ArC™ Amine Reactive Compensation Bead Kit (for use with LIVE/DEAD™ Fixable dead cell stain kits)
ArC™ Amine Reactive Compensation Bead Kit (for use with LIVE/DEAD™ Fixable dead cell stain kits)
Invitrogen™

ArC™ Amine Reactive Compensation Bead Kit (for use with LIVE/DEAD™ Fixable dead cell stain kits)

ArC™ Amine Reactive Compensation Bead Kit is a bead-based compensation tool specifically optimized for use with LIVE/DEAD™ Fixable dead cellRead more
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Catalog NumberNo. of Tests
A10346100
A1062825
Catalog number A10346
Price (TWD)
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No. of Tests:
100
Price (TWD)
***
Add to cart
ArC™ Amine Reactive Compensation Bead Kit is a bead-based compensation tool specifically optimized for use with LIVE/DEAD™ Fixable dead cell stain kits.

• Ready-to-use control
• Eliminates the hassle of heat-treating cells as a control, saving precious sample
• Enables accurate and consistent results

View a selection guide for all fixable viability dyes for flow cytometry.

Ready-to-use control
Unlike other methods that require sample preparation to make compensation controls using cellular material, the ArC Amine Reactive Compensation Bead Kit is ready to use out of the dropper bottle. The kit includes two types of specially modified polystyrene microspheres that have been optimized to react with the amine-reactive dye in the LIVE/DEAD Fixable dead cell stain kits. The ArC reactive beads (Component A) bind any of the amine-reactive dyes and provide a positive signal; the ArC negative beads (Component B) have no reactivity and provide a negative compensation control. This ready-to-use product preserves the original sample material for experiments; precious sample is not used for the creation of compensation controls.

Accurate and consistent results
Unlike biological controls, which can have variable expression levels depending upon disease or development state, the Arc beads provide a bright, consistent signal (see figure below). Consistency in the staining pattern of compensation controls is important for obtaining the right compensation value. If the signal varies with the control material used, the compensation value can be affected, leading to erroneous results.

How it works
One drop of beads is added to a test tube containing LIVE/DEAD Fixable dead cell stain. After incubation with amine-reactive dye, the beads are washed in staining buffer, a drop of negative control beads is added (if required), and the beads are resuspended and analyzed by flow cytometry. The two components provide a distinct positive bead that is at least 50-fold brighter than the negative beads, which can be used to set compensation.

Other compensation products
Besides the ArC Amine Reactive Compensation Beads, AbC™ Anti-Mouse Bead Kit is also available for capture of mouse anti-human antibodies, as well as the AbC™ Anti-Rat/Hamster Bead Kit for capture of rat anti-mouse or hamster anti-mouse antibodies.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodFluorescence
Diameter (Metric)6 μm
Excitation Wavelength Rangeany lasers (UV to 633/635)
For Use With (Equipment)Flow Cytometer
FormatTube
No. of Tests100
Quantity1 Kit
Shipping ConditionRoom Temperature
Stain ConfigurationSurface
Product LineCompenFlow, Molecular Probes
Product TypeCompensation Beads
Unit SizeEach
Contents & Storage
Contains 1 vial ArC™ amine reactive beads and 1 vial of negative beads.
  • Store at 2°C to 8°C
  • Frequently asked questions (FAQs)

    Are the vials of ArC Amine Reactive Compensation Bead Kit (for use with LIVE/DEAD Fixable dead cell stain kits) (Cat. No. A10346, A10648) compatible with Vaporized Hydrogen Peroxide (VHP) sterilization?

    While the polypropylene cap is compatible with Vaporized Hydrogen Peroxide (VHP) sterilization, we have not tested the compatibility of the Low-Density Polyethylene (LDPE) / Linear Low-Density Polyethylene (LLDPE) vials with VHP sterilization.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    What is the stability for the ArC Amine Reactive Compensation Bead Kit (for use with LIVE/DEAD Fixable dead cell stain kits)?

    When stored as directed (2-8 degrees C), this kit is stable for at least 1 year. Please do not freeze the kit. Please visit the user guide (https://assets.thermofisher.com/TFS-Assets/LSG/manuals/arc_amine_reactive_comp_bead_kit_man.pdf) for further technical details.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    My ArC Amine Reactive Compensation beads are excessively clumped and cannot be resuspended by vortexing or sonication. What may have caused this?

    This can occur if the solution of beads was ever frozen. The formation of ice excludes the beads and compresses the beads together. Once frozen, the beads cannot be resuspended into solution and are no longer usable.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    For the ArC Amine Reactive Compensation Bead Kit, why must I use freshly prepared amine-reactive dye?

    This is because succinimidyl ester (NHS ester) groups are very labile to water; they dissociate readily from the dye structure if held in solvents that are contaminated with water, as is possible from condensation or absorbing water from the atmosphere.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    Besides the Live/Dead Fixable Dead Cell stain, may I conjugate other amine-reactive dyes to the beads in the ArC Amine Reactive Compensation Bead Kit?

    Yes. The succinimidyl ester (NHS ester) and isothiocyanate (e.g., FITC, TRITC) dye derivatives may be attached to the ArC beads, but you would have to optimize the amount of reactive dye per ArC beads.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    Citations & References (9)

    Citations & References
    Abstract
    IL-1 family members IL-18 and IL-33 upregulate the inflammatory potential of differentiated human Th1 and Th2 cultures.
    Authors:Blom L, Poulsen LK,
    Journal:J Immunol
    PubMed ID:23028054
    'The IL-1 family members IL-1ß, IL-18, and IL-33 are potent cytokines in relationship to amplifying the CD4(+) T cell cytokine production. To evaluate their impact on in vitro-differentiated human Th1 and Th2 cultures, such cultures were established from naive T cells, purified from healthy blood donors, and reactivated in the ... More
    Multiparameter flow cytometry and bioanalytics for B cell profiling in systemic lupus erythematosus.
    Authors:Kaminski DA, Wei C, Rosenberg AF, Lee FE, Sanz I
    Journal:Methods Mol Biol
    PubMed ID:22933067
    B lymphocyte involvement in systemic lupus erythematosus has been recognized for several decades, mainly in the context of autoantibody production. Both mouse and human studies reveal that different types of antibody responses, as well as antibody-independent effector functions can be ascribed to distinct subpopulations (subsets) of circulating B cells. Characterizing ... More
    Evaluation of pneumonia virus of mice as a possible human pathogen.
    Authors:Brock LG, Karron RA, Krempl CD, Collins PL, Buchholz UJ,
    Journal:J Virol
    PubMed ID:22438539
    Pneumonia virus of mice (PVM), a relative of human respiratory syncytial virus (RSV), causes respiratory disease in mice. There is serologic evidence suggesting widespread exposure of humans to PVM. To investigate replication in primates, African green monkeys (AGM) and rhesus macaques (n = 4) were inoculated with PVM by the ... More
    A novel aldehyde dehydrogenase-3 activator leads to adult salivary stem cell enrichment in vivo.
    Authors:Banh A, Xiao N, Cao H, Chen CH, Kuo P, Krakow T, Bavan B, Khong B, Yao M, Ha C, Kaplan MJ, Sirjani D, Jensen K, Kong CS, Mochly-Rosen D, Koong AC, Le QT,
    Journal:Clin Cancer Res
    PubMed ID:21998334
    To assess aldehyde dehydrogenase (ALDH) expression in adult human and murine submandibular gland (SMG) stem cells and to determine the effect of ALDH3 activation in SMG stem cell enrichment. Adult human and murine SMG stem cells were selected by cell surface markers (CD34 for human and c-Kit for mouse) and ... More
    Targeting GLUT1 and the Warburg effect in renal cell carcinoma by chemical synthetic lethality.
    Authors:Chan DA, Sutphin PD, Nguyen P, Turcotte S, Lai EW, Banh A, Reynolds GE, Chi JT, Wu J, Solow-Cordero DE, Bonnet M, Flanagan JU, Bouley DM, Graves EE, Denny WA, Hay MP, Giaccia AJ,
    Journal:Sci Transl Med
    PubMed ID:21813754
    Identifying new targeted therapies that kill tumor cells while sparing normal tissue is a major challenge of cancer research. Using a high-throughput chemical synthetic lethal screen, we sought to identify compounds that exploit the loss of the von Hippel-Lindau (VHL) tumor suppressor gene, which occurs in about 80% of renal ... More