CD5 antibody

• Catalog Number: orb705488
• Category: Antibodies
• Description: Mouse monoclonal antibody to CD5
• Species/Host: Mouse
• Clonality: Monoclonal
• Tested applications: IH
• Reactivity: Human
• Immunogen: KLH-conjugated synthetic peptide encompassing a sequence within human CD5. The exact sequence is proprietary.
• Dilution range: IHC-P: 1:100-1:300
• Form/Appearance: Mouse IgG. Liquid in PBS containing 50% glycerol, 0.2% rAlbumin and 0.01% sodium azide.
• Conjugation: Unconjugated
• Target: CD5
• Entrez: 921
• UniProt ID: P06127
• 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 IgG. Liquid in PBS containing 50% glycerol, 0.2% rAlbumin and 0.01% sodium azide.
• Alternative names: Anti-LEU1 antibody, anti-T-cell surface glycoprote
• Note: For research use only
• Expiration Date: 12 months from date of receipt.

Immunohistochemical analysis of CD5 staining in human classical hodgkin's lymphoma 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 CD5 staining in human tonsil 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 CD5 staining in human breast 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.