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Neuroscience Neurotransmission Intracellular Signaling Kinases

Phospho-ERK2 (T185/Y187) and Total ERK2 ELISA Kit (ab279794)

Phospho-ERK2 (T185/Y187) and Total ERK2 ELISA Kit (ab279794)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Sample type: Cell Lysate
  • Detection method: Colorimetric
  • Assay type: Semi-quantitative
  • Reacts with: Human

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Overview

  • Product name

    Phospho-ERK2 (T185/Y187) and Total ERK2 ELISA Kit
    See all ERK2 kits
  • Detection method

    Colorimetric
  • Sample type

    Cell Lysate
  • Assay type

    Semi-quantitative
  • Assay duration

    Multiple steps standard assay
  • Species reactivity

    Reacts with: Human
  • Product overview

    Phospho-ERK2 (T185/Y187) and Total ERK2 (ab279794) is a very rapid, convenient, and sensitive assay kit that can monitor the activation or function of important biological pathways in mouse cell lysates. By determining phosphorylated ERK2 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 mouse phospho-ERK2 and total ERK2. An anti-pan ERK2 antibody has been coated onto a 96-well plate. Samples are pipetted into the wells and ERK2 present in a sample is bound to the wells by the immobilized antibody and the wells are washed. In select wells, rabbit anti-phospho ERK2 (T185/Y187) antibody is added to detect phosphorylated ERK2. In the remaining wells, biotinylated anti-pan-ERK2 antibody is used to detect pan ERK2. After washing away unbound antibody, HRP-conjugated anti-rabbit IgG or Streptavidin-Conjugated HRP 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 ERK2 (T185/Y187) or pan ERK2 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

  • Tested applications

    Suitable for: Sandwich ELISAmore details
  • Platform

    Pre-coated microplate (12 x 8 well strips)

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 1 x 96 tests
    20X Wash Buffer Concentrate 1 x 25ml
    2X Cell lysate buffer 1 x 10ml
    300X Streptavidin-Conjugated HRP 1 vial
    5X Assay Diluent 1 x 15ml
    Biotinylated anti-pan-ERK2 detection antibody 1 vial
    HRP-conjugated anti-rabbit IgG concentrate (1000X) 1 vial
    Pan-ERK2 Coated Microplate 1 unit
    Positive Control - NIH/3T3 cell lysate 1 vial
    Rabbit anti-phospho-ERK2 (T185/Y187)-antibody 1 vial
    Stop Solution 1 x 8ml
    TMB One-Step Substrate Reagent 1 x 12ml
  • Research areas

    • Neuroscience
    • Neurotransmission
    • Intracellular Signaling
    • Kinases
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • MAPK Pathway
    • Stem Cells
    • Signaling Pathways
    • TGF beta
    • Cytoplasmic
  • Function

    Involved in both the initiation and regulation of meiosis, mitosis, and postmitotic functions in differentiated cells by phosphorylating a number of transcription factors such as ELK1. Phosphorylates EIF4EBP1; required for initiation of translation. Phosphorylates microtubule-associated protein 2 (MAP2). Phosphorylates SPZ1 (By similarity). Phosphorylates heat shock factor protein 4 (HSF4) and ARHGEF2.
    Acts as a transcriptional repressor. Binds to a [GC]AAA[GC] consensus sequence. Repress the expression of interferon gamma-induced genes. Seems to bind to the promoter of CCL5, DMP1, IFIH1, IFITM1, IRF7, IRF9, LAMP3, OAS1, OAS2, OAS3 and STAT1. Transcriptional activity is independent of kinase activity.
  • Sequence similarities

    Belongs to the protein kinase superfamily. CMGC Ser/Thr protein kinase family. MAP kinase subfamily.
    Contains 1 protein kinase domain.
  • Domain

    The TXY motif contains the threonine and tyrosine residues whose phosphorylation activates the MAP kinases.
  • Post-translational
    modifications

    Dually phosphorylated on Thr-185 and Tyr-187, which activates the enzyme. Dephosphorylated by PTPRJ at Tyr-187.
  • Cellular localization

    Nucleus.
  • Target information above from: UniProt accession P28482 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Alternative names

    • ERK 2
    • ERK-2
    • ERT1
    • Extracellular Signal Regulated Kinase 2
    • Extracellular signal-regulated kinase 2
    • MAP kinase 1
    • MAP kinase 2
    • MAP kinase isoform p42
    • MAPK 1
    • MAPK 2
    • Mapk1
    • MAPK2
    • Mitogen-activated protein kinase 1
    • Mitogen-activated protein kinase 2
    • MK01_HUMAN
    • P38
    • P40
    • P41
    • p42-MAPK
    • P42MAPK
    • PRKM1
    • PRKM2
    • protein kinase, mitogen-activated, 1
    • protein kinase, mitogen-activated, 2
    • protein tyrosine kinase ERK2
    see all
  • Database links

    • Entrez Gene: 5594 Human
    • Omim: 176948 Human
    • SwissProt: P28482 Human
    • Unigene: 431850 Human

    Images

    • Positive Control
      Positive Control

      NIH/3T3 cells were treated with PDGFBB at 37°C for 20 min.

      Cells were solubilzed at 4 x 107 cells/ml in Cell Lysate Buffer.

    • NIH/3T3 cells treated with/without PDGF.
      NIH/3T3 cells treated with/without PDGF.
      NIH/3T3 cells were untreated or treated with 50 ng/ml PDGFBB for 10 mins.
    • NIH/3T3 cells treated with/without PDGF.
      NIH/3T3 cells treated with/without PDGF.
      NIH/3T3 cells were untreated or treated with 50 ng/ml PDGFBB for 10 mins.

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
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