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Merck
CN

FCMAB100P

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

clone AW39R, Milli-Mark®, from rabbit

别名:

Erk1

Erk2

p44-MAPK

p42-MAPK

MAPK2

PRKM2

p41mapk

PRKM1

p44

ERK2

P42MAPK

ERK

p42

MAPK1

ERT1

ERT2

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
PE
Clone:
AW39R, monoclonal
Application:
flow cytometry
western blot
Species reactivity:
mouse, rat
Citations:
1
Technique(s):
flow cytometry: suitable
western blot: suitable
Uniprot accession no.:
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产品名称

Milli-Mark Anti-Phospho-Erk1/2 Antibody (Thr202/Tyr204, Thr185/Tyr187)-PE, clone AW39R, Milli-Mark®, from rabbit

biological source

rabbit

conjugate

PE

antibody form

purified antibody

antibody product type

primary antibodies

clone

AW39R, monoclonal

species reactivity

mouse, rat

species reactivity (predicted by homology)

human (based on 100% sequence homology)

manufacturer/tradename

Milli-Mark®

technique(s)

flow cytometry: suitable
western blot: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

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

Quality Level

Gene Information

human ... MAPK3(5595)

Analysis Note

Control
Jurkat Cells
Evaluated by Flow Cytometry with Jurkat cells.

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.

Biochem/physiol Actions

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

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

42kDa and 44kDa Observed
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).

Immunogen

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

Physical form

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

Preparation Note

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

Legal Information

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

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存储类别

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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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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