Brilliant Violet 510™ anti-mouse/human CD45R/B220 Antibody

2024-07-20

品名: Brilliant Violet 510™ anti-mouse/human CD45R/B220 Antibody

型号: 103248 产品详情 金山科研平台现货促销

Product Details

Isotype Control

Brilliant Violet 510™ Rat IgG2a, κ Isotype Ctrl

Verified Reactivity

Mouse, Human

Reported Reactivity

Cat

Antibody Type

Monoclonal

Host Species

Rat

Immunogen

Abelson murine leukemia virus-induced pre-B tumor cells

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 510™ under optimal conditions.

Concentration

µg size: 0.2 mg/mLµL size: lot-specific (to obtain lot-specific concentration, please enter the lot number in our Concentration and Expiration Lookup or Certificate of Analysis online tools.)

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, IHC-F - 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 using the µl size, 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 flow cytometric staining using the µg size, the suggested use of this reagent is ≤0.5 µg per million cells in 100 µl volume. It is recommended that the reagent be titrated for optimal performance for each application. It is recommended that the reagent be titrated for optimal performance for each application.Brilliant Violet 510™ excites at 405 nm and emits at 510 nm. The bandpass filter 510/50 nm is recommended for detection, although filter optimization may be required depending on other fluorophores used. Be sure to verify that your cytometer configuration and software setup are appropriate for detecting this channel. Refer to your instrument manual or manufacturer for support. Brilliant Violet 510™ 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 RA3-6B2 has been described to react with an epitope on the extracellular domain of the transmembrane CD45 glycoprotein which is dependent upon the expression of exon A and specific carbohydrate residues. Additional reported applications (for the relevant formats) include: immunoprecipitation1, in vitro and in vivo modulation of B cell responses2-4, immunohistochemistry of acetone-fixed frozen sections and formalin-fixed paraffin-embedded sections5,6, and spatial biology (IBEX)14,15.

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)

See More

    Coffman RL. 1982. Immunol. Rev. 69:5. (IP)

    George A, et al. 1994. J. Immunol. 152:1014. (Activ)

    Asensi V, et al. 1989. Immunology 68:204. (Activ)

    Domiati-Saad R, et al. 1993. J. Immunol. 151:5936. (Activ)

    Hata H, et al. 2004. J. Clin. Invest. 114:582. (IHC)

    Monteith CE, et al. 1996. Can. J. Vet. Res. 60:193. (IHC)

    Shih FF, et al. 2006. J. Immunol. 176:3438. (FC)

    Chang C L-T, et al. 2007. J. Immunol. 178:6984.

    Fazilleau N, et al. 2007. Nature Immunol. 8:753.

    Lang GL, et al. 2008. Blood 111:2158. PubMed

    Charles N, et al. 2010. Nat. Med. 16:701. (FC) PubMed

    del Rio ML, et al. 2011. Transpl. Int. 24:501. (FC) PubMed

Product Citations

See More

    Huang L, et al. 2017. PLoS Biol.. 10.1371/journal.pbio.2001750. PubMed

    Reismann D, et al. 2017. Nat Commun.. 10.1038/s41467-017-01538-9. PubMed

    Webster P, et al. 2018. Nat Commun. 9:2649. PubMed

    Dietmar Herndler‐Brandstetter et al. 2018. Immunity. 48(4):716-729 . PubMed

    Orr MT, et al. 2019. NPJ Vaccines. 4:1. PubMed

    Abdel Malik R, et al. 2017. Circ Res. 120:99. PubMed

    Barbet G, et al. 2018. Immunity. 48:584. PubMed

    Yen WF et al. 2019. Cell reports. 27(5):1472-1486 . PubMed

    Schoeler K, et al. 2019. FEBS J. 10.1111/febs.14934. PubMed

    Barry KC, et al. 2018. Nat Med. 24:1178. PubMed

    Franks SE, et al. 2019. J Immunol. 202:3381. PubMed

    Matundan H, et al. 2019. J Virol. 93. PubMed

RRID

AB_2561394 (BioLegend Cat. No. 103247) AB_2650679 (BioLegend Cat. No. 103248)

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