重组Anti-SAA3抗体[EPR23102-242] - BSA and Azide free
Anti-SAA3 antibody [EPR23102-242] - BSA and Azide free
- RabMAb
- Recombinant
- 了解详情
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Rabbit Recombinant Monoclonal SAA3 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra) and reacts with Mouse, Rat, Recombinant fragment - Mouse samples.
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Serum amyloid A-3 protein, Saa3
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SAA3 antibody [EPR23102-242] - BSA and Azide free (AB280893)
This data was developed using ab233547, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cells labelling SAA3 with ab233547 at 1/50 dilution (9.18 ug/ml), followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing cytoplasmic staining in RAW 264.7 cells is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-SAA3 antibody [EPR23102-242] - BSA and Azide free (AB280893)
This data was developed using ab233547, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cells labelling SAA3 with ab233547 at 1/500 dilution (0.1ug) (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). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
- IP
Supplier Data
Immunoprecipitation - Anti-SAA3 antibody [EPR23102-242] - BSA and Azide free (AB280893)
This data was developed using ab233547, the same antibody clone in a different buffer formulation.
SAA3 was immunoprecipitated from 0.35 mg of Mouse colon tissue lysate with ab233547 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab233547 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse colon tissue lysate 10 ug
Lane 2 : ab233547 IP in Mouse colon tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab233547 in Mouse colon tissue lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 15 seconds
All lanes:
Immunoprecipitation - Anti-SAA3 antibody [EPR23102-242] (<a href='/products/primary-antibodies/saa3-antibody-epr23102-242-ab233547'>ab233547</a>)
false
- WB
Lab
Western blot - Anti-SAA3 antibody [EPR23102-242] - BSA and Azide free (AB280893)
This data was developed using ab233547, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Low expression : kidney and heart (PMID : 29056547)
Exposure time : 92 seconds
All lanes:
Western blot - Anti-SAA3 antibody [EPR23102-242] (<a href='/products/primary-antibodies/saa3-antibody-epr23102-242-ab233547'>ab233547</a>) at 1/1000 dilution
Lane 1:
Rat colon tissue lysate at 20 µg
Lane 2:
Rat liver tissue lysate at 20 µg
Lane 3:
Rat spleen tissue lysate at 20 µg
Lane 4:
Rat kidney tissue lysate at 20 µg
Lane 5:
Rat heart tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 14 kDa
false
- WB
Lab
Western blot - Anti-SAA3 antibody [EPR23102-242] - BSA and Azide free (AB280893)
This data was developed using ab233547, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Low expression : kidney and heart (PMID : 29056547)
Exposure time : 92 seconds
All lanes:
Western blot - Anti-SAA3 antibody [EPR23102-242] (<a href='/products/primary-antibodies/saa3-antibody-epr23102-242-ab233547'>ab233547</a>) at 1/1000 dilution
Lane 1:
Mouse colon tissue lysate at 20 µg
Lane 2:
Mouse liver tissue lysate at 20 µg
Lane 3:
Mouse kidney tissue lysate at 20 µg
Lane 4:
Mouse heart tissue lysate at 20 µg
Lane 5:
RAW 264.7 (mouse abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg
Lane 6:
J774A.1 (mouse reticulum cell sarcoma monocyte macrophage) whole cell lysate at 20 µg
Lane 7:
NR8383 (rat norvegicus lung macrophage (alveolar)) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 14 kDa
false
- WB
Lab
Western blot - Anti-SAA3 antibody [EPR23102-242] - BSA and Azide free (AB280893)
This data was developed using ab233547, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time : 26 seconds
All lanes:
Western blot - Anti-SAA3 antibody [EPR23102-242] (<a href='/products/primary-antibodies/saa3-antibody-epr23102-242-ab233547'>ab233547</a>) at 1/1000 dilution
Lane 1:
His-tagged mouse Saa1 recombinant protein (aa 20-122) at 0.02 µg
Lane 2:
E.coli extracts containing his-tagged mouse Saa2 recombinant protein (aa 20-122) at 20 µL
Lane 3:
His/lif-tagged mouse Saa3 recombinant protein (aa 19-122) at 0.01 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
false
不同偶联物与剂型 (3)
-
Anti-SAA3 antibody [EPR23102-242]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-SAA3 antibody [EPR23102-242]
-
578 PE
PE Anti-SAA3 antibody [EPR23102-242]
反应性数据
产品详情
ab280893 is the carrier-free version of ab233547.
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.
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存条件
推荐的长期储存条件
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
SAA3 modulates inflammatory responses and may play a role in the pathogenesis of chronic inflammatory diseases. SAA3 proteins can associate with high-density lipoprotein (HDL) in the bloodstream. Such association changes the lipid metabolism and cholesterol transport affecting the body's inflammatory state. The protein also participates in attracting immune cells like leukocytes to the site of inflammation contributing to immune surveillance and tissue repair.
Pathways
Several studies show that SAA3 participates in the toll-like receptor (TLR) signaling and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB) pathways. These pathways are key regulators of the immune response. SAA3 activation can lead to increased cytokine production such as interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-alpha). Its interactions with other SAAs suggest an overlap in their immune-modulating roles making them important players in systemic inflammation.
产品实验方案
- Visit the General protocols
- Visit the Troubleshooting
靶点信息
Abcam 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