Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Multiclonal Caveolin-3 antibody. Carrier free. Suitable for IP, WB, IHC-P, ICC/IF, IHC-Fr, Flow Cyt (Intra) and reacts with Mouse, Rat, Human samples.
View Alternative Names
Caveolin-3, M-caveolin, CAV3
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized RD cells labelling Caveolin-3 with ab289544 at 1/100 (4.77 μg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 μg/mL) dilution (Green). Confocal image showing cytoplasmic staining in RD cell line. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5 μg/ml) dilution (Red). The nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 μg/mL) dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 0.1% Tween-20 permeabilized RD (Human muscle spindle cells and large multinucleated cells) cells labelling Caveolin-3 with ab289544 at 1/50 dilution (1 μg) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human kidney tissue labelling Caveolin-3 with ab289544 at 1/5000 (0.095 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The section was incubated with ab289544 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins.
Negative control : no staining on human kidney.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human cardiac muscle tissue labelling Caveolin-3 with ab289544 at 1/5000 (0.095 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Membranous staining on human cardiac muscle is observed. The section was incubated with ab289544 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins.
- IP
Supplier Data
Immunoprecipitation - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Caveolin-3 was immunoprecipitated from 0.35 mg human heart lysate 10 μg with ab289544 at 1/30 dilution (2 μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab289544 at 1/2000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/10000 dilution.
Lane 1 : Human heart lysate 10 μg
Lane 2 : ab289544 IP in human heart lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab289544 in human heart lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 8 seconds
All lanes:
Immunoprecipitation - Anti-Caveolin-3 antibody [RM1042] - Caveolae Marker (<a href='/en-us/products/primary-antibodies/caveolin-3-antibody-rm1042-caveolae-marker-ab289544'>ab289544</a>)
Predicted band size: 17 kDa
Observed band size: 17 kDa
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse kidney tissue labelling Caveolin-3 with ab289544 at 1/5000 (0.095 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The section was incubated with ab289544 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins.
Negative control : no staining on mouse kidney.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized C2C12 (Mouse myoblasts myoblast) differentiated to muscle for 7 days (Right) / Undifferentiated C2C12 cells (Left). Cells labelling Caveolin-3 with ab289544 at 1/500 dilution (0.1 μg)/ Left and Right. Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cardiac muscle tissue labelling Caveolin-3 with ab289544 at 1/5000 (0.095 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Membranous staining on rat cardiac muscle is observed. The section was incubated with ab289544 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cardiac muscle tissue labelling Caveolin-3 with ab289544 at 1/5000 (0.095 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Membranous staining on mouse cardiac muscle is observed. The section was incubated with ab289544 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat skeletal muscle (fresh) tissue labeling Caveolin-3 with ab289544 at 1/1000 (0.956 μg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 μg/mL) dilution (Green). Positive staining on rat skeletal muscle is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 μg/mL) dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse skeletal muscle (fresh) tissue labeling Caveolin-3 with ab289544 at 1/1000 (0.956 μg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 μg/mL) dilution (Green). Positive staining on mouse skeletal muscle is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 μg/mL) dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat kidney tissue labelling Caveolin-3 with ab289544 at 1/5000 (0.095 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The section was incubated with ab289544 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used.
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins.
Negative control : no staining on rat kidney.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized C2C12 cells labelling Caveolin-3 with ab289544 at 1/100 (4.77 μg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 μg/mL) dilution (Green). Confocal image showing cytoplasmic and membranous staining in differentiated C2C12 cells. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5 μg/ml) dilution (Red). The nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 μg/mL) dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Caveolin-3 was immunoprecipitated from 0.35 mg mouse heart lysate 10 μg with ab289544 at 1/30 dilution (2 μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab289544 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse heart lysate 10 μg
Lane 2 : ab289544 IP in mouse heart lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab289544 in mouse heart lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 seconds
Dimerized Caveolin-3 was observed at around 34kDa. (PMID : 21362625)
All lanes:
Immunoprecipitation - Anti-Caveolin-3 antibody [RM1042] - Caveolae Marker (<a href='/en-us/products/primary-antibodies/caveolin-3-antibody-rm1042-caveolae-marker-ab289544'>ab289544</a>)
Predicted band size: 17 kDa
Observed band size: 17 kDa
false
- IP
Supplier Data
Immunoprecipitation - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Caveolin-3 was immunoprecipitated from 0.35 mg rat heart lysate 10 μg with ab289544 at 1/30 dilution (2 μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab289544 at 1/2000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/10000 dilution.
Lane 1 : Rat heart lysate 10 μg
Lane 2 : ab289544 IP in rat heart lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab289544 in rat heart lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 8 seconds
Dimerized Caveolin-3 was observed at around 34kDa. (PMID : 21362625)
All lanes:
Immunoprecipitation - Anti-Caveolin-3 antibody [RM1042] - Caveolae Marker (<a href='/en-us/products/primary-antibodies/caveolin-3-antibody-rm1042-caveolae-marker-ab289544'>ab289544</a>)
Predicted band size: 17 kDa
false
- WB
Lab
Western blot - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Dimerized Caveolin-3 was observed at around 34kDa. (PMID : 21362625)
Exposure time : 100 seconds
All lanes:
Western blot - Anti-Caveolin-3 antibody [RM1042] - Caveolae Marker (<a href='/en-us/products/primary-antibodies/caveolin-3-antibody-rm1042-caveolae-marker-ab289544'>ab289544</a>) at 1/1000 dilution
Lane 1:
RD (Human muscle spindle cells and large multinucleated cells) whole cell lysate at 20 µg
Lane 2:
Human skeletal muscle lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/10000 dilution
Predicted band size: 17 kDa
Observed band size: 17 kDa
false
- WB
Lab
Western blot - Anti-Caveolin-3 antibody [RM1042] - BSA and Azide free (AB289555)
This data was developed using ab289544, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST **Negative control** : Kidney (PMID : 8567687). Higher molecular bands could be sumoylated Caveolin-3. (PMID : 21362625) Exposure time : 15 seconds
All lanes:
Western blot - Anti-Caveolin-3 antibody [RM1042] - Caveolae Marker (<a href='/en-us/products/primary-antibodies/caveolin-3-antibody-rm1042-caveolae-marker-ab289544'>ab289544</a>) at 1/1000 dilution
Lane 1:
C2C12 (Mouse myoblasts myoblast) whole cell lysate at 20 µg
Lane 2:
C2C12 differentiated to muscle for 7 days whole cell lysate at 20 µg
Lane 3:
Human heart lysate at 20 µg
Lane 4:
Human kidney lysate at 20 µg
Lane 5:
Mouse heart lysate at 20 µg
Lane 6:
Mouse kidney lysate at 20 µg
Lane 7:
Rat heart lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/5000 dilution
Predicted band size: 17 kDa
Observed band size: 17 kDa
false
Related conjugates and formulations (1)
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Anti-Caveolin-3 antibody [RM1042] - Caveolae Marker
Reactivity data
Product details
ab289555 is the carrier free version of ab289544.
What are recombinant multiclonals?
Recombinant multiclonals are a mixture of recombinant antibodies co-expressed from a library of heavy and light chains. They offer several advantages including:
- - The sensitivity of polyclonal antibodies by recognising multiple epitopes
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
View our range of recombinant multiclonal antibodies.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Caveolae perform vital functions in cellular signaling and endocytosis. Caveolin-3 assists in various signaling pathways within muscle cells and interacts with other caveolae markers to facilitate signal transduction. It often forms a complex with other caveolin proteins such as caveolin-1 creating an environment conducive for the embedding of signaling molecules. This protein also modulates the trafficking and function of certain ion channels and receptors impacting muscle physiology.
Pathways
Caveolin-3 significantly influences pathways concerned with muscle function and signal transduction. In particular it involves itself with the nitric oxide (NO) signaling pathway and beta-adrenergic signaling both critical to the contractile functions of muscle tissues. It closely interacts with proteins such as endothelial nitric oxide synthase (eNOS) and components of the G-protein coupled receptor family indicating its pivotal role in mediating physiological responses to stimuli.
Product protocols
- Visit the General protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com