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    AbC Anti-Rat/Hamster Bead Kit

    互联网

    1141

    实验试剂

     

    The AbC™ RH capture beads and negative beads have a diameter of approximately 6 μm (actual size for each lot is listed on the component vial). The bead suspensions are supplied in dropper vials for convenient sample application.

    Table 1. Contents and storage information.

    Material

    Amount

    Composition

    Storagundefined

    Stability

    AbC™ RH capture beads
    (Component A)



    Negative beads (Component B)

    5 mL

    4 × 106 beads/mL in phosphate buffered saline (PBS) with 0.1% BSA and 2 mM sodium azide

    3 × 106 beads/mL in deionized water containing 2 mM sodium azide and 0.05% Tween® 20

    When stored as directed, this kit is stable for at least 1 year.

    		  

    Number of assays: Sufficient material is supplied for 100 assays based on the protocol below.
    Materials Required but Not Provided

    实验步骤

     

    1. Using the AbC™ anti- Rat/Hamster Bead Kit

    1)      Completely resuspend the AbC™ RH capture beads (Component A) and negative beads (Component B) by gently vortexing for 30 seconds before use.

    2)      Label a sample tube for each fluorochrome-conjugated rat or hamster antibody you are using, and add 1 drop of AbC™ RH capture beads (Component A) to each tube.

    3)      Add a pre-titrated amount of each rat or hamster antibody conjugate to the AbC™ RH capture bead suspension in the designated tube and mix well. Make sure to deposit the antibody directly to the bead suspension.

    4)      Incubate for 15 minutes at room temperature, protected from light.

    5)      Add 3 mL of PBS or other buffer to sample tubes. Centrifuge for 5 minutes at 200 × g.

    6)      Carefully remove the supernatant from tubes and resuspend the bead pellet by adding 0.5 mL of PBS or other buffer to sample tubes.

    7)      Add one drop of negative beads (Component B) to the tubes and mix well.

    8)      Vortex tubes before analyzing using flow cytometry. You may briefly sonicate to increase the percentage of singlet beads, if necessary.

    9)      Perform manual or automatic compensation according to the preferred procedure for the flow cytometer in use. Gate on the bead singlet population based on FCS and SSC characteristics.

    2. Combining AbC™ anti-Rat/Hamster and ArC™ Amine Reactive Compensation Bead Kits
    The ArC™ Amine Reactive Compensation Bead Kit (Cat. no. A10346) is designed to facilitate compensation when using any of the LIVE/DEAD® fixable dead cell stains, all amine-reactive dyes. This kit provides two types of specially modified polystyrene microspheres, the ArC™ reactive beads (Component A) that bind any of the amine-reactive dyes, and the ArC™ negative beads (Component B), that have no reactivity. Using the two kit components with any amine-reactive dye will provide distinct positive and negative populations of beads. You can use the AbC™ anti-Rat/Hamster Bead Kit and the ArC™ Amine Reactive Compensation Bead Kit together to calculate compensation in multicolor immunophenotyping experiments that incorporate a LIVE/DEAD® fixable dye by following the protocol outlined below:

          1)      Gently vortex the ArC™ Amine Reactive Beads Kit and the AbC™ anti-Rat/Hamster Bead Kit components for 30 seconds to completely resuspend before use.

    2)      Label a sample tube for the amine-reactive dye you are using, and add 1 drop of ArC™ reactive beads (Component A) to a labeled sample tube. Allow ArC™ reactive beads to sit in the tube for 5 minutes to warm to room temperature.

    3)      Prepare fluorescent reactive dye according to kit instructions included in the LIVE/DEAD® Fixable Dead Cell Stain Kit. For optimal performance of ArC™ reactive beads, always use freshly prepared amine-reactive dye. Do not use previously frozen dye solution.

    4)      Add the amount of LIVE/DEAD® fixable dead cell stain listed in Table 2 to the bead suspension and mix well. Make sure to deposit the amine-reactive dye directly to the bead suspension.

     

    Table 2. Amount of amine-reactive LIVE/DEAD® fixable dead cell stain for use with ArC™ reactive beads.

    Amine-reactive dye for use with ArC™ reactive beads

    Amount

    LIVE/DEAD® Fixable Blue stain

    3 μL

    LIVE/DEAD® Fixable Violet stain

    1 μL

    LIVE/DEAD® Fixable Aqua stain

    3 μL

    LIVE/DEAD® Fixable Yellow stain

    3 μL

    LIVE/DEAD® Fixable Green stain

    3 μL

    LIVE/DEAD® Fixable Red stain

    1 μL

    LIVE/DEAD® Fixable Far Red stain

    3 μL

    LIVE/DEAD® Fixable Near-IR stain

    1 μL

     

    5)      Label another sample tube for each fluorochrome-conjugated antibody you are using, and add 1 drop of AbC™ capture beads (Component A in the AbC™ Anti-Mouse Bead Kit) to each tube.

    6)      Add a pre-titrated amount of antibody conjugate to the appropriate tube and mix well. Make sure to deposit the antibody directly to the bead suspension.

    7)      Incubate for 30 minutes at room temperature, protected from light.

    8)      Add 3 mL of PBS or other buffer to each sample tube. Centrifuge at 300 × g for 5 minutes to collect the beads.

    9)      Carefully remove all supernatant from each tube. If using the red fluorescent reactive dye (Cat. no. L23102), repeat step 8 for that tube.

    10)  Resuspend the bead pellet by adding 0.5 mL of buffer to each sample tube.

    11)  Add one drop of negative beads (Component B in the AbC™ Anti-Mouse Bead Kit) to sample tube(s) containing the AbC™ capture beads.

    12)  Add one drop of ArC™ negative beads (Component B in the ArC™ Amine Reactive Compensation Bead Kit ) to sample tube(s) containing the ArC™ reactive beads.

    13)  Vortex tubes before analyzing using flow cytometry.

    14)  Perform manual or automatic compensation according to the preferred procedure for the flow cytometer in use. Gate on the bead singlet population based on FSC and SSC characteristics.

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