Tenascin C Recombinant Rabbit Monoclonal Antibody [SU36-01]
cat.: ET1608-50
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
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
Images
ET1608-50_1.jpg 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.
ET1608-50_2.jpg 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).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.