Anti-MS4A2 antibody [EPR24324-7] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal MS4A2 antibody. Carrier free. Suitable for ICC/IF, IP, Dot, IHC-P and reacts with Human, Recombinant fragment - Human, Synthetic peptide - Human samples.
View Alternative Names
APY, FCER1B, IGER, MS4A2, High affinity immunoglobulin epsilon receptor subunit beta, FcERI, Fc epsilon receptor I beta-chain, IgE Fc receptor subunit beta, Membrane-spanning 4-domains subfamily A member 2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MS4A2 antibody [EPR24324-7] - BSA and Azide free (AB280570)
This data was developed using ab271068, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue labelling MS4A2 with ab271068 at 1/2000 dilution (0.221 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Membranous staining on mast cells of human breast carcinoma. The section was incubated with ab271068 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 ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-MS4A2 antibody [EPR24324-7] - BSA and Azide free (AB280570)
This data was developed using ab271068, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HEK-293T cells labelling MS4A2 with ab271068 at 1/500 dilution, followed by ab150080 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) antibody at 1/500 dilution (Red).
Confocal image showing cytoplasmic staining in HEK-293T cells transfected with myc-tagged MS4A2 expression vector (PMID : 18571665).
ab202008 Anti-Myc tag mouse monoclonal antibody (Alexa Fluor® 488) was used to counterstain tubulin at 1/100 dilution (Green). The nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150080 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) at 1/500 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MS4A2 antibody [EPR24324-7] - BSA and Azide free (AB280570)
This data was developed using ab271068, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human prostatic hyperplasia tissue labelling MS4A2 with ab271068 at 1/2000 dilution (0.221 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Membranous staining on mast cells of human prostatic hyperplasia. The section was incubated with ab271068 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 ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval 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-MS4A2 antibody [EPR24324-7] - BSA and Azide free (AB280570)
This data was developed using ab271068, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human colon tissue labelling MS4A2 with ab271068 at 1/2000 dilution (0.221 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Membranous staining on mast cells of human colon. The section was incubated with ab271068 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 ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IP
Supplier Data
Immunoprecipitation - Anti-MS4A2 antibody [EPR24324-7] - BSA and Azide free (AB280570)
This data was developed using ab271068, the same antibody clone in a different buffer formulation.
MS4A2 was immunoprecipitated from 0.35 mg HEK-293T (human embryonic kidney) transfected with MS4A2 expression vector, whole cell lysate 10 μg with ab271068 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab271068 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : HEK-293T transfected with MS4A2 expression vector, whole cell lysate 10 μg
Lane 2 : ab271068 IP in HEK-293T transfected with MS4A2 expression vector, whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab271068 in HEK-293T transfected with MS4A2 expression vector, whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 7.75 seconds
All lanes:
Immunoprecipitation - Anti-MS4A2 antibody [EPR24324-7] (<a href='/en-us/products/primary-antibodies/ms4a2-antibody-epr24324-7-ab271068'>ab271068</a>)
Predicted band size: 27 kDa
false
- Dot
Supplier Data
Dot Blot - Anti-MS4A2 antibody [EPR24324-7] - BSA and Azide free (AB280570)
This data was developed using ab271068, the same antibody clone in a different buffer formulation.
Dot blot analysis of MS4A2 using ab271068 at 1 : 1000 dilution followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Lane 1 : Human MS4A2 peptide (aa 226-243)
Lane 2 : Human MS4A2 peptide (aa 206-223)
Lane 3 : Human MS4A2 peptide (aa 151-171)
Exposure time : 3 minutes
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Related conjugates and formulations (1)
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Anti-MS4A2 antibody [EPR24324-7]
Reactivity data
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
MS4A2 contributes significantly to the immune system by participating in allergic response signaling. It assembles with other subunits — alpha and gamma — to form the tetrameric IgE receptor complex. This complex on mast cells and basophils detects IgE antibodies bound to allergens triggering the release of inflammatory mediators like histamine. These mediators lead to symptoms associated with allergic reactions such as asthma and anaphylaxis. MS4A2's interaction with allergens through the receptor complex makes it an essential player in immune surveillance and response.
Pathways
MS4A2 directly influences the Fc epsilon RI signaling pathway an essential component in immune responses especially related to allergy and hypersensitivity reactions. The pathway not only involves MS4A2 but also proteins like Lyn and Syk kinase which further relay the signals initiated by antigen-IgE binding. This interaction can lead to robust downstream immune responses including inflammatory processes. The MS4A2 protein's role in this pathway connects it with other signaling cascades enhancing cell activation and response.
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