Description
Human and Mouse Phosphotyrosine CSK PharmaGenie ELISA Kit (SBRS1780)
Product SKU: | SBRS1780 |
Size: | 96T |
Application: | This ELISA kit recognizes human CSK phosphotyrosine. |
Uniprot: | P41240 / P41241 |
Gene ID: | 1445 |
Gene Names: | CSK |
Pathway: | Tyrosine Kinase Family |
Synonyms: | Tyrosine-protein kinase CSK (EC 2.7.10.2) (C-Src kinase) (Protein-tyrosine kinase CYL) |
Target Species: | Human, Mouse |
Compatible Sample Types: | Cell Lysates, Tissue Lysates |
Design Principle: | Sandwich-based |
Method of Detection: | Colorimetric |
Quantitative/Semi-Quantitative: | Semi-Quantitative |
Storage/Stability: | Upon receipt, the kit should be stored at -20°C. Please use within 6 months from the date of shipment. |
- Pre-Coated 96-well Strip Microplate
- Wash Buffer
- Biotinylated Anti-Phosphotyrosine Antibody
- Stop Solution
- Assay Diluent(s)
- Positive Control Sample
- Lysis Buffer
- Streptavidin-Conjugated HRP
- TMB One-Step Substrate
Other materials and equipment required:
The Assay Genie Human and Mouse Phosphotyrosine CSK PharmaGenie ELISA Kit (SBRS1780) will require other equipment and materials to carry out the assay. Please see list below for further details.
- Distilled or deionized water
- 100 ml and 1 liter graduated cylinders
- Tubes to prepare sample dilutions
- Protease and Phosphatase inhibitors
- Precision pipettes to deliver 2 ul to 1 ml volumes
- Adjustable 1-25 ml pipettes for reagent preparation
- Benchtop rocker or shaker
- Microplate reader capable of measuring absorbance at 450 nm
- Prepare all reagents and samples as instructed in the manual.
- Add 100 ul of sample or positive control to each well.
- Incubate 2.5 h at RT or O/N at 4 °C.
- Add 100 ul of prepared primary antibody to each well.
- Incubate 1 h at RT.
- Add 100 ul of prepared 1X HRP-Streptavidin to each well.
- Incubate 1 h at RT.
- Add 100 ul of TMB One-Step Substrate Reagent to each well.
- Incubate 30 min at RT.
- Add 50 ul of Stop Solution to each well.
- Read at 450 nm immediately.
Jurkat cells were treated with Pervanadate. Cell lysates were analyzed using this phosphoELISA and Western Blot. | |
Jurkat cells were treated with Pervanadate. Solubilize cells at 4 x 107 cells/ml in Cell Lysate Buffer. Serial dilutions of lysates were analyzed in this ELISA. |