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RayBiotech Human Phospho-eIF-4E (S209) and Total eIF-4E ELISA

Phosphorylation ELISA. Catalog #: PEL-EIF4E-S209-T

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Human Phospho-eIF-4E (S209) and Total eIF-4E ELISA

RayBio® Human Phospho-eIF-4E (S209) and Total eIF-4E ELISA Kit. This assay semi-quantitatively measures phosphorylated eIF-4E (Ser209) and Total eIF-4E in lysate samples.

 

Specifications

Size

1 Plate Kit, 2 Plate Kit, 5 Plate Kit

Species

Human

Quantitative/Semi-Quantitative   

Semi-Quantitative

Protein Name / Synonyms

Eukaryotic translation initiation factor 4E (eIF-4E) (eIF4E) (eIF-4F 25 kDa subunit) (mRNA cap-binding protein)

Specificity

The antibody pair provided in this kit recognizes human eIF-4E phosphorylated at site Serine-209 and total eIF-4E.

Accession Number

P06730

Gene Symbols

EIF4E|EIF4EL1|EIF4F

Gene Id

3287

Compatible Sample Types

Tissue Lysates, Cell Lysates

Solid Support

96-well Microplate

Method Of Detection

Colorimetric

Design Principle

Sandwich-based

Research Area

Post-Translational Modifications, Phosphorylation, Insulin Signaling, Translation

 

Introduction

RayBio® Phospho-eIF4E (Ser209) and Total eIF4E 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 eIF4E 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-eIF4E and total eIF4E. An anti-pan eIF4E antibody has been coated onto a 96-well plate. Samples are pipetted into the wells and eIF4E present in a sample is bound to the wells by the immobilized antibody. The wells are washed and rabbit anti-eIF4E (Ser209) antibody is used to detect phosphorylated eIF4E or rabbit anti-eIF4E antibody is used to detect pan eIF4E. 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 eIF4E (Ser209) or pan eIF4E bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

 

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

 

Application Notes

Kit Components

  • - Pre-Coated 96-well Strip Microplate

  • - Wash Buffer

  • - 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

  • 1. Prepare all reagents and samples as instructed in the manual.

  • 2. Add 100 µl of sample or positive control to each well.

  • 3. Incubate 2.5 h at RT or O/N at 4 °C.

  • 4. Add 100 µl of prepared primary antibody to each well.

  • 5. Incubate 1 h at RT.

  • 6. Add 100 µl of prepared 1X HRP-Streptavidin to each well.

  • 7. Incubate 1 h at RT.

  • 8. Add 100 µl of TMB One-Step Substrate Reagent to each well.

  • 9. Incubate 30 min at RT.

  • 10. Add 50 µl of Stop Solution to each well.

  • 11. Read at 450 nm immediately.

 

Typical Data

Positive Control

HeLa cells were treated with Anisomycin. 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.

Anisomycin Stimulation of HeLa Cell Lines

HeLa cells were treated or untreated with Anisomycin. 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.

Catalog #: PEL-EIF4E-S209-T-1 -- 1 Plate Kit

Catalog #: PEL-EIF4E-S209-T-2 -- 2 Plate Kit

Catalog #: PEL-EIF4E-S209-T-5 -- 5 Plate Kit

 

Please email us at cs@medikonia.com for any enquiry. To place an order, please include the catalog number(s) of the product(s) in the email.