N Cadherin Recombinant Antibody [SY02-46] - Mouse IgG1 (Chimeric) - BSA and Azide free
cat.: HA610298
| Product Type: | Recombinant Chimeric Antibody, primary antibodies |
|---|---|
| Species reactivity: | Human, Mouse, Rat |
| Applications: | IHC-Fr, IHC-P |
| Clone number: | SY02-46 |
| Form: | Liquid |
| Storage condition: | Store at 2-8℃. Avoid freeze. |
| Storage buffer: | 1*PBS (pH7.4). |
| Concentration: | 1ug/ul |
| Purification: | Protein A affinity purified. |
| Molecular weight: | Predicted band size: 100 kDa |
| Immunogen: | Synthetic peptide within Human N Cadherin aa 161-210 / 906. |
| Positive control: | Human liver tissue, mouse liver tissue, rat liver tissue. |
| Subcellular location: | Cell membrane. |
| Uniprot #: | SwissProt: P19022 Human | P15116 Mouse | Q9Z1Y3 Rat |
| Alternative names: | CADH2_HUMAN Cadherin 2 Cadherin 2 N cadherin neuronal Cadherin 2 type 1 Cadherin 2 type 1 N cadherin neuronal Cadherin 2, type 1, N-cadherin (neuronal) Cadherin-2 Cadherin2 Calcium dependent adhesion protein neuronal CD325 CD325 antigen CDH2 CDHN CDw325 CDw325 antigen N cadherin 1 N-cadherin NCAD Neural cadherin OTTHUMP00000066304 OTTHUMP00000067378 |
Images
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Fig1:
This data was developed using HA610298, the same antibody clone in a different buffer formulation. Application: IHC-Fr Species: Mouse Site: liver Sample: Frozen section Antibody concentration: 1/500 Antigen retrieval: Not required |
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Fig2:
This data was developed using HA610298, the same antibody clone in a different buffer formulation. Application: IHC-Fr Species: Rat Site: liver Sample: Frozen section Antibody concentration: 1/500 Antigen retrieval: Not required |
|
Fig3:
This data was developed using HA610298, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded human liver tissue with Mouse anti-N Cadherin antibody (HA610298) at 1/5,000 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 (HA610298) at 1/5,000 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. |
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Fig4:
This data was developed using HA610298, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Mouse anti-N Cadherin antibody (HA610298) at 1/5,000 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 (HA610298) at 1/5,000 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. |
|
Fig5:
This data was developed using HA610298, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded rat liver tissue with Mouse anti-N Cadherin antibody (HA610298) at 1/5,000 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 (HA610298) at 1/5,000 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”.