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Smad3 (Phospho-Ser213) Rabbit pAb

Smad3 (Phospho-Ser213) Rabbit pAb

ENT-A8219

Description

 

 

 

REF ENT-A8219
Category Antibody Polyclonal
Description Smad3 (Phospho-Ser213) Rabbit pAb
Source Rabbit
Applications WB;ELISA;IHC
Reactivity Human;Mouse;Rat
Reactivity Human;Mouse;Rat
Dilution WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
Immunogen Synthesized phospho derived from human Smad3 (Phospho-Ser213)
Storage Stability -20°C/1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band KD 50kD
Human Gene ID 4088
Human Swiss Prot Nº P84022
Subcellular Location Cytoplasm . Nucleus . Cytoplasmic and nuclear in the absence of TGF-beta. On TGF-beta stimulation, migrates to the nucleus when complexed with SMAD4 (PubMed:15799969, PubMed:21145499). Through the action of the phosphatase PPM1A, released from the SMAD2/SMAD4 complex, and exported out of the nucleus by interaction with RANBP1 (PubMed:16751101, PubMed:19289081). Co-localizes with LEMD3 at the nucleus inner membrane (PubMed:15601644). MAPK-mediated phosphorylation appears to have no effect on nuclear import (PubMed:19218245). PDPK1 prevents its nuclear translocation in response to TGF-beta (PubMed:17327236). Localized mainly to the nucleus in the early stages of embryo development with expression becoming evident in the cytoplasm of the inner cell mass at the blastocyst stage (By similarity)

Other Name: Mothers against decapentaplegic homolog 3 (MAD homolog 3) (Mad3) (Mothers against DPP homolog 3) (hMAD-3) (JV15-2) (SMAD family member 3) (SMAD 3) (Smad3) (hSMAD3)

Background: The protein encoded by this gene belongs to the SMAD, a family of proteins similar to the gene products of the Drosophila gene ‘mothers against decapentaplegic’ (Mad) and the C. elegans gene Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein functions as a transcriptional modulator activated by transforming growth factor-beta and is thought to play a role in the regulation of carcinogenesis. [provided by RefSeq, Apr 2009],