- Other Names
- Mouse CD90.2 Positive Selection, CD90.2 Positive selection
- Ave. Rating
- 0 reviews
- Product Citations
|Cat #||Size||Price||Quantity Avail.||Save|
Mouse CD90.2+ cells are either selected or depleted by incubating the sample with biotin conjugated anti-mouse CD90.2 antibody followed by Streptavidin Nanobeads. The magnetically labeled fraction is retained by the use of a magnetic separator. After collection of the CD90.2+ expressing cells, downstream applications include functional assays, gene expression, phenotypic characterization, etc.Product Details
- Kit Contents
For Cat. No. 480101:
- 1 vial containing 200 µl of Biotin anti-mouse CD90.2 antibody (clone 30-H12)
- 1 vial containing 200 µl Streptavidin Nanobeads
For Cat# 480102:
- 2 vials containing 1 ml each of Biotin anti-mouse CD90.2 antibody (clone 30-H12)
- 2 vials containing 1 ml each of Streptavidin Nanobeads
Cocktail: Phophate buffer solution containing 0.09% sodium azide, 0.5% BSA, pH 7.2.
Streptavidin Nanobeads: Aqueous solution containing 0.05% sodium azide and 0.3% BSA.
The antibodies were purified by affinity chromatography, and conjugated wtih biotin under optimal conditions. The solution is free of unconjugated biotin.
Streptavidin Nanobeads: protein-coated magnetic nanobeads.
- Storage & Handling
- Antibody cocktail and Streptavidin Nanobeads should be stored undiluted between 2°C and 8°C.
Cell Separation (MojoSort™) - Quality tested
- Recommended Usage
Volume of Streptavidin Nanobeads should be adjusted depending on starting percentage of CD90.2+ cells to be isolated. Use the table below as an example when working with a cell mixture of C57BL/6 (CD90.2+) and FVB/NJ (CD90.2-) mice. For 1x107 cells in 100 µl of buffer, use the following volumes:
C57BL/6 + FVB/NJ Mixture (spleen)
Starting CD90.2 Frequency
Optimal Nanobeads Volume
10% C57BL/6 + 90% FVB/NJ
25% C57BL/6 + 75% FVB/NJ
50% C57/BL/6 + 50% FVB/NJ
75% C57BL/6 + 25% FVB/NJ
The volumes indicated in the table are for the use of MojoSort™ magnet (Cat. No. 480019/480020). For low frequency cells, pre-dilute the Streptavidin Nanobeads in order to pipette a minimum of 5 µl of any solution. For example, to isolate CD90.2+ cells from a mixture of 25% C57BL/6 and 75% FVB/NJ, pre-dilute 10 µl of Streptavidin Nanobeads in 90 µl of MojoSort™ buffer (Cat. No. 480017) and add 7.7 µl of that dilution per sample. Avoid working with small volumes.
- Application Notes
This kit is designed for the positive selection or depletion of mouse CD90.2+ cells from lymphoid tissue.
Each lot has been individually optimized. Do not mix and match components from different lots or different kits.
To find out the dilution to use this product in separation columns please download the CoA.
- Are MojoSort™ Nanobeads compatible with other commercially available magnetic separation systems?
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 for more information and guidance. We do not recommend using MojoSort™ particles for BD’s IMag™ or Life Technologies’ DynaMag™.
- Can your magnetic particles be sterile filtered?
Yes, they can be sterile filtered as the particles are smaller than 0.22 µm.
- Is there a way to detach your magnetic particles from the cell surface?
No, not currently. We have found that cells are functional without the need to detach the magnetic Nanobeads.
- What is the size of your magnetic particles?
The average diameter is approximately 130 nm.