Anti-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal Mannose Receptor antibody. Carrier free. Suitable for WB, IHC-P, IHC-Fr, ICC/IF and reacts with Mouse, Rat samples. Cited in 1 publication.
View Alternative Names
CD206, Macrophage mannose receptor 1, MMR, Mrc1
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, 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 Mannose Receptor with ab300621 at 1/50 (9.96 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2ug/mL dilution (Green). Confocal image showing increased cytoplasmic staining in Raw 264.7 cells treated with IL-4 (40ng/ml) for 4 days, then IL-10 (40ng/ml) for another 4 days.Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2ug/mL dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling Mannose Receptor with ab300621 at 1/2000 (0.249 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Positive staining on macrophages and sinusoidal endothelial cells in rat liver (PMID : 25250030). The section was incubated with ab300621 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 a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. 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-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling Mannose Receptor with ab300621 at 1/2000 (0.249 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Positive staining on macrophages and sinusoidal endothelial cells in mouse liver (PMID : 25250030). The section was incubated with ab300621 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 a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat spleen (fresh) tissue labeling Mannose Receptor with ab300621 at 1/500 (0.996 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Positive staining in the red pulp of rat spleen is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution. .
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse lung cancer tissue labeling Mannose Receptor with ab300621 at 1/2000 (0.249 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Positive staining on stroma cells of mouse lung cancer. The section was incubated with ab300621 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 a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. 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-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling Mannose Receptor with ab300621 at 1/2000 (0.249 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Positive staining on mouse spleen (PMID : 28679964). The section was incubated with ab300621 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 a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse spleen (fresh) tissue labeling Mannose Receptor with ab300621 at 1/500 (0.996 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Positive staining in the red pulp of mouse spleen is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution. .
- WB
Lab
Western blot - Anti-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. ab181602 was used as a GAPDH loading control. Samples are non-boiled as boiling may cause protein aggregates. Normal whole brain lysate contains undetectable level of Mannose Receptor in western blot testing, which was also validated by ab125028. PMID : 11320646 reported Mannose Receptor expression in brain is at its highest in the first week of life and dramatically decreases thereafter, being maintained at a low level throughout adulthood.
All lanes:
Western blot - Anti-Mannose Receptor antibody [EPR25215-277] (<a href='/en-us/products/primary-antibodies/mannose-receptor-antibody-epr25215-277-ab300621'>ab300621</a>) at 1/1000 dilution
Lane 1:
Mouse lung tissue lysate at 20 µg
Lane 2:
Mouse liver tissue lysate at 20 µg
Lane 3:
Mouse brain tissue lysate at 20 µg
Lane 4:
Raw264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg
Lane 5:
Raw264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) treated with 20ng/ml IL-4 and 10uM Dexamethasone for 18 hours whole cell lysate at 20 µg
Lane 6:
Rat lung tissue lysate at 20 µg
Lane 7:
Rat liver tissue lysate at 20 µg
Lane 8:
Rat brain tissue 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 1/20000 dilution
Predicted band size: 166 kDa
Observed band size: 200 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-Mannose Receptor antibody [EPR25215-277] - BSA and Azide free (AB300622)
This data was developed using ab300621, the same antibody clone in a different buffer formulation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/1000000 dilution.
All lanes:
Western blot - Anti-Mannose Receptor antibody [EPR25215-277] (<a href='/en-us/products/primary-antibodies/mannose-receptor-antibody-epr25215-277-ab300621'>ab300621</a>) at 1/1000 dilution
Lane 1:
Mouse liver tissue lysate at 10 µg
Lane 2:
Mouse lung tissue lysate at 10 µg
Lane 3:
Mouse spleen tissue at 10 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 1/20000 dilution
Observed band size: 165 kDa
false
Exposure time: 120s
Related conjugates and formulations (8)
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Anti-Mannose Receptor antibody [EPR25215-277]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-Mannose Receptor antibody [EPR25215-277]
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578 PE
PE Anti-Mannose Receptor antibody [EPR25215-277]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-Mannose Receptor antibody [EPR25215-277]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-Mannose Receptor antibody [EPR25215-277]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-Mannose Receptor antibody [EPR25215-277]
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660 APC
APC Anti-Mannose Receptor antibody [EPR25215-277]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-Mannose Receptor antibody [EPR25215-277]
Reactivity data
Product details
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
The Mannose Receptor functions in pathogen recognition and clearance by binding to specific carbohydrates on the pathogen's surface. It is not part of a larger molecular complex but works independently to facilitate phagocytosis. The receptor is essential in immune responses allowing macrophages and dendritic cells to efficiently capture and process antigens for presentation to T cells. This enables the initiation of adaptive immune responses.
Pathways
Researchers know that the Mannose Receptor plays an important role in immune signaling pathways particularly in antigen processing and presentation. It interacts with proteins involved in these pathways including those necessary for the internalization and degradation of bound antigens. Moreover it works alongside scavenger receptors contributing to the regulation of immune and inflammatory responses.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 16:1928 PubMed39994203
2025
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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