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Anti-MAP Kinase, Non-Phosphorylated ERK antibody, Mouse monoclonal

SIGMA/M3807 - clone ERK-NP2, purified from hybridoma cell culture

Synonym: Anti-ERK; Anti-ERK-2; Anti-ERK2; Anti-ERT1; Anti-MAPK2; Anti-NS13; Anti-P42MAPK; Anti-PRKM1; Anti-PRKM2; Anti-p38; Anti-p40; Anti-p41; Anti-p41mapk; Anti-p42-MAPK

MDL Number: MFCD02096849
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-M3807-.2ML 0.2 mL
$830.00
1/EA
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Immunoblotting Whole extract of Rat brain was separated on SDS-PAGE, blotted with 5 μg/mL Monoclonal Anti-MAP Kinase Clone: ERK-NP2 (Cat. No. M3807) and developed using Goat Anti-Mouse IgG-ALP (Cat. No. A2179) and a NBT/BCIP (Cat. No. B5655) substrate.
Immunoprecipitation Monoclonal Anti-MAP Kinase, Non-Phosphorylated ERK, Clone: ERK-NP2 (Cat. No. M3807) was used to immunoprecipitate MAPK1/MAPK3 from HeLa whole cell lysate. Detection antibody: Rabbit Anti-MAP Kinase (ERK-1, ERK-2) (Cat. No. M5670) followed by Goat Anti-Rabbit IgG-peroxidase (Cat. No. A0545) and a chemiluminescent substrate. Lanes 1. 10 μg antibody 2. Negative control: 10 μg nonrelevant antibody 3. Positive control: HeLa whole cell lysate

 

antibody form purified from hybridoma cell culture
antibody product type primary antibodies
biological source mouse
clone ERK-NP2, monoclonal
concentration ~2 mg/mL
conjugate unconjugated
form buffered aqueous solution
isotype IgG1
mol wt antigen, ERK-1 44 kDa
  antigen, ERK-2 42 kDa
Quality Level 200 
shipped in dry ice
species reactivity human, rat
storage temp. −20°C
target post-translational modification unmodified
technique(s) immunocytochemistry: suitable
  indirect ELISA: suitable
  microarray: suitable
  western blot: 5-25 μg/mL using rat brain extract
UniProt accession no. P28482 
Application: A working concentration of 5-25 μg/mL may be used for detection by immunoblotting in rat brain extract. The antibody has also been used at working dilution of 1:50 for MAPK quantification by flow cytometry in monocyte-derived macrophages (MDM) derived from Holstein cattle.
Biochem/physiol Actions: The antibody reacts specifically with the non-phosphorylated, non-activated form of MAP kinase (ERK-1 and ERK-2). Weak cross-reaction is observed with monophosphorylated (threonine or tyrosine), but not with diphosphorylated peptides of MAPK. The antibody does not recognize JNK or p38 MAPK. The epitope recognized by the antibody contains non-phosphorylated threonine 183 and tyrosine 185 which resides within the ERK-activation loop (e.g., amino acids 178-188 in ERK-2).
Disclaimer: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
General description: Mitogen-activated protein kinase (MAPK) superfamily of enzymes is involved in widespread signalling pathways. Members of this family include the ERK1/2 (extracellular signal-regulated protein kinase, also termed p42/p44 MAPK), JNK and p38 MAPK subfamilies. These are the terminal enzymes in a signalling cascade where each kinase phosphorylates and activates the next member in the sequence. Phosphorylation of both tyrosine and threonine is essential for the full activation of all MAPKs. Several kinases participate in activation of the ERK cascade. This cascade is initiated by the small G protein Ras, which upon stimulation causes activation Raf1 kinase. Raf1 continues the transmission by activating MEK. Activated MEK appears to be the only kinase capable of specifically phosphorylating and activating ERK. ERK appears to be an important regulatory molecule, which by can phosphorylate regulatory targets in the cytosol (phospholipase A2, PLA2), translocated into and phosphorylate substrates in the nucleus (ELK1). The activation of ERK cascade mediates and regulates the signal transduction pathways in response to stress, mitogenic signals and is important in development and differentiation, learning, memory and survival.
Immunogen: synthetic peptide HTGFLTEYVAT, corresponding to the non-phosphorylated form of ERK-activation loop.
Physical form: Solution in phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
Preparation Note: Prepared from a culture supernatant of bioreactor grown hybridoma
RIDADR NONH for all modes of transport
WGK Germany nwg
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Storage Temp. −20°C
UNSPSC 12352203

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