Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IP, IHC-P |
Clonality: | Monoclonal |
Clone number: | SY22-06 |
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: | 17 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human Caveolin-3 aa 1-125 / 151. |
Positive control: | Mouse heart tissue lysate, mouse skeletal muscle tissue lysate, rat heart tissue, human striated muscle tissue. |
Subcellular location: | Golgi apparatus membrane, Cell membrane, Membrane. |
Recommended Dilutions:
WB IHC-P |
1:1,000-1:5,000 1:1,000 |
Uniprot #: | SwissProt: P56539 Human | P51637 Mouse | P51638 Rat |
Alternative names: | CAV3 CAV3_HUMAN Caveolin 3 Caveolin-3 LGMD1C LQT9 M-caveolin MGC126100 MGC126101 MGC126129 OTTHUMP00000115603 OTTHUMP00000207105 VIP 21 VIP21 |
Fig1:
Western blot analysis of Caveolin-3 on different lysates using anti-Caveolin-3 antibody at 1/1,000 dilution. Positive control: Lane 1: Mouse heart tissue lysates Lane 2: Mouse skeletal muscle tissue lysates |
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Fig2:
Immunohistochemical analysis of paraffin-embedded rat heart tissue with Rabbit anti-Caveolin-3 antibody (ET1607-16) 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 (ET1607-16) 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. |
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Fig3:
Immunohistochemical analysis of paraffin-embedded human striated muscle tissue with Rabbit anti-Caveolin-3 antibody (ET1607-16) 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 (ET1607-16) 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. |