Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P, FC |
Clonality: | Monoclonal |
Clone number: | JM43-26 |
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: 77 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human PKC beta 1 aa 608-657 / 671. |
Positive control: | L929 cell lysates, human tonsil tissue, human spleen tissue, mouse kidney tissue, K562. |
Subcellular location: | Cytoplasm. Nucleus. Membrane. |
Recommended Dilutions:
WB IHC-P FC |
1:500 1:50-1:200 1:50-1:100 |
Uniprot #: | SwissProt: P05771 Human | P68404 Mouse | P68403 Rat |
Alternative names: | BTN6 BTNL11 MGC26137 MOG alpha 5 MOG alpha 6 MOG AluA MOG AluB MOG MOG Ig AluB MOG_HUMAN MOGIG2 Myelin oligodendrocyte glycoprotein Myelin-oligodendrocyte glycoprotein NRCLP7 |
Fig1:
Western blot analysis of PKC beta 1 on L929 cell lysates with Rabbit anti-PKC beta 1 antibody (ET1705-30) at 1/500 dilution. Lysates/proteins at 10 µg/Lane. Predicted band size: 77 kDa Observed band size: 77 kDa Exposure time: 2 minutes; 10% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1705-30) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature. |
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Fig2: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-PKC beta 1 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-30, 1/50) for 30 minutes 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. | |
Fig3: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-PKC beta 1 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-30, 1/50) for 30 minutes 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. |
Fig4: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-PKC beta 1 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-30, 1/50) for 30 minutes 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: Flow cytometric analysis of PKC beta 1 was done on K562 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1705-30, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |