Tenascin C (Stromal Marker For Epithelial Malignancy) Antibody - With BSA and Azide
Mouse Monoclonal Antibody [Clone SPM319 ]
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Application ![]()
| IHC, IF, FC |
---|---|
Primary Accession | P24821 |
Other Accession | 3371, 143250 |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Isotype | Mouse / IgG1, kappa |
Clone Names | SPM319 |
Calculated MW | 240853 Da |
Gene ID | 3371 |
---|---|
Other Names | Tenascin, TN, Cytotactin, GMEM, GP 150-225, Glioma-associated-extracellular matrix antigen, Hexabrachion, JI, Myotendinous antigen, Neuronectin, Tenascin-C, TN-C, TNC, HXB |
Application Note | IHC~~1:100~500 IF~~1:50~200 FC~~1:10~50 |
Storage | Store at 2 to 8°C.Antibody is stable for 24 months. |
Precautions | Tenascin C (Stromal Marker For Epithelial Malignancy) Antibody - With BSA and Azide is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | TNC |
---|---|
Synonyms | HXB |
Function | Extracellular matrix protein implicated in guidance of migrating neurons as well as axons during development, synaptic plasticity as well as neuronal regeneration. Promotes neurite outgrowth from cortical neurons grown on a monolayer of astrocytes. Ligand for integrins alpha-8/beta-1, alpha-9/beta-1, alpha-V/beta-3 and alpha- V/beta-6. In tumors, stimulates angiogenesis by elongation, migration and sprouting of endothelial cells (PubMed:19884327). |
Cellular Location | Secreted, extracellular space, extracellular matrix |
Tissue Location | Detected in fibroblasts (at protein level). |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
In Western blotting, it reacts with two bands of ~MW of 210kDa and 300kDa, identified as two isoforms of Tenascin C. Specificity of this MAb is validated by sequential immunoprecipitation with a PAb against Tenascin C. Tenascin C is a multifunctional, disulfide-linkedĀhexameric extracellular matrix glycoprotein expressed in association with mesenchymal epithelial interactions during development and in the neo-vasculature and stroma of undifferentiated tumors. In adults, it is restricted to certain epithelial-stromal interfaces and increases markedly in hyper-proliferative diseases and in stroma of many neoplasms, including gliomas, breast, squamous and lung carcinomas.
REFERENCES
Verstraeten AA, et. al. British Journal of Dermatology, 1992, 127(6):571-4. |

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