Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P, FC |
Clonality: | Monoclonal |
Clone number: | SU36-01 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 241 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human Tenascin C aa 2,152-2,201 / 2,201. |
Positive control: | Human tonsil tissue, SH-SY5Y. |
Subcellular location: | Extracellular matrix. |
Recommended Dilutions:
WB IHC-P FC |
1:500-1:1,000 1:50-1:400 1:50-1:100 |
Uniprot #: | SwissProt: P24821 Human |
Alternative names: | 150 225 Cytotactin Glioma associated extracellular matrix antigen Glioma-associated-extracellular matrix antigen GMEM GP 150 225 GP 150-225 GP Hexabrachion HXB JI MGC167029 Miotendinous antigen Myotendinous antigen Neuronectin TENA_HUMAN Tenascin Tenascin-C Tenascin-C isoform 14/AD1/16 TenascinC TN TN C TN-C TNC |
Fig1:
Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-Tenascin C antibody (ET1608-50) at 1/400 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1608-50) at 1/400 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig2: Flow cytometric analysis of Tenascin C was done on SH-SY5Y cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1608-50, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |