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SMAD4 Polyclonal Antibody Storage Store at -20°C

SKU: E-AB-34159-200

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SMAD4 Polyclonal Antibody Storage Store at -20°C

 

SKU # E-AB-34159
Reactivity Human, Mouse, Rat, Monkey
Host Rabbit
Applications IHC-p, IF

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse, Rat, Monkey
Applications IHC-p,  IF
Clonality Polyclonal
Immunogen Synthesized peptide derived from the N-terminal region of human Smad4
Abbre SMAD4
Synonyms (Small) Mothers Against Decapentaplegic,  DPC 4,  DPC4,  Deleted in Pancreatic Carcinoma,  Deleted in Pancreatic Carcinoma 4,  Deleted in pancreatic carcinoma locus 4,  Deletion target in pancreatic carcinoma 4,  JIP,  MAD homolog 4,  MAD mothers against decapentapl,  hSMAD4
Swissprot
Calculated MW 60 kDa
Observed MW 60 kDa

Cellular Localization Cytoplasm. Nucleus. Cytoplasmic in the absence of ligand. Migrates to the nucleus when complexed with R-SMAD.
Concentration 1 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 0.5% protein protectant and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Cardiovascular,  Epigenetics and Nuclear Signaling,  Metabolism,  Signal Transduction,  Stem Cells
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
WB 1:100-1:300
IHC 1:200-1:1000

 

Background

This gene encodes a member of the Smad family of signal transduction proteins. Smad proteins are phosphorylated and activated by transmembrane serine-threonine receptor kinases in response to TGF-beta signaling. The product of this gene forms homomeric complexes and heteromeric complexes with other activated Smad proteins, which then accumulate in the nucleus and regulate the transcription of target genes. This protein binds to DNA and recognizes an 8-bp palindromic sequence (GTCTAGAC) called the Smad-binding element (SBE). The Smad proteins are subject to complex regulation by post-translational modifications. Mutations or deletions in this gene have been shown to result in pancreatic cancer, juvenile polyposis syndrome, and hereditary hemorrhagic telangiectasia syndrome. SMAD4 (SMAD Family Member 4) is a Protein Coding gene. Diseases associated with SMAD4 include Myhre Syndrome and Polyposis, Juvenile Intestinal. Among its related pathways are PEDF Induced Signaling and Validated targets of C-MYC transcriptional repression. GO annotations related to this gene include transcription factor activity, sequence-specific DNA binding and sequence-specific DNA binding. An important paralog of this gene is SMAD9.