Anti-Arc antibody [EPR18950] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(2 Publications)
Rabbit Recombinant Monoclonal ARC antibody. Carrier free. Suitable for IHC-P, IP, WB and reacts with Mouse, Rat, Human samples. Cited in 2 publications.
View Alternative Names
KIAA0278, ARC, Activity-regulated cytoskeleton-associated protein, hArc, Activity-regulated gene 3.1 protein homolog, ARC/ARG3.1, Arg3.1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Arc antibody [EPR18950] - BSA and Azide free (AB224717)
Immunohistochemical analysis of paraffin-embedded mouse cerebral cortex tissue labeling Arc with ab183183 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) ready to use. Nuclear staining on neurons of mouse cerebral cortex. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) ready to use.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab183183).
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Arc antibody [EPR18950] - BSA and Azide free (AB224717)
Immunohistochemical analysis of paraffin-embedded mouse hippocampus tissue labeling Arc with ab183183 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) ready to use. Sparse nuclear staining (arrows) in the dentate gyrus of mouse hippocampus (PMID : 19750198, PMID : 19628007). Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) ready to use.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab183183).
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IP
Supplier Data
Immunoprecipitation - Anti-Arc antibody [EPR18950] - BSA and Azide free (AB224717)
Arc was immunoprecipitated from 0.35 mg of mouse brain lysate with ab183183 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab183183 at 1/500 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/1000 dilution.
Lane 1 : Mouse brain lysate 10 μg (Input).
Lane 2 : ab183183 IP in mouse brain lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab183183 in mouse brain lysate.
Exposure time : 1 second
Blocking/dilution buffer : 5% NFDM/TBST.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab183183).
All lanes:
Immunoprecipitation - Anti-Arc antibody [EPR18950] (<a href='/en-us/products/primary-antibodies/arc-antibody-epr18950-ab183183'>ab183183</a>)
Predicted band size: 42 kDa,45 kDa,75 kDa
Observed band size: 42 kDa,45 kDa,75 kDa
false
- WB
Lab
Western blot - Anti-Arc antibody [EPR18950] - BSA and Azide free (AB224717)
False colour image of Western blot : Anti-Arc antibody [EPR18950] staining at 1/500 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab183183 was shown to bind specifically to Arc. A band was observed at 45 kDa in wild-type Neuro-2a cell lysates with no signal observed at this size in arc knockout cell line ab280071 (knockout cell lysate ab280130). To generate this image, wild-type and arc knockout Neuro-2a cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in fluorescent western blot (TBS-based) blocking solution before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab183183).
All lanes:
Western blot - Anti-Arc antibody [EPR18950] (<a href='/en-us/products/primary-antibodies/arc-antibody-epr18950-ab183183'>ab183183</a>) at 1/500 dilution
Lane 1:
Wild-type Neuro-2a cell lysate at 20 µg
Lane 2:
ARC knockout Neuro-2a cell lysate at 20 µg
Lane 2:
Western blot - Mouse ARC knockout Neuro-2a cell line (<a href='/en-us/products/cell-lines/mouse-arc-knockout-neuro-2a-cell-line-ab280071'>ab280071</a>)
Lane 3:
SH-SY5Y cell lysate at 20 µg
Lane 4:
K562 cell lysate at 20 µg
Lane 5:
Mouse Brain cell lysate at 20 µg
Predicted band size: 45 kDa
Observed band size: 45 kDa
false
Related conjugates and formulations (1)
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Anti-Arc antibody [EPR18950]
Reactivity data
Product details
ab224717 is the carrier-free version of ab183183.
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
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The Arc protein influences synaptic plasticity and memory formation. It does not operate alone; instead it interacts within complexes that regulate synaptic strength. These complexes contain other proteins critical for actin cytoskeleton remodeling which impacts synaptic efficacy. Through these interactions Arc supports the internalization of AMPA receptors playing a role in long-term depression (LTD) and long-term potentiation (LTP) of synapses essential mechanisms for learning and memory.
Pathways
The Arc protein forms integral parts of the synaptic signaling pathways. It connects with the BDNF-TrkB signaling pathway which is important for neuronal development and synaptic modulation. Arc also relates to the mTOR signaling pathway which governs cellular growth and protein synthesis. Through these pathways Arc interacts with proteins like Neuro2a and SynGAP highlighting its comprehensive role in synaptic regulation and plasticity.
Product protocols
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Target data
Publications (2)
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Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 39:1624-1641 PubMed38402460
2024
Applications
Unspecified application
Species
Unspecified reactive species
Journal of pain research 13:345-354 PubMed32104056
2020
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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