H Cadherin Recombinant Rabbit Monoclonal Antibody [JB14-48]
cat.: ET7107-76
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: IHC-P, WB
Clonality: Monoclonal
Clone number: JB14-48
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: 78 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human H Cadherin aa 81-220 / 713.
Positive control: Human colon carcinoma tissue, human kidney tissue, rat skeletal muscle tissue, mouse heart tissue.
Subcellular location: Cell membrane, Membrane.
Recommended Dilutions:
  IHC-P
  WB

1:50-1:1,000
1:500
Uniprot #: SwissProt: P55290 Human | Q9WTR5 Mouse | Q8R490 Rat
Alternative names: CAD13_HUMAN Cadherin-13 CDH13 CDHH H-cadherin Heart cadherin P105 T cad T Cadherin T-cad T-cadherin Truncated cadherin
Images
ET7107-76_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue with Rabbit anti-H Cadherin antibody (ET7107-76) at 1/200 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 (ET7107-76) at 1/200 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.
ET7107-76_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-H Cadherin antibody (ET7107-76) at 1/200 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 (ET7107-76) at 1/200 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.
ET7107-76_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat skeletal muscle tissue with Rabbit anti-H Cadherin antibody (ET7107-76) at 1/200 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 (ET7107-76) at 1/200 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.
ET7107-76_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse heart tissue with Rabbit anti-H Cadherin antibody (ET7107-76) 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 (ET7107-76) 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.