Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal Sarcomeric Alpha Actinin antibody. Carrier free. Suitable for Dot, IHC-P, ICC/IF, WB and reacts with Recombinant full length protein - Human, Mouse, Rat, Human samples.
View Alternative Names
Alpha-actinin-2, Alpha-actinin skeletal muscle isoform 2, F-actin cross-linking protein, ACTN2
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized RD (human muscle multinucleated spindle-shaped cell) cells labelling Sarcomeric Alpha Actinin with ab317695 at 1/500 (1.05 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing cytoplasmic and membranous staining in RD cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labeled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5 ug/ml dilution (Magenta). 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 ug/ml dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labeling Sarcomeric Alpha Actinin with ab317695 at 1/100 (5.25 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse skeletal muscle. The section was incubated with ab317695 for 30 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 a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse primary cardiomyocyte cells labelling Sarcomeric Alpha Actinin with ab317695 at 1/500 (1.05 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing positive staining in mouse primary cardiomyocytes (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab9465 Anti-Sarcomeric Alpha Actinin mouse monoclonal antibody was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1 : ab317695 at 1/500 dilution, followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) antibody at 1/1000 dilution.
-ve control 2 : ab9465 at 1/500 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cardiac muscle tissue labeling Sarcomeric Alpha Actinin with ab317695 at 1/100 (5.25 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat cardiac muscle. The section was incubated with ab317695 for 30 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 a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat skeletal muscle tissue labeling Sarcomeric Alpha Actinin with ab317695 at 1/100 (5.25 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat skeletal muscle. The section was incubated with ab317695 for 30 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 a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized C2C12 (mouse myoblast) cells labelling Sarcomeric Alpha Actinin with ab317695 at 1/500 (1.05 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing cytoplasmic and membranous staining in differentiated C2C12 cells (shown in green). The counterstain was observed in magenta. Nuclear DNA was labeled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). 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 ug/ml dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling Sarcomeric Alpha Actinin with ab317695 at 1/100 (5.25 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse liver. The section was incubated with ab317695 for 30 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 a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling Sarcomeric Alpha Actinin with ab317695 at 1/100 (5.25 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on rat liver. The section was incubated with ab317695 for 30 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 a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized rat primary cardiomyocyte cells labelling Sarcomeric Alpha Actinin with ab317695 at 1/500 (1.05 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing positive staining in rat primary cardiomyocytes (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab9465 Anti-Sarcomeric Alpha Actinin mouse monoclonal antibody was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1 : ab317695 at 1/500 dilution, followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) antibody at 1/1000 dilution.
-ve control 2 : ab9465 at 1/500 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution.
- WB
Supplier Data
Western blot - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Negative control : liver, pancreas, placenta (PMID : 11440986).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] (<a href='/en-us/products/primary-antibodies/sarcomeric-alpha-actinin-antibody-epr28776-83-ab317695'>ab317695</a>) at 1/1000 dilution
Lane 1:
Human heart tissue lysate at 20 µg
Lane 2:
Human skeletal muscle tissue lysate at 50 µg
Lane 3:
Human liver tissue lysate at 50 µg
Lane 4:
Human pancreas tissue lysate at 50 µg
Lane 5:
Human placenta tissue lysate at 50 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 103 kDa,36 kDa
false
Exposure time: 180s
- Dot
Supplier Data
Dot Blot - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Dot blot analysis of Sarcomeric Alpha Actinin using ab317695 at 1 : 1000 (0.525 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Lane 1 : His-tagged human ACTN2 recombinant protein
Lane 2 : His-tagged human ACTN4 recombinant protein
Lane 3 : His-tagged human ACTN1 recombinant protein
Lane 4 : His-tagged human ACTN3 recombinant protein
Anti-His tag antibody (1 : 10000) as total protein control.
This antibody does not cross-react with human ACTN1, human ACTN3 and human ACTN4.
All lanes:
Dot Blot - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] (<a href='/en-us/products/primary-antibodies/sarcomeric-alpha-actinin-antibody-epr28776-83-ab317695'>ab317695</a>) at 1/1000 dilution
Lane 1:
His-tagged human ACTN2 recombinant protein
Lane 2:
His-tagged human ACTN4 recombinant protein
Lane 3:
His-tagged human ACTN1 recombinant protein
Lane 4:
His-tagged human ACTN3 recombinant protein
Secondary
All lanes:
Dot Blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Negative control : liver (PMID : 11440986).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] (<a href='/en-us/products/primary-antibodies/sarcomeric-alpha-actinin-antibody-epr28776-83-ab317695'>ab317695</a>) at 1/1000 dilution
Lane 1:
Rat skeletal muscle tissue lysate at 50 µg
Lane 2:
Rat heart tissue lysate at 50 µg
Lane 3:
Rat liver tissue lysate at 50 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 103 kDa,36 kDa
false
Exposure time: 26s
- WB
Supplier Data
Western blot - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] - BSA and Azide free (AB317696)
This data was developed using ab317695, the same antibody clone in a different buffer formulation.
Negative control : liver, placenta (PMID : 11440986).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Exposure time : Lanes 1-2 : 180 seconds, Lanes 3-6 : 26 seconds
All lanes:
Western blot - Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83] (<a href='/en-us/products/primary-antibodies/sarcomeric-alpha-actinin-antibody-epr28776-83-ab317695'>ab317695</a>) at 1/1000 dilution
Lane 1:
Untreated C2C12 (mouse myoblast) whole cell lysate at 50 µg
Lane 2:
C2C12 differentiation to muscle for 5 days whole cell lysate at 50 µg
Lane 3:
Mouse skeletal muscle tissue lysate at 50 µg
Lane 4:
Mouse heart tissue lysate at 50 µg
Lane 5:
Mouse liver tissue lysate at 50 µg
Lane 6:
Mouse placenta tissue lysate at 50 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 103 kDa,36 kDa
false
Related conjugates and formulations (1)
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Anti-Sarcomeric Alpha Actinin antibody [EPR28776-83]
Reactivity data
Product details
ab317696 is the carrier-free version of ab317695.
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.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
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
Sarcomeric alpha actinin associates with multiple proteins to form a complex that coordinates muscle function. It not only serves as a structural component but also participates in signaling processes influencing muscle repair and growth. Alpha actinin connects to other cytoskeletal proteins and adaptors coordinating with integrin pathways to transmit external mechanical signals into cellular responses. The ability of alpha actinin to interact with a range of proteins like filamin and spectrin enhances its role in maintaining cellular architecture.
Pathways
Alpha actinin is critical in both the integrin and dystrophin-glycoprotein complex pathways facilitating signal transduction and maintaining muscle stability. Its interaction with actin filaments is important for pathways involving cell adhesion and motility. Within these pathways actin-related proteins such as ACTN2 and titin partner with alpha actinin to sustain cellular structure and function during dynamic processes including muscle contraction and relaxation.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
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