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Mouse anti-TFF1/pS2, Clone: GE2, Azide Free, Novus Biologicals™


Manufacturer: novus biologicals canada  NBP23462301MG

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 Disclaimers

For Research Use Only

Catalog No. NBP23462301

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Description & Specifications

Specifications

Antigen TFF1/pS2
Host Species Mouse
Immunogen Synthetic peptide of 28 amino acid residues corresponding to CFDDTVRGVPWCFYPNTIDVPPEEECEF (aa57-84) from the C-terminus of human pS2.
Monoclonal or Polyclonal Monoclonal
Isotype IgG1, κ
Storage Requirements Store at -20 to -80°C. Avoid freeze-thaw cycles.
Reconstitution Protein A purified
Concentration 1mg/mL
Formulation 10mM PBS. Does not contain BSA. Azide Free.
Applications ELISA
Applications Flow Cytometry
Applications Immunocytochemistry
Applications Immunofluorescence
Applications Immunohistochemistry (Frozen)
Applications Immunohistochemistry (Paraffin)
Applications Immunoprecipitation
Applications Western Blotting
Quantity 0.1mg
Conjugate Unlabeled
Cross Reactivity Human
Cross Reactivity Primate
Format Purified
Gene Accession No. P04155
Purification Method Purified
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 7031
Test Specificity It recognizes a polypeptide of 6.5kDa, identified as pS2 estrogen-regulated protein. Its epitope is localized between aa57-84 of human pS2 protein. pS2 is a trefoil peptide. Trefoil peptides are protease resistant molecules secreted throughout the gut that play a role in mucosal healing. These peptides contain three intra-chain disulfide bonds, forming the trefoil motif, or P-domain. pS2 is known to form dimers and this dimerization is thought to play a role in its protective and healing properties. About 60% of breast carcinomas are positive for pS2. Staining is cytoplasmic, often with localization to the Golgi apparatus. pS2 is shown to be localized in normal stomach mucosa, gastric fluid, goblet cells in the colon and small intestine, and in ulcerations of the gastrointestinal tract. Several studies have shown that pS2 is primarily expressed in estrogen receptor-positive breast tumors and it may define a subset of estrogen-dependent tumors that displays an increased likelihood of response to endocrine therapy. Reacts to Cynomolgus Monkey.
Clone GE2