SMADs are members of the MAD-related family of molecules. MAD-related proteins are a family of intracellular proteins that are essential components in the signaling pathways of the serine/threonine kinase receptors of the transforming growth factor beta superfamily. Alterations in the SMAD4 gene was primarily discovered in pancreatic cancer (duct adenocarcinoma) but occur in a variety of cancers such as colorectal cancer, gastric cancer, prostate cancer, melanomas, head and neck cancers and many others, though with higher frequencies in gastrointestinal tract cancers. Loss of SMAD4 expression in tumors has also been shown to affect cancer progression and therapy, such as reduced response to adjuvant chemotherapy.
Smad4
Catalog No: RP173-
Categories: Primary Antibodies, IVD - For U.S. Market, IVD - Outside U.S. Market
Tags: S, Concentrated, Ready to Use
Description
Additional information
Catalog No. | PDR173 Prediluted, RP173 Concentrated |
---|---|
Clone | Rabbit |
Immunogen | Recombinant fragment corresponding to a region within amino acids 322 and 552 of SMAD4 |
Species | Rabbit |
Cellular Localization | Nuclear/Cytoplasm |
Positive Control Tissue | Colon Ca, Pancreas Ca |
Pretreatment | EDTA (pH 8.0) |
Incubation & Temperature | 30 min @ RT |
Intended Use | IVD |
Detection System | PolyVue Plus – Two Step Detection System or Montage PolyVue Plus Auto Detection System for Montage 360 System |
Description/Type | Rabbit Polyclonal Antibody |
Format | Purified immunoglobulin fraction ofrabbit antiserum containing sodium azide as a preservative. |
DATASHEETS & SDS
DATASHEETS & SDS
Download Datasheet |
Download SDS Sheet – OSHA |
REFERENCES
REFERENCES
- Shi S et al. Metabolic tumor burden is associated with major oncogenomic alterations and serum tumor markers in patients with resected pancreatic cancer. Cancer Lett 360:227-33 (2015). IHC ; Human
- Shi Y, et.al. A structural basis for mutational inactivation of the tumour suppressor Smad4. Nature. 1997;388:87–93.The first crystal structure of a Smad domain, the Smad4 MH2.
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