Anti-Extracellular matrix protein 1 antibody [EPR22411-279] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal Extracellular matrix protein 1 antibody. Carrier free. Suitable for IP, WB, IHC-P, Flow Cyt (Intra) and reacts with Mouse, Rat samples.
View Alternative Names
Extracellular matrix protein 1, Secretory component p85, Ecm1
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-Extracellular matrix protein 1 antibody [EPR22411-279] - BSA and Azide free (AB267392)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and sodium azide (ab253185).
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90%, methanol permeabilized 4T1 (mouse mammary gland carcinoma epithelial cell) cells labeling Extracellular matrix protein 1 with ab253185 at 1/500 (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
- IP
Unknown
Immunoprecipitation - Anti-Extracellular matrix protein 1 antibody [EPR22411-279] - BSA and Azide free (AB267392)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and sodium azide (ab253185).
Extracellular matrix protein 1 was immunoprecipitated from 0.35 mg mouse liver lysate with ab253185 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab253185 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse liver lysate 10μg.
Lane 2 : ab253185 IP in mouse liver lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab253185 in mouse liver lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 mins.
All lanes:
Immunoprecipitation - Anti-Extracellular matrix protein 1 antibody [EPR22411-279] (<a href='/en-us/products/primary-antibodies/extracellular-matrix-protein-1-antibody-epr22411-279-ab253185'>ab253185</a>)
Predicted band size: 61 kDa
Observed band size: 85 kDa
false
- IP
Unknown
Immunoprecipitation - Anti-Extracellular matrix protein 1 antibody [EPR22411-279] - BSA and Azide free (AB267392)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and sodium azide (ab253185).
Extracellular matrix protein 1 was immunoprecipitated from 0.35 mg mouse lung lysate with ab253185 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab253185 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse lung lysate 10μg.
Lane 2 : ab253185 IP in mouse lung lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab253185 in mouse lung lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 30 seconds.
All lanes:
Immunoprecipitation - Anti-Extracellular matrix protein 1 antibody [EPR22411-279] (<a href='/en-us/products/primary-antibodies/extracellular-matrix-protein-1-antibody-epr22411-279-ab253185'>ab253185</a>)
Predicted band size: 61 kDa
Observed band size: 85 kDa
false
- WB
Unknown
Western blot - Anti-Extracellular matrix protein 1 antibody [EPR22411-279] - BSA and Azide free (AB267392)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and sodium azide (ab253185).
The wild-type and ECM1 knockout mouse liver lysates were kindly provided by an anonymous collaborator.
ab253185 was shown to specifically react with Extracellular matrix protein 1 in wild-type mouse liver as signal was lost in ECM1 knockout liver. Wild-type and ECM1 knockout samples were subjected to SDS-PAGE. ab253185 and ab181602 (Rabbit anti-GAPDH loading control) were incubated 1 hour at room temperature at 1/1000 dilution and 1/200,000 dilution respectively. Blots were developed with Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) secondary antibody at 1/50,000 dilution for 1 hour at room temperature before imaging. The blot was developed on a BIO-RAD® ChemiDoc™ MP instrument using the ECL technique.
Exposure time 7.75 secs.
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Extracellular matrix protein 1 antibody [EPR22411-279] (<a href='/en-us/products/primary-antibodies/extracellular-matrix-protein-1-antibody-epr22411-279-ab253185'>ab253185</a>) at 1/1000 dilution
Lane 1:
Wild-type mouse liver lysate at 20 µg
Lane 2:
ECM1 knockout mouse liver lysate 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 1/100000 dilution
Predicted band size: 61 kDa
Observed band size: 48 kDa,85 kDa
false
Related conjugates and formulations (1)
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Anti-Extracellular matrix protein 1 antibody [EPR22411-279]
Reactivity data
Product details
ab267392 is the carrier-free version of ab253185.
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
ECM1 contributes to cell-matrix interactions and regulates various cell behaviors such as adhesion proliferation and differentiation. It does this by binding to other ECM proteins and is known not to be part of a specific complex. ECM1 facilitates communication between the cellular environment and matrix thereby supporting the architecture and dynamics of tissues. It modulates angiogenesis linking it with processes like wound healing and vascular development.
Pathways
ECM1 functions within the context of key signaling routes such as the PI3K/AKT pathway known for roles in cell growth and survival. ECM1 interacts with other proteins including matrix metalloproteinases contributing to matrix remodeling activities important for cellular migration and invasion. Cumulatively these interactions highlight ECM1’s place in connective tissue organization and regenerative processes.
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