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KD-Validated Caveolin 3 Recombinant Rabbit mAb

#61345

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using Caveolin 3 antibody (Cat#61345). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using caveolin 3 antibody (Cat#61345). Caveolin 3 expression in wild type (WT) and caveolin 3 (CAV3) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using caveolin 3 antibody (Cat#61345). Total lysates (30 μg) from H9c2 cells and mouse heart tissue were loaded and separated by SDS-PAGE. The blot was incubated with caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunohistochemistry was performed on paraffin-embedded mouse skeletal muscle using caveolin 3 antibody (Cat#61345, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunohistochemistry was performed on paraffin-embedded mouse heart using caveolin 3 antibody (Cat#61345, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunocytochemical staining of HT-1080 cells with Caveolin 3 antibody (Cat#61345, 1:1,000). Nuclei were stained blue with DAPI; Caveolin 3 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of Caveolin 3 expression in C2C12 cells using Caveolin 3 antibody (Cat#61345, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Caveolin 3.
Please select the specifications of the product.
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Unit price:
$89.00
Quantity:
1
(Excluding sales tax)
  • Gene Symbol:
    CAV3
  • Catalog:
    61345
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H, M, R
Information
Product Name KD-Validated Caveolin 3 Recombinant Rabbit mAb
Aliases CAV3; Caveolin 3; M-Caveolin; VIP-21; LGMD1C; VIP21; LQT9; Caveolin-3; Cavolin 3; MPDT; RMD2
Background

Gene Name: CAV3

NCBI Gene Entry: 859

UniProt Entry: P56539

Application Information

Molecular Weight: Predicted, 17 kDa; observed, 20, 36 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB3035

Species Reactivity: Human, mouse, rat

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (ICC), immunohistochemistry-paraffin (IHC-P)

Immunogen A synthesized peptide derived from Caveolin-3
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage Store at -20 °C for one year.
Recommended Dilutions Western Blotting (WB): 1:1,000-1:5,000
Flow Cytometry (FCM): 1:200-1:2,000
Immunocytochemistry (ICC): 1:100-1:1,000
Immunohistochemistry-Paraffin (IHC-P): 1:100-1:200
Note This product is for research use only.
Data
  • Western blotting analysis using Caveolin 3 antibody (Cat#61345). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Western blotting analysis using caveolin 3 antibody (Cat#61345). Caveolin 3 expression in wild type (WT) and caveolin 3 (CAV3) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Western blotting analysis using caveolin 3 antibody (Cat#61345). Total lysates (30 μg) from H9c2 cells and mouse heart tissue were loaded and separated by SDS-PAGE. The blot was incubated with caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
  • Immunohistochemistry was performed on paraffin-embedded mouse skeletal muscle using caveolin 3 antibody (Cat#61345, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
  • Immunohistochemistry was performed on paraffin-embedded mouse heart using caveolin 3 antibody (Cat#61345, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
  • Immunocytochemical staining of HT-1080 cells with Caveolin 3 antibody (Cat#61345, 1:1,000). Nuclei were stained blue with DAPI; Caveolin 3 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
  • Flow cytometric analysis of Caveolin 3 expression in C2C12 cells using Caveolin 3 antibody (Cat#61345, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Caveolin 3.
Western blotting analysis using Caveolin 3 antibody (Cat#61345). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using caveolin 3 antibody (Cat#61345). Caveolin 3 expression in wild type (WT) and caveolin 3 (CAV3) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using caveolin 3 antibody (Cat#61345). Total lysates (30 μg) from H9c2 cells and mouse heart tissue were loaded and separated by SDS-PAGE. The blot was incubated with caveolin 3 antibody (Cat#61345, 1:5,000) and HRP-conjugated goat anti rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunohistochemistry was performed on paraffin-embedded mouse skeletal muscle using caveolin 3 antibody (Cat#61345, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunohistochemistry was performed on paraffin-embedded mouse heart using caveolin 3 antibody (Cat#61345, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunocytochemical staining of HT-1080 cells with Caveolin 3 antibody (Cat#61345, 1:1,000). Nuclei were stained blue with DAPI; Caveolin 3 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of Caveolin 3 expression in C2C12 cells using Caveolin 3 antibody (Cat#61345, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Caveolin 3.
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