modulates interactions between cells and their surrounding matrix. It is involved in a complex with collagen mediating signal transduction processes. This interaction is important for cellular biophysical responses driving processes like cell migration and differentiation. In marmoset thyroid tissue DDR1 helps maintain structural integrity and regulates cellular activities important for normal thyroid function.
Pathways
CD167a/DDR1 participates in key signaling pathways including those related to cell adhesion and extracellular matrix remodeling. Specifically it operates within the MAPK/ERK pathway influencing cell cycle dynamics and responses to stress signals. DDR1 also interacts with proteins like SHC and Ras enabling communication between the cell surface and intracellular targets necessary for growth and adaptation.
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