Thyroglobulin Recombinant Rabbit Monoclonal Antibody [JE47-61]
cat.: ET7109-64
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P, IF-Tissue, IF-Cell
Clonality: Monoclonal
Clone number: JE47-61
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
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, human thyroid cancer tissue, TT.
Subcellular location: Secreted.
Recommended Dilutions:
  WB
  IHC-P
  IF-Tissue
  IF-Cell

1:500
1:1,000
1:200
1:100
Uniprot #: SwissProt: P01266 Human
Alternative names: AITD 3 AITD3 hTG TDH3 Tg TGN THYG_HUMAN Thyroglobulin
Images
ET7109-64_1.jpg 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.
ET7109-64_2.jpg 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.
ET7109-64_3.jpg Fig3: Immunocytochemistry analysis of TT cells labeling Thyroglobulin with Rabbit anti-Thyroglobulin antibody (ET7109-64) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Thyroglobulin antibody (ET7109-64) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (HA601187, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.