Mouse Monoclonal Tenascin C antibody. Suitable for WB, IHC-Fr and reacts with Human samples. Cited in 5 publications. Immunogen corresponding to Native Full Length Protein corresponding to Human TNC.
Preservative: 0.09% Sodium azide
Constituents: PBS, 1% BSA
WB | IHC-Fr | |
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Human | Tested | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
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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).
HXB, TNC, Tenascin, TN, Cytotactin, GMEM, GP 150-225, Glioma-associated-extracellular matrix antigen, Hexabrachion, JI, Myotendinous antigen, Neuronectin, Tenascin-C, TN-C
Mouse Monoclonal Tenascin C antibody. Suitable for WB, IHC-Fr and reacts with Human samples. Cited in 5 publications. Immunogen corresponding to Native Full Length Protein corresponding to Human TNC.
Preservative: 0.09% Sodium azide
Constituents: PBS, 1% BSA
ab88280 reacts with the 4th and 5th fibronectin repeats of human
Tenascin C polypeptides.
ab88280 is derived from the hybridoma produced by fusion between myeloma cells and Balb/c spleen cells.
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Tenascin C also known as hexabrachion is an extracellular matrix glycoprotein with a mass of approximately 220-300 kDa depending on post-translational modifications. It shows high expression in areas undergoing tissue remodeling such as embryonic tissues wounds and tumors. It consists of repeating structural elements including epidermal growth factor-like repeats and fibronectin type III domains which facilitate its function in the context of tissue dynamics.
The large hexamer known as Tenascin C plays a significant role in modulating cell adhesion migration and proliferation especially during developmental processes and injury responses. It incorporates into the existing extracellular matrix as a loose network which provides elasticity and supports cellular activities. This feature allows Tenascin C to interact with other matrix molecules and cell surface receptors to regulate tissue morphogenesis.
Tenascin C actively participates in the Wnt and TGF-beta signaling pathways important for controlling cellular behavior in development and regeneration. It associates with integrins and glycoproteins to influence cell responses to signaling events in these pathways. By modulating these interactions Tenascin C can impact processes such as epithelial-to-mesenchymal transition and angiogenesis affecting tissue architecture and function.
Tenascin C exhibits a strong connection to cancer progression and chronic inflammatory conditions such as rheumatoid arthritis. Its levels rise in tumors and inflamed tissues where it interacts with other matrix components and cytokines like interleukin-6 (IL-6). These interactions contribute to a microenvironment that promotes tumor growth and persistence of inflammation highlighting its role in the pathophysiology of these diseases.
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False colour image of Western blot: Anti-Tenascin C antibody [EB2] staining at 1/1000 dilution, shown in green; Rabbit anti-ACTN4 [EPR2533(2)] (Anti-alpha Actinin 4 antibody [EPR2533(2)] ab108198) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab88280 was shown to bind specifically to Tenascin C. A band was observed at 200/270 kDa in treated wild-type U-2 OS cell lysates with no signal observed at this size in TNC knockout cell line Human TNC (Tenascin C) knockout U-2 OS cell line ab262488 (knockout cell lysate ab263924). To generate this image, wild-type and TNC knockout U-2 OS cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 2 % BSA in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times before development with Optiblot (ECL reagent Anti-PKC delta (phospho S299) antibody [EPNCI119] ab133456) and imaged with 16 minutes exposure time. Secondary antibodies used were HRP conjugated Goat anti-Mouse (H+L) and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed (Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777) at 1/20000 dilution.
All lanes: Western blot - Anti-Tenascin C antibody [EB2] (ab88280) at 1/1000 dilution
Lane 1: Wild-type U-2 OS Treated BFA (5 ug/mL, 6 h) cell lysate at 40 µg
Lane 2: TNC knockout U-2 OS Treated BFA (5 ug/mL, 6 h) cell lysate at 40 µg
Lane 2: Western blot - Human TNC (Tenascin C) knockout U-2 OS cell line (Human TNC (Tenascin C) knockout U-2 OS cell line ab262488)
Lane 3: Wild-type U-2 OS Vehicle Control BFA (0 ug/mL, 6 h) cell lysate at 40 µg
Lane 4: TNC knockout U-2 OS Vehicle Control BFA (0 ug/mL, 6 h) cell lysate at 40 µg
Lane 5: U-87 MG Treated BFA (5ug/mL, 6h) cell lysate at 40 µg
Lane 6: U-87 MG cell lysate at 40 µg
Performed under reducing conditions.
Predicted band size: 241 kDa
Observed band size: 200 kDa, 270 kDa
ab88280, staining Tenascin C in vulva carcinoma frozen tissue sections by Immunohistochemistry.
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