Human/Mouse/Rat Phospho-JNK (T183/Y185) and Total JNK ELISA

RayBio® Human/Mouse/Rat Phospho-JNK (T183/Y185) and Total JNK ELISA Kit. This assay semi-quantitatively measures phosphorylated JNK (Thr183/Tyr185) and Total JNK in lysate samples.

PEL-JNK-T183-T-1
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Antigen Information

Accession Number:
  • P45983
Gene ID:
  • 5599
Gene Symbols:
  • JNK1
  • MAPK8
  • PRKM8
  • SAPK1
  • SAPK1C
Protein Name & Synonyms:
Mitogen-activated protein kinase 8 (MAP kinase 8) (MAPK 8) (EC 2.7.11.24) (JNK-46) (Stress-activated protein kinase 1c) (SAPK1c) (Stress-activated protein kinase JNK1) (c-Jun N-terminal kinase 1)

Assay Format

Pathway:
  • MAPK Signaling
Specificity:
The antibody pair provided in this kit recognizes Human/Mouse/Rat Phospho-JNK (pThr183/Tyr185) and total (pan) JNK.
Number of Targets Detected:
2
Species Detected:
  • Human
  • Mouse
  • Rat
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

Product Specifications

Size:
1, 2, or 5 x 96-Well Strip Microplate Kit

Introduction

RayBio® Phospho- JNK (T183/Y185) ELISA kit is a very rapid, convenient and sensitive assay kit that can monitor the activation or function of important biological pathways in human, mouse and rat cell lysates. By determining phosphorylated JNK 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, mouse and rat phospho-JNK. An anti-pan JNK antibody has been coated onto a 96-well plate. Samples are pipetted into the wells and JNK present in a sample is bound to the wells by the immobilized antibody. The wells are washed and rabbit anti-JNK (T183/Y185) antibody is used to detect phosphorylated JNK. 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 JNK (T183/Y185) bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

Product Features

  • Simultaneously measure Phosphorylated protein and pan protein in one experiment (for normalization purpose)
  • Screen numerous different cell lysates without performing a Western Blot analysis
  • Minimal hands-on time, convenient, and non-radioactive material

Application Notes

Kit Components
  • Pre-Coated 96-well Strip Microplate
  • Wash Buffer
  • li id="">Anti-Phospho Antibody
  • Anti-Pan Antibody
  • HRP-Conjugated Secondary Antibody
  • Streptavidin-Conjugated HRP
  • Assay Diluent
  • TMB One-Step Substrate
  • Stop Solution
  • Lysis Buffer
  • Positive Control Sample
Other Materials Required
  • 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 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
    li id="aeaoofnhgocdbnbeljkmbjdmhbcokfdb-mousedown">Prepare all reagents and samples as instructed in the manual.
  1. Add 100 ?l of sample or positive control to each well.
  2. Incubate 2.5 h at RT or O/N at 4 ?C.
  3. Add 100 ?l of prepared primary antibody to each well.
  4. Incubate 1 h at RT.
  5. Add 100 ?l of prepared 1X HRP-Streptavidin to each well.
  6. Incubate 1 h at RT.
  7. Add 100 ?l of TMB One-Step Substrate Reagent to each well.
  8. Incubate 30 min at RT.
  9. Add 50 ?l of Stop Solution to each well.
  10. Read at 450 nm immediately.

Typical Data

Positive Control
HepG2 cells were treated with IL-1Β at 37oC for 30 min. Solubilize cells at 4 x 107 cells/ml in Cell Lysate Buffer. Serial dilutions of lysates were analyzed in this ELISA. Please see step 3 of Part VI Reagent Preparation for detail.
IL-1Β Stimulation of HepG2 Cell Line
HepG2 cells were treated or untreated with 25ng/ml IL-1Β for 30 min. Cell lysates were analyzed using this phosphoELISA and Western Blot.


Storage/Stability

Upon receipt, the kit should be stored at –20°C. Please use within 6 months from the date of shipment. After initial use, Wash Buffer Concentrate (Item B), Assay Diluent (Item E), TMB One-Step Substrate Reagent (Item H), Stop Solution (Item I) and Cell Lysate Buffer (Item J) should be stored at 4°C to avoid repeated freeze-thaw cycles. Return unused wells to the pouch containing desiccant pack, reseal along entire edge, and store at –20°C. Item D, store at 2-8°C for up to one month (store at -20°C for up to 6 months, avoid repeated freeze-thaw cycles). Reconstituted Positive Control (Item K) should be stored at -70°C.

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Usage

This product is furnished for LABORATORY RESEARCH USE ONLY.
Not for diagnostic or therapeutic use.