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Recombinant Human SMAD4 Protein (His Tag)

Uniprot : Q13485
  • Cat.No.:PKSH033066

  • Expression host: E.coli

To Purchase PKSH033066

Size:
  • 10μg
  • 50μg
Price: $130
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Description

Synonyms Mothers Against Decapentaplegic Homolog 4;MAD Homolog 4;Mothers Against DPP Homolog 4;Deletion Target in Pancreatic Carcinoma 4;SMAD Family Member 4;SMAD 4;Smad4;hSMAD4;SMAD4;DPC4;MADH4
Species Human
Expression_host E.coli
Sequence Met 1-Asp552
Accession Q13485
Mol_Mass 61.5 kDa
AP_Mol_Mass 62 kDa
Tag C-His

Properties

Purity > 80 % as determined by reducing SDS-PAGE.
Endotoxin level < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from a 0.2 μm filtered solution of 20mM Tris-HCl, pH 8.0.
Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.

Background

SMAD Family Member 4 (SMAD4) is a cytoplasmic protein that belongs to the Dwarfin/SMAD family. SMAD4 contains one MH1 (MAD homology 1) domain and one MH2 (MAD homology 2) domain. It is the component of the heterotrimeric SMAD2/SMAD3-SMAD4 complex that forms in the nucleus and is required for the TGF-mediated signaling. SMAD4 promotes binding of the SMAD2/SMAD4/FAST-1 complex to DNA and provides an activation function required for SMAD1 or SMAD2 to stimulate transcription. SMAD4 may act as a tumor suppressor. It positively regulates PDPK1 kinase activity by stimulating its dissociation from the 14-3-3 protein YWHAQ which acts as a negative regulator. Mutations or deletions in SMAD4 have been shown to result in pancreatic cancer, juvenile polyposis syndrome, and hereditary hemorrhagic telangiectasia syndrome.

Citations

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