KSP Cadherin antibody

• Catalog Number: orb705574
• Category: Antibodies
• Description: Mouse monoclonal antibody to KSP Cadherin
• Species/Host: Mouse
• Clonality: Monoclonal
• Tested applications: IH
• Reactivity: Human
• Immunogen: KLH-conjugated synthetic peptide encompassing a sequence within human KSP Cadherin. The exact sequence is proprietary.
• Dilution range: IHC-P: 1:100-1:300
• Form/Appearance: Mouse IgG2a. Liquid in PBS containing 50% glycerol, 0.2% rAlbumin and 0.01% sodium azide.
• Conjugation: Unconjugated
• Target: CDH16
• Entrez: 1014
• UniProt ID: O75309
• Source: Mouse
• Storage: Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
• Buffer/Preservatives: Mouse IgG2a. Liquid in PBS containing 50% glycerol, 0.2% rAlbumin and 0.01% sodium azide.
• Alternative names: Anti-Cadherin-16 antibody, anti-Kidney-specific ca
• Note: For research use only
• Expiration Date: 12 months from date of receipt.

Immunohistochemical analysis of KSP Cadherin staining in human chromophobe cell renal carcinoma formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunohistochemical analysis of KSP Cadherin staining in human kidney formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunohistochemical analysis of KSP Cadherin staining in human renal clear cell carcinoma formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.