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FCMAB100P

Sigma-Aldrich

Milli-Mark Anti-Phospho-Erk1/2 Antibody (Thr202/Tyr204, Thr185/Tyr187)-PE

clone AW39R, Milli-Mark®, from rabbit

Synonyme(s) :

Erk1

Erk2

p44-MAPK

p42-MAPK

MAPK2

PRKM2

p41mapk

PRKM1

p44

ERK2

P42MAPK

ERK

p42

MAPK1

ERT1

ERT2

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

rabbit

Niveau de qualité

Conjugué

PE

Forme d'anticorps

purified antibody

Type de produit anticorps

primary antibodies

Clone

AW39R, monoclonal

Espèces réactives

mouse, rat

Réactivité de l'espèce (prédite par homologie)

human (based on 100% sequence homology)

Fabricant/nom de marque

Milli-Mark®

Technique(s)

flow cytometry: suitable
western blot: suitable

Isotype

IgG

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

wet ice

Modification post-traductionnelle de la cible

phosphorylation ((pThr202/pTyr204), (pThr185/pTyr187))

Informations sur le gène

human ... MAPK3(5595)

Description générale

Erk (Extracellular signal-Related Kinase) is a family of two, highly homologous proteins denoted as Erk1 (p44, MAPK3) and Erk2 (p42, MAPK1) that both function in the same pathway. The two proteins are often referred to collectively as Erk1/2 or p44/p42 MAP kinase. The Erk pathway is considered the classical, canonical MAPK (Mitogen-Activated Protein Kinase) signaling pathway. It is an evolutionarily conserved pathway that controls and is a critical regulator of the growth and survival through the promotion of cell proliferation and the prevention of apoptosis. Erk is involved in the control of many fundamental cellular processes including cell proliferation, survival, differentiation, apoptosis, motility and metabolism. Erk is activated by growth factor stimulation of receptor tyrosine kinases (RTKs), GPCR, and/or integrin stimulation. This activates the Ras-Raf-MEK-Erk pathway that results in the phosphorylation/activation of Erk1/2 (p44/p42) on the TxY motif (Thr202/Tyr204 and Thr185/Tyr187 for Erk1 & Erk2, respectively).

Spécificité

Antibody recognizes Recognizes Erk 1 & 2 only when dually phosphorylated on its TxY activation motif.

Immunogène

Epitope: Phosphorylated Thr185/Phosphorylated Tyr187
Phosphorylated recombinant peptide corresponding to amino acids surrounding the pTEpY motif in the activation loop of human phospho-Erk1/2, in which the Thr and Tyr residues are phosphorylated

Application

Research Category
Signaling
Research Sub Category
MAP Kinases
This Milli-Mark Phospho-Erk1/2 antibody is validated for use in Flow & WB for the detection of the Milli-Mark Phospho-Erk1/2 protein.

Qualité

Evaluated by Flow Cytometry with Jurkat cells.

Description de la cible

42kDa and 44kDa Observed

Forme physique

Protein A purified
Purified Rabbit monoclonal supernatant conjugated to phycoerythrin in buffer containing PBS with 0.05% sodium azide

Stockage et stabilité

Stable for 6 months at 2-8°C from date of receipt. Protect from light.

Remarque sur l'analyse

Control
Jurkat Cells

Informations légales

MILLI-MARK is a registered trademark of Merck KGaA, Darmstadt, Germany

Clause de non-responsabilité

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.

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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Kai-Jie Fan et al.
Molecular medicine reports, 16(6), 9758-9762 (2017-10-19)
In the present study, the effects of dihydromyricetin on the proliferative potential of fibroblasts and lung carcinoma cells were investigated. Markedly higher expression levels of smooth muscle actin and platelet derived growth factors (PDGFs) were observed in the fibroblasts using

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