Pacific Blue™ anti-mouse CD21/CD35 (CR2/CR1) Antibody

Product Details

Verified Reactivity

Mouse

Antibody Type

Monoclonal

Host Species

Rat

Immunogen

CD35/CFA

Formulation

Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.

Preparation

The antibody was purified by affinity chromatography, and conjugated with Pacific Blue™ under optimal conditions.

Concentration

0.5 mg/ml

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

FC - Quality tested

SB - Reported in the literature, not verified in house

Recommended Usage

Each lot of this antibody is quality control tested by immunofluorescent staining with flow cytometric analysis. For flow cytometric staining, the suggested use of this reagent is ≤ 1.0 µg per 10⁶ cells in 100 µl volume. It is recommended that the reagent be titrated for optimal performance for each application.

* Pacific Blue™ has a maximum emission of 455 nm when it is excited at 405 nm. Prior to using Pacific Blue™ conjugate for flow cytometric analysis, please verify your flow cytometer's capability of exciting and detecting the fluorochrome.

Alexa Fluor® and Pacific Blue™ are trademarks of Life Technologies Corporation.

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Excitation Laser

Violet Laser (405 nm)

Application Notes

Additional reported application (for relevant formats) include: spatial biology (IBEX)^5,6.

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

1. Boackle S, et al. 2001 Immunity 15:775.
2. de Andres B, et al. 2012. J. Immunol. 189:2300. PubMed
3. Chiu YK, et al. 2014. J Immunol. 193:2207. PubMed
4. Koening PA, et al. 2014. J Biol Chem. 289:34490. PubMed
5. Radtke AJ, et al. 2020. Proc Natl Acad Sci U S A. 117:33455-65. (SB) PubMed
6. Radtke AJ, et al. 2022. Nat Protoc. 17:378-401. (SB) PubMed

Product Citations

1. Voss LF, et al. 2023. Front Immunol. 13:1021370. PubMed
2. Lütge M, et al. 2023. Nat Immunol. . PubMed
3. Bhattacharya Y 2014. J Exp Med. 211:841. PubMed
4. Farsakoglu Y et al. 2019. Cell reports. 26(9):2307-2315 . PubMed
5. Menzel L, et al. 2021. Cell Rep. 37:109878. PubMed
6. Juul-Madsen K, et al. 2021. Proc Natl Acad Sci U S A. 118:. PubMed
7. Dubey LK, et al. 2019. Cell Rep. 27:2442. PubMed
8. Avery DT, et al. 2018. J Exp Med. 215:2073. PubMed
9. Duan L, et al. 2021. Immunity. 54:2256. PubMed
10. Onodera T, et al. 2016. J Immunol. 196: 4172 - 4184. PubMed
11. Duong B, et al. 2010. J Exp Med. 207:173. PubMed
12. Noviski M, et al. 2018. Elife. 7:e35074. PubMed
13. Lofano G, et al. 2015. J Immunol. 195: 1617-1627. PubMed
14. Simoni L, et al. 2020. Cell Rep. 33:108330. PubMed
15. Seeley-Fallen M, et al. 2014. Proc Natl Acad Sci U S A. 111:9881. PubMed
16. Radice E, et al. 2020. Cell Reports. 32(5):107951. PubMed
17. Gill R, et al. 2017. Toxicol Appl Pharmacol. 330:22. PubMed

RRID

AB_2085158 (BioLegend Cat. No. 123413)
AB_2085158 (BioLegend Cat. No. 123414)

Antigen Details

Structure

145 kD/190 kD type I transmembrane glycoprotein

Distribution

B cells, follicular dendritic cells

Function

Signal transduction

Ligand/Receptor

Associated with CD19/CD81. CD21 binds C3d, iC3b, and EBV; CD35 binds C3b, iC3b, C4b, and iC4b.

Cell Type

B cells, Dendritic cells

Biology Area

Cell Biology, Costimulatory Molecules, Immunology, Neuroinflammation, Neuroscience

Molecular Family

Adhesion Molecules, CD Molecules

Antigen References

1. Kozono Y, et al. 1998. J. Immunol. 160:1562.
2. Shimizu I, et al. 2007. Blood 109:1773.
3. Roozendaal R and MC. Carroll. 2007. Immunol. Rev. 219:157.

Gene ID

12902 View all products for this Gene ID 12946 View all products for this Gene ID

UniProt

View information about CD21/CD35 on UniProt.org

Documentation

• Technical Data Sheet (pdf)
• Certificate of Analysis
• Material Safety Data Sheet

Reviews

Related Protocols

• Cell Surface Flow Cytometry Staining Protocol

Related Pages & Pathways

Related FAQs

If an antibody clone has been previously successfully used in IBEX in one fluorescent format, will other antibody formats work as well?

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

Certificate of Analysis