- Clone
- C068C2 (See other available formats)
- Regulatory Status
- RUO
- Other Names
- MMR (macrophage mannose receptor), MR (mannose receptor), MRC1
- Isotype
- Rat IgG2a, κ
- Ave. Rating
- Submit a Review
- Product Citations
- publications
Cat # | Size | Price | Quantity Check Availability | Save | ||
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141717 | 125 µL | £140 |
CD206, also known as mannose receptor (MR), is a 175 kD type I membrane protein. It is a pattern recognition receptor (PRR) belonging to the C-type lectin superfamily. MR is expressed on macrophages, dendritic cells, Langerhans cells, and hepatic or lymphatic endothelial cells. MR recognizes a range of microbial carbohydrates bearing mannose, fucose, or N-acetyl glucosamine through its C-type lectin-like carbohydrate recognition domains, sulfated carbohydrate antigens through its cysteine-rich domain, and collagens through its fibronectin type II domain. MR mediates endocytosis and phagocytosis as well as activation of macrophages and antigen presentation. It plays an important role in host defense and provides a link between innate and adaptive immunity. Recently, MR on lymphatic endothelial cells was found to be involved in leukocyte trafficking and a contributor to the metastatic behavior of cancer cells. It suggests that MR may be a potential target in controlling inflammation and cancer metastasis by targeting the lymphatic vasculature.
Product DetailsProduct Details
- Verified Reactivity
- Mouse
- Antibody Type
- Monoclonal
- Host Species
- Rat
- Immunogen
- Recombinant mouse CD206 (MMR)
- Formulation
- Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and BSA (origin USA).
- Preparation
- The antibody was purified by affinity chromatography and conjugated with Brilliant Violet 421™ under optimal conditions.
- Concentration
- Lot-specific (to obtain lot-specific concentration and expiration, please enter the lot number in our Certificate of Analysis online tool.)
- Storage & Handling
- The antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
- Application
-
ICFC - Quality tested
FC, IHC-F - VerifiedSB - Reported in the literature, not verified in house
- Recommended Usage
-
Each lot of this antibody is quality control tested by intracellular immunofluorescent staining with flow cytometric analysis. For flow cytometric staining, the suggested use of this reagent is 5 µL per million cells in 100 µL staining volume or 5 µL per 100 µL of whole blood. For immunohistochemistry on frozen tissue sections, a concentration range of 2.5 - 5.0 µg/mL is suggested. It is recommended that the reagent be titrated for optimal performance for each application.
Brilliant Violet 421™ excites at 405 nm and emits at 421 nm. The standard bandpass filter 450/50 nm is recommended for detection. Brilliant Violet 421™ is a trademark of Sirigen Group Ltd.
Learn more about Brilliant Violet™.
This product is subject to proprietary rights of Sirigen Inc. and is made and sold under license from Sirigen Inc. The purchase of this product conveys to the buyer a non-transferable right to use the purchased product for research purposes only. This product may not be resold or incorporated in any manner into another product for resale. Any use for therapeutics or diagnostics is strictly prohibited. This product is covered by U.S. Patent(s), pending patent applications and foreign equivalents. - Excitation Laser
-
Violet Laser (405 nm)
- Application Notes
-
Clone C068C2 recognizes a region similar to clone MR5D3, based on the ability of the clones to block each other. Additional reported applications (for the relevant formats) include: spatial biology (IBEX)4,5.
- Additional Product Notes
-
Iterative Bleaching Extended multi-pleXity (IBEX) is a fluorescent imaging technique capable of highly-multiplexed spatial analysis. The method relies on cyclical bleaching of panels of fluorescent antibodies in order to image and analyze many markers over multiple cycles of staining, imaging, and, bleaching. It is a community-developed open-access method developed by the Center for Advanced Tissue Imaging (CAT-I) in the National Institute of Allergy and Infectious Diseases (NIAID, NIH).
-
Application References
(PubMed link indicates BioLegend citation) -
- Keller J, et al. 2012. Biochem Biophys Res Commun. 417:217. PubMed
- Ito H, et al. 2012. J Am Soc Nephrol. 23:1797. PubMed
- Yang X, et al. 2015. PNAS. 112:2900. PubMed
- Radtke AJ, et al. 2020. Proc Natl Acad Sci U S A. 117:33455-65. (SB) PubMed
- Radtke AJ, et al. 2022. Nat Protoc. 17:378-401. (SB) PubMed
- Product Citations
-
- RRID
-
AB_2562232 (BioLegend Cat. No. 141717)
Antigen Details
- Structure
- Type I transmembrane protein, 175 kD, C-type lectin superfamily
- Distribution
-
Macrophages, dendritic cells, Langerhans cells, liver endothelial cells
- Function
- Pathogen recognition, endocytosis and phagocytosis, antigen presentation
- Ligand/Receptor
- Antigen containing mannose, fucose, or an N-acetyl glucosamine
- Cell Type
- Dendritic cells, Endothelial cells, Langerhans cells, Macrophages
- Biology Area
- Cell Biology, Immunology, Innate Immunity, Signal Transduction
- Molecular Family
- CD Molecules
- Antigen References
-
1. Wileman TE, et al. 1986. P. Natl. Acad. Sci. USA 83:2501.
2. Apostolopoulos V, et al. 2001. Curr. Mol. Med. 1:469.
3. Burgdorf S, et al. 2006. J. Immunol. 176:6770.
4. McKenzie EJ, et al. 2007. J. Immunol. 178:4975. - Gene ID
- 17533 View all products for this Gene ID
- UniProt
- View information about CD206 on UniProt.org
Related Pages & Pathways
Pages
Related FAQs
- Why is mouse CD206 stained intracellularly and not via surface staining?
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Typically, mouse CD206 surface level is relatively low under normal conditions and so intracellular staining protocol is required to get better signal.
- What is the F/P ratio range of our BV421™ format antibody reagents?
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It is lot-specific. On average it ranges between 2-4.
- If an antibody clone has been previously successfully used in IBEX in one fluorescent format, will other antibody formats work as well?
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It’s likely that other fluorophore conjugates to the same antibody clone will also be compatible with IBEX using the same sample fixation procedure. Ultimately a directly conjugated antibody’s utility in fluorescent imaging and IBEX may be specific to the sample and microscope being used in the experiment. Some antibody clone conjugates may perform better than others due to performance differences in non-specific binding, fluorophore brightness, and other biochemical properties unique to that conjugate.
- Will antibodies my lab is already using for fluorescent or chromogenic IHC work in IBEX?
-
Fundamentally, IBEX as a technique that works much in the same way as single antibody panels or single marker IF/IHC. If you’re already successfully using an antibody clone on a sample of interest, it is likely that clone will have utility in IBEX. It is expected some optimization and testing of different antibody fluorophore conjugates will be required to find a suitable format; however, legacy microscopy techniques like chromogenic IHC on fixed or frozen tissue is an excellent place to start looking for useful antibodies.
- Are other fluorophores compatible with IBEX?
-
Over 18 fluorescent formats have been screened for use in IBEX, however, it is likely that other fluorophores are able to be rapidly bleached in IBEX. If a fluorophore format is already suitable for your imaging platform it can be tested for compatibility in IBEX.
- The same antibody works in one tissue type but not another. What is happening?
-
Differences in tissue properties may impact both the ability of an antibody to bind its target specifically and impact the ability of a specific fluorophore conjugate to overcome the background fluorescent signal in a given tissue. Secondary stains, as well as testing multiple fluorescent conjugates of the same clone, may help to troubleshoot challenging targets or tissues. Using a reference control tissue may also give confidence in the specificity of your staining.
- How can I be sure the staining I’m seeing in my tissue is real?
-
In general, best practices for validating an antibody in traditional chromogenic or fluorescent IHC are applicable to IBEX. Please reference the Nature Methods review on antibody based multiplexed imaging for resources on validating antibodies for IBEX.
Other Formats
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Compare Data Across All Formats
This data display is provided for general comparisons between formats.
Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
If you need assistance with selecting the best format contact our expert technical support team.
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Biotin anti-mouse CD206 (MMR)
Thioglycollate-elicited Balb/c peritoneal macrophages were s... -
Purified anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c mouse peritoneal macrophages ... -
FITC anti-mouse CD206 (MMR)
Thioglycollate-elicited Balb/c macrophages were fixed/pemeab... -
PE anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c peritoneal macrophages were s... -
APC anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c peritoneal macrophages were s... -
Alexa Fluor® 488 anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c peritoneal macrophages were s... C57BL/6 mouse frozen lymph node section fixed, permeabilized... -
Alexa Fluor® 647 anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c peritoneal macrophages were s... C57BL/6 mouse frozen lymph node section was fixed with 4% pa... -
PerCP/Cyanine5.5 anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c mouse peritoneal macrophages ... -
PE/Cyanine7 anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c mouse peritoneal macrophages ... -
Brilliant Violet 421™ anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c mouse peritoneal macrophages ... C57BL/6 mouse frozen lymph node section was fixed with 4% pa... Confocal image of C57BL/6 mouse thymus sample acquired using... Confocal image of C57BL/6 mouse lung sample acquired using t... Mice were injected subcutaneously with sheep red blood cells... Mice were injected subcutaneously with sheep red blood cells... -
Brilliant Violet 605™ anti-mouse CD206 (MMR)
Thioglycollate-elicited Balb/c peritoneal macrophages were f... -
Brilliant Violet 650™ anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c mouse peritoneal macrophages ... -
Alexa Fluor® 594 anti-mouse CD206 (MMR)
C57BL/6 mouse frozen spleen section was fixed with 4% parafo... -
Brilliant Violet 711™ anti-mouse CD206 (MMR)
Thioglycollate-elicited Balb/c peritoneal macrophages were f... -
Brilliant Violet 785™ anti-mouse CD206 (MMR)
Thioglycollate-elicited Balb/c peritoneal macrophages were f... -
PE/Dazzle™ 594 anti-mouse CD206 (MMR)
Thioglycollate-elicited Balb/c peritoneal macrophages were f... -
Alexa Fluor® 700 anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c peritoneal macrophages were f... -
Spark YG™ 570 anti-mouse CD206 (MMR)
C57BL/6 mouse frozen spleen section was fixed with 4% parafo... -
PE/Cyanine5 anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c peritoneal macrophages were f... -
PE/Fire™ 700 anti-mouse CD206 (MMR)
Thioglycollate-elicited BALB/c peritoneal macrophages were s... -
TotalSeq™-B0173 anti-mouse CD206 (MMR)
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Spark Red™ 718 anti-mouse CD206 (MMR) (Flexi-Fluor™)
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Spark Blue™ 574 anti-mouse CD206 (MMR) (Flexi-Fluor™)
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