Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P, IF-Tissue |
Clonality: | Monoclonal |
Clone number: | JE47-61 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. 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: 305 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human Thyroglobulin aa 2,620-2,768 / 2,768. |
Positive control: | Human thyroid gland tissue. |
Subcellular location: | Secreted. |
Recommended Dilutions:
WB IHC-P IF-Tissue |
1:500 1:1,000 1:200 |
Uniprot #: | SwissProt: P01266 Human |
Alternative names: | AITD 3 AITD3 hTG TDH3 Tg TGN THYG_HUMAN Thyroglobulin |
Fig1: Immunohistochemical analysis of paraffin-embedded human thyroid gland tissue using anti-Thyroglobulin antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET7109-64, 1/50) 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. | |
Fig2:
Immunohistochemical analysis of paraffin-embedded human thyroid cancer tissue with Rabbit anti-Thyroglobulin antibody (ET7109-64) at 1/1,000 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 (ET7109-64) at 1/1,000 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. |