MojoSort™ Human Pan DC Isolation Kit Column Protocol

 

Introduction

 

BioLegend MojoSort™ nanobeads work in commonly used separation columns, based on our internal research as well as validation by external testing by academic labs. This simple protocol consists of following the MojoSort™ protocol to label the cells with pre-diluted MojoSort™ reagents and using the columns as indicated by the manufacturer.

Note: Due to the properties of our beads, it may be possible to use far fewer beads that with other commercial suppliers. We recommend a titration to find the best dilution factor. However, as a general rule, dilutions ranging from 1:3 to 1:20 for the Nanobeads can be used. Please contact BioLegend Technical Service (tech@biolegend.com) if further assistance is needed.

Important Note

 

MojoSort™ magnetic particles can be used with other commercially available magnetic separators, both free standing magnets and column-based systems. Because MojoSort™ protocols are optimized for the MojoSort™ separator, the protocols may need to be adjusted for other systems. Please contact BioLegend Technical Service (tech@biolegend.com) for more information and guidance. We do not recommend using MojoSort™ particles for BD’s IMag™ or Life Technologies’ DynaMag™.

 

Protocol Steps

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1. Prepare cells from your tissue of interest or blood without lysing erythrocytes.  


2. In the final wash of your sample preparation, resuspend the cells in MojoSort™ Buffer by adding up to 4 mL in a 5 mL (12 x 75 mm) polypropylene tube.
   Note: Keep MojoSort™ Buffer on ice throughout the procedure.  


3. Filter the cells with a 70µm cell strainer, centrifuge at 300xg for 5 minutes, and resuspend in an appropriate volume of MojoSort™ Buffer. Count and adjust the cell concentration to 1 x 10⁸ cells/mL.


4. Aliquot 100µL of cell suspension (10⁷ cells) into a new tube. Add 10µL Human TruStain FcX™. Mix well and incubate at room temperature for 10 minutes. Scale up the volume accordingly if separating more cells. For example, if the volume of Human TruStain FcX™ for 1x10⁷ cells is 10µL, add 100µL for 1 x 10⁸ cells. When working with less than 10⁷ cells, use indicated volumes for 10⁷ cells.


5. To make the pre-diluted biotin, mix 10µL of the Biotin-Antibody Cocktail with 30µL of 1X MojoSort™ Buffer. Add 10µL of this pre-diluted Biotin-Antibody Cocktail. Mix well and incubate on ice for 15 minutes. Scale up the volume if separating more cells. For example, add 100µL of pre-diluted Antibody Cocktail for separating 1 x 10⁸ cells in 1mL of MojoSort™ Buffer. When working with less than 10⁷ cells, use indicated volumes for 10⁷ cells.


6. Vortex the Streptavidin Nanobeads (to resuspend) at max speed, 5 touches. Prepare the nanobead dilution by mixing 20µL of Streptavidin Nanobeads with 80µL of 1X MojoSort™ Buffer. Add 20µL of pre-diluted Streptavidin Nanobeads. Mix well and incubate on ice for 15 minutes. Scale up the volume accordingly if separating more cells. For example, add 200 µL of pre-diluted Nanobeads for separating 1 x 10⁸ cells in 1 mL of MojoSort™ Buffer. When working with less than 10⁷ cells, use indicated volumes for 10⁷ cells.


7. Wash the cells by adding MojoSort™ Buffer up to 4mL. Centrifuge the cells at 300xg for 5 minutes.


8. Discard the supernatant.


9. Resuspend the cells in appropriate amount of MojoSort™ Buffer and proceed to separation. At least 500µL is needed for column separation.
   Note: There are several types of commercially available columns, depending on your application. Choose the one that fits best your experiment:

Columns:

 

Example of magnetic separation with medium capacity columns:

1. Place the column in a magnetic separator that fits the column.
2. Rinse the column with 3 mL of cell separation buffer.
3. Add the labeled cell suspension in at least 500uL of buffer to the column through a 30µm filter and collect the fraction containing the unlabeled cells. These are the cells of interest; do not discard.
4. Wash the cells in the column 2 times with 3mL of buffer and collect the fraction containing the untouched cells. Combine with the collected fraction from step 3.
5. If desired, the labeled cells can be collected by taking away the column from the magnet and place it on a tube. Then add 5 mL of buffer and flush out the magnetically labeled fraction with a plunger or supplied device. The labeled cells may be useful as staining controls, to monitor purity/yield, or other purposes.

 

Data

 

Flow cytometry. High purity and yield. “After Isolation” plot shows purified population of interest using pre-diluted MojoSort™ reagents in separation columns.

 

 

 

Kit	Purity	Yield
Mouse CD4 T Cell Isolation Kit	95.7%	85%

 

 

Electron Microscopy. CD4⁺ T cells Isolated with MojoSort™ CD4 T Cell Isolation Kit using columns do not display particles in the cell surface. Image is representative of 36 different cells.

CD4+ T cells isolated with MojoSort™ CD4 T Cell Isolation Kit using separation columns.

 

General Tips & FAQ

 

What dilution of the reagents shall I use?

Dilutions are lot dependent please contact tech@biolegend.com for recommended dilution.