Anti-SERCA2 ATPase antibody [EPR9393] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal SERCA2 ATPase antibody. Carrier free. Suitable for IHC-P, WB, ICC/IF, Flow Cyt (Intra) and reacts with Mouse, Rat, Human samples. Cited in 1 publication.
View Alternative Names
ATP2B, ATP2A2, Sarcoplasmic/endoplasmic reticulum calcium ATPase 2, SERCA2, SR Ca(2+)-ATPase 2, Calcium pump 2, Endoplasmic reticulum class 1/2 Ca(2+) ATPase
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-SERCA2 ATPase antibody [EPR9393] - BSA and Azide free (AB240095)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab137020).
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HepG2 (human hepatocellular carcinoma epithelial cell) cells labelling SERCA2 ATPase with ab137020 at 1/50 dilution followed by a secondary antibody ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed used at 1/1000 (2 ug/ml) dilution (Green).
Confocal image showing cytoplasmic staining in HepG2 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).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-SERCA2 ATPase antibody [EPR9393] - BSA and Azide free (AB240095)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab137020).
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HeLa (Human cervix adenocarcinoma epithelial cell) cells labelling SERCA2 ATPase with ab137020 at 1/200 dilution (0.25μg) following Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) used at 1/2000 dilution (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).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SERCA2 ATPase antibody [EPR9393] - BSA and Azide free (AB240095)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab137020).
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling SERCA2 ATPase with ab137020 at 1/5000 (0.018 ug/ml) dilution followed by a ready to use LeciaDS9800 (BondTM Polymer Refine Detection). Counterstained with Hematoxylin.
Positive staining on mouse cerebrum.
The section was incubated with ab137020 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0 Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SERCA2 ATPase antibody [EPR9393] - BSA and Azide free (AB240095)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab137020).
Immunohistochemical analysis of paraffin-embedded Mouse lung cancer tissue labeling SERCA2 ATPase with ab137020 at 1/5000 (0.018 ug/ml) dilution followed by a ready to use LeciaDS9800 (BondTM Polymer Refine Detection). Counterstained with Hematoxylin.
Positive staining on mouse lung cancer.
The section was incubated with ab137020 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0 Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SERCA2 ATPase antibody [EPR9393] - BSA and Azide free (AB240095)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab137020).
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling SERCA2 ATPase with ab137020 at 1/5000 (0.018 ug/ml) dilution followed by a ready to use LeciaDS9800 (BondTM Polymer Refine Detection). Counterstained with Hematoxylin.
Positive staining on rat cerebrum.
The section was incubated with ab137020 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0 Epitope Retrieval Solution2) for 20 mins.
- WB
Lab
Western blot - Anti-SERCA2 ATPase antibody [EPR9393] - BSA and Azide free (AB240095)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab137020). We recommend not Boiling the samples after lysis as boiling may cause membrane protein aggregates. ab181602 was used as a GAPDH loading control.
All lanes:
Western blot - Anti-SERCA2 ATPase antibody [EPR9393] (<a href='/en-us/products/primary-antibodies/serca2-atpase-antibody-epr9393-ab137020'>ab137020</a>)
Lane 1:
Jurkat (Human T cell leukemia T lymphocyte) whole cell lysate, boiled at 20 µg
Lane 2:
Jurkat (Human T cell leukemia T lymphocyte) whole cell lysate, unboiled at 20 µg
Lane 3:
C6 (Rat glial tumor glial cell) whole cell lysate, boiled at 20 µg
Lane 4:
C6 (Rat glial tumor glial cell) whole cell lysate, unboiled at 20 µg
Lane 5:
NIH/3T3 (Mouse embryonic fibroblast) whole cell lysate, boiled at 20 µg
Lane 6:
NIH/3T3 (Mouse embryonic fibroblast) whole cell lysate, unboiled at 20 µg
Secondary
All lanes:
Western 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 1/20000 dilution
Observed band size: 115 kDa
false
Exposure time: 20s
Related conjugates and formulations (9)
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Anti-SERCA2 ATPase antibody [EPR9393]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-SERCA2 ATPase antibody [EPR9393]
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578 PE
PE Anti-SERCA2 ATPase antibody [EPR9393]
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660 APC
APC Anti-SERCA2 ATPase antibody [EPR9393]
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HRP Anti-SERCA2 ATPase antibody [EPR9393]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-SERCA2 ATPase antibody [EPR9393]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-SERCA2 ATPase antibody [EPR9393]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-SERCA2 ATPase antibody [EPR9393]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-SERCA2 ATPase antibody [EPR9393]
Reactivity data
Product details
ab240095 is the carrier-free version of ab137020.
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
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The proper regulation of calcium ion levels by SERCA2 ATPase is essential for muscle contraction and relaxation cycles. SERCA2 exists as a part of the complex machinery in muscle cells closely interacting with phospholamban in the cardiac muscle to regulate its activity. Efficient functioning of SERCA2 directly influences calcium ion storage in the sarcoplasmic reticulum affecting muscle physiology and performance.
Pathways
The involvement of SERCA2 ATPase in the calcium signaling pathway and excitation-contraction coupling is significant. The protein's function is intimately linked with RYR2 (ryanodine receptor 2) as they both participate in the regulation of calcium ion flow in muscle cells. This interaction is necessary for the proper release and uptake of calcium ions during muscle contraction and relaxation cycles.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Oncology reports 46: PubMed34528699
2021
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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