Manufacturer |
Raybiotech
|
Category |
|
Type |
Elisa |
Specific against |
Human |
Amount |
1 Plate Kit |
Item no. |
PEL-CBL-Y774-T-1 |
eClass 6.1 |
32160605 |
eClass 9.0 |
32160605 |
Available |
|
Compatible Sample Types |
Cell Lysates Tissue Lysates |
Design Principle |
Sandwich-based |
Method of Detection |
Colorimetric |
Quantitative/Semi-Quantitative |
Semi-Quantitative |
Solid Support |
96-well Microplate |
Gene Symbols |
CBLRNF55 |
Kit Components |
Pre- Coated 96-well Strip Microplate Wash Buffer Anti- Phospho Antibody H R P- Conjugated Secondary Antibody Assay Diluent T M B One- Step Substrate Stop Solution Lysis Buffer Positive Control Sample |
Other Materials Required |
Distilled or deionized water100 ml and 1 liter graduated cylinders Tubes to prepare sample dilutions Protease and Phosphatase inhibitors Precision pipettes to deliver 2 µl 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 |
Protocol Outline |
Prepare all reagents and samples as instructed in the manual. Add 100 µl of sample or positive control to each well. Incubate 2.5 h at R T or O/ N at 4 ° C. Add 100 µl of prepared primary antibody to each well. Incubate 1 h at R T. Add 100 µl of prepared 1 X H R P- Streptavidin to each well. Incubate 1 h at R T. Add 100 µl of T M B One- Step Substrate Reagent to each well. Incubate 30 min at R T. Add 50 µl of Stop Solution to each well. Read at 450 nm immediately. |
Product Features |
Rapidly measure phosphorylated protein in lysates Screen numerous different cell lysates without performing a Western Blot analysis Minimal hands-on time, convenient, and non-radioactive material |
Protein Name & Synonyms |
E3 ubiquitin-protein ligase CBL, Casitas B-lineage lymphoma proto-oncogene, Proto-oncogene c-Cbl, RING finger protein 55, RING-type E3 ubiquitin transferase CBL |
Pathway |
B Cell ReceptorHER/ErbB FamilyInsulin SignalingT Cell Receptor |
Introduction |
RayBio® Phospho-CBL (Y774) and Total CBL ELISA kit 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 CBL 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-CBL and total CBL. An anti-pan CBL antibody has been coated onto a 96-well plate. Samples are pipetted into the wells and CBL present in a sample is bound to the wells by the immobilized antibody. The wells are washed and rabbit anti-CBL (Y774) antibody is used to detect phosphorylated CBL or rabbit anti-CBL antibody is used to detect pan CBL. After washing away unbound antibody, HRP-conjugated anti-rabbit IgG is pipetted to 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 CBL (Y774) or pan CBL bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm. |
Positive Control |
K562 cells were treated with Pervanadate (PV). Cells were solubilzed at 4 x 107 cells/ml in Cell Lysate Buffer. Serial dilutions of lysates were analyzed in this ELISA (see Reagent Preparation step 4). |
PV Stimulation of K562 Cell Line |
K562 cells were untreated or treated with PV. Cell lysates were analyzed using this phosphoELISA and Western Blot. |
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.