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| Product Name | ST14 antibody - Aminoterminal end cleaved protein |
| | See all ST14 antibodies (6)... |
| Product type | Primary antibodies |
| Description | Rabbit polyclonal to ST14 - Aminoterminal end cleaved protein |
| Immunogen | This antibody is made to a synthetic peptide based on the amino end of shed human ST14.(Peptide available as ab41265.) |
| Reacts with | Hu |
| Predicted to react (species key) | Ms, Rat (Due to sequence homology) |
| Specificity | Ab28265 reacts with ST14, and does not recognize matriptase2. We have a range of domain specific antibodies for this target. For a full list please see all ST14 antibodies |
| Tested applications (see key) | WB |
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| Application notes (see key) | Recommended dilutions WB: Use at an assay dependent dilution. Predicted molecular weight: 95 kDa. Nonreduced SDS-PAGE Western blots yield bands of 110-95 kDa for ST14 complexed with HAI1 and a 70 kDa band for the single-chain form. The 95 kDa complex resolves to A and B chains of 45 and 25 kDa for ST14, plus a 36 kDa band for the HAI1. The single-chain form is produced by cleavage in the SEA domain, between the stem and the CUB domains and the catalytic domain is liberated by cleavage after the LRLR domains. A recommended starting concentration for Western blots is 1/1,000 when using colorimetric substrates such as BCIP/NBT, and 1/5,000 for chemiluminescent substrates. Higher concentrations of antibody may be needed for samples from more distantly related species. EDTA/EGTA treatment of tissues or lysates is required to see latent zymogen. Dilution optimised using Chromogenic detection. Not yet tested in other applications. Optimal dilutions/concentrations should be determined by the end user. |
| Cellular localization | Membrane; single-pass type II membrane protein |
| Research areas | Cell Biology >> Proteolysis / Ubiquitin >> Proteolytic enzymes >> Serine protease >> Matriptase Cancer >> Invasion/microenvironment >> ECM >> Extracellular matrix >> Other Signal Transduction >> Cytoskeleton / ECM >> Extracellular Matrix >> ECM Enzymes >> Other Enzymes |
| Relevance | ST14 degrades extracellular matrix. It is proposed to play a role in breast cancer invasion and metastasis. ST14 was first identified as a gelatinolytic proteinase in the media and cell lysates of breast tumor cells in culture. Originally it was thought to be specific for either prostate tumors or breast tumors, or to be a tumor suppressor. More extensive characterizations determined that ST14 is found in many normal and tumor cell lines, and in breast milk, serum and urine. ST14 is a Type II serine proteinase, meaning it contains a transmembrane motif in the amino end of the protein. The latent protein is membrane attached, and has a cytoplasmic tail. The extracellular domains contain a stem region, followed by two CUB domains and four repeats of LDL receptor like homology, and a serine protease domain located in the carboxyterminal end of the protein. ST14 is a member of the S1A family of the PA clan of serine proteinases, which includes acrosin, kallikreins, trypsin, chymotrypsin, and many other important enzymes. |
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| Database links | The links below go to external sites and will open in a new browser window |
| Raised in | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Purity | Immunogen affinity purified |
| Storage buffer | Preservative: 0.05% Sodium Azide Constituents: 50% Glycerol Material safety datasheets (MSDS) for this product: Glycerol MSDS Sodium Azide MSDS
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| Form | Liquid |
| Concentration | 1.000 mg/ml |
| Storage instructions | Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles. |
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| Search PubMed (MEDLINE) for references to ST14 |
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