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Key Documents

SAB5600057

Sigma-Aldrich

Anti-p38 MAPK Phospho (pT180/pY182) antibody, Rabbit monoclonal

recombinant, expressed in HEK 293 cells, clone RM243, purified immunoglobulin

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

recombinante

expressed in HEK 293 cells

Nivel de calidad

forma del anticuerpo

purified immunoglobulin

tipo de anticuerpo

primary antibodies

clon

RM243, monoclonal
recombinant monoclonal

formulario

buffered aqueous glycerol solution

reactividad de especies

human

técnicas

immunoblotting: 1:1000-1:2000
immunohistochemistry: 1:500-1:1000

isotipo

IgG

Nº de acceso NCBI

Condiciones de envío

wet ice

temp. de almacenamiento

−20°C

modificación del objetivo postraduccional

phosphorylation (pThr180/pTyr182)

Información sobre el gen

human ... MAPK14(1432)

Descripción general

The mitogen activated protein kinase (MAPK) gene codes for a serine/threonine protein kinase which is found to be expressed in majority of cells. The MAPK gene is mapped to human chromosome 6p21.31 and the encoded protein consists of 90 to 360 amino acids residues. MAPKs are divided into three subtypes : extracellular signal-regulated kinases (ERK), c-Jun amino-terminal kinases (JNK) and p38 MAPK (p38).

Especificidad

This antibody reacts to p38 MAPK only when dual phosphorylation at Thr180 and Tyr182 is observed. There is no cross-reactivity with p38 MAPK without dual phosphorylation at Thr180 and Tyr182.

Inmunógeno

Synthetic phospho-peptide corresponding to human Phospho-p38 MAPK (Thr180/Tyr182)

Aplicación

Anti-p38 MAPK Phospho (pT180/pY182) antibody, Rabbit monoclonal has been used for immunodetection.

Acciones bioquímicas o fisiológicas

Mitogen activated protein kinase (MAPK) participates in transdifferentiation of adipocytes in myoblast by regulating adipogenic and adipolysis metabolism. p38 MAPK is associated with various biological processes as such as cell proliferation and differentiation, cell adhesion, migration. It mediates pro-apoptotic signal during apoptosis, contributing either to cell death or survival.. p38 MAPK is known to mediate a number of metabolic pathways by controlling transcription, mRNA stability, chromatin remodelling and protein synthesis. During initial process of tumorigenesis, It acts as a tumor suppressor, while it might promote metastasis in the later stages of the same. p38 MAPK gets activated in response to growth factors, oxidative stress, proinflammatory cytokines and DNA damage.

Características y beneficios

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Forma física

Solution in phosphate buffered saline containing 50% glycerol, 1% BSA and 0.09% sodium azide.

Cláusula de descargo de responsabilidad

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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Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

MAPK14 (mitogen-activated protein kinase 14).
Porras A and Guerrero Arroyo M D C
Atlas of Genetics and Cytogenetics in Oncology and Haematology (2011)
TINCR facilitates non-small cell lung cancer progression through BRAF-activated MAPK pathway.
Zhu Z J and He J K
Biochemical and Biophysical Research Communications, 497(4), 971-977 (2018)
Expressions and regulatory effects of P38/ERK/JNK MAPKs in the adipogenic trans-differentiation of C2C12 myoblasts.
Qi R, et al.
Cellular Physiology and Biochemistry, 44(6), 2467-2475 (2017)

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