Anti-MS4A2 antibody [EPR24324-7] - BSA and Azide free (ab280570)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR24324-7] to MS4A2 - BSA and Azide free
- Suitable for: Dot blot, ICC, IP, IHC-P
- Reacts with: Human
Overview
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Product name
Anti-MS4A2 antibody [EPR24324-7] - BSA and Azide free
See all MS4A2 primary antibodies -
Description
Rabbit monoclonal [EPR24324-7] to MS4A2 - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: Dot blot, ICC, IP, IHC-Pmore details
Unsuitable for: Flow Cyt (Intra) or WB -
Species reactivity
Reacts with: Human -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- IHC-P: Human colon, breast carcinoma and prostatic hyperplasia tissue. ICC: HEK-293T cells. IP: HEK-293T cell. Dot Blot: Human MS4A2 peptide.
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General notes
ab280570 is the carrier-free version of ab271068. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
ab280570 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. -
Storage buffer
Constituent: 100% PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR24324-7 -
Isotype
IgG -
Research areas
Images
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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
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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.
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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.
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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
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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.
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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.
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