Designed for use with Countess Automated Cell Counter

Designed for use in compensation with all fluorochromes excited by ultraviolet, violet, blue, green, yellow-green, and red lasers. UltraComp eBeads™ react with antibodies of mouse, rat, and hamster origin, and are immunoglobulin light chain-independent. 1 drop (50μL)/test.

Optimized for efficient magnetic separation of all types of Dynabeads; (range 1-4.5μm in diameter) in small (<2mL) sample volumes

For solation and handling of biotinylated nucleic acids, antibodies, or other biotinylated ligands and targets

Excellent for coupling oligos or proteins directly to the beads. Their “cauliflower-like” structure gives Sera-Mag beads high binding capacity. The carboxyl groups on these beads can be activated by standard EDC/EDAC chemistry to react with free amino groups, forming amide bonds.

Optimized to pull all types of Dynabeads (range 1–4.5μm in diameter) to sides of PCR tubes or to sides of wells in 96-well plates

Their “cauliflower-like” structure gives Sera-Mag beads high binding capacity. Sera-Mag Streptavidin beads contain covalently bound streptavidin and are available with low, medium, or high nominal biotin binding capacities. Choose the biotin-binding capacity needed to optimize your application.

Uniform 2.8μm superparamagnetic beads with recombinant Protein G (approximately 17 kDa) covalently coupled to surface

Allows easy coupling of an antibody of your choice to the surface of uniform, 2.8μm superparamagnetic Dynabeads M-270 Epoxy beads

Optimized for efficient magnetic separation of all types of Dynabeads (range 1–4.5μm in diameter) in small sample volumes (1.5mL) in microcentrifuge tubes

Analyze wide size range materials through laser diffraction or other methods with uniform polymer particles that mimic real world particles.

4.5μm superparamagnetic beads with anti-CD3 and anti-CD28 antibodies covalently bound to the bead surface

Spherical particles that can be stained with individual fluorochrome-conjugated antibodies for use as single-color compensation controls. OneComp eBeads react with antibodies of mouse, rat and hamster origin, and are immunoglobulin light chain-independent. 1 drop (50μL)/test

Rapidly isolates mRNA transcriptome in typically 15 minutes, delivering pure, intact mRNA

Optimized to pull all types of Dynabeads to sides in multi-well plates

Covalently couple antibodies, peptides, intact proteins and functional enzymes to surface of magnetic bead

Use with Dynabeads for immunomagnetic separation of cells

For verifying proper functioning of Countess Automated Cell Counter

Minimize contamination by eliminating the need for serial dilutions and extensive sample handling with Thermo Scientific™ COUNT-CAL™ Count Precision Size Standards.

Conveniently check the sizes of bacteria, viruses, ribosomes and sub-cellular components with these size standards.

Ideal solution for assessing multiple protein biomarkers in a single sample. Explore our broad portfolio of pre-configurated panels and combinable single analytes.

Designed for simple and rapid isolation of pure, intact polyadenylated (polyA) mRNA directly from crude lysate of animal and plant cells and tissues

2.8μm superparamagnetic beads containing surface epoxy groups

Designed for use in immunofluorescent staining protocols of cells in suspension. Flow Cytometry Staining Buffer is a buffered saline solution containing fetal bovine serum and sodium azide (0.09%) as a preservative.

For activation and expansion of human T cells

Uniform 2.8μm superparamagnetic beads with recombinant Protein A (approximately 45 kDa) covalently coupled to surface

Alexa Fluor™ 488 Signal-Amplification Kit for Fluorescein- and Oregon Green™ Dye—Conjugated Probes

For confocal and fluorescence microscope calibration

Excellent for coupling oligos or proteins directly to the beads. Their “cauliflower-like” structure gives Sera-Mag beads high binding capacity. The carboxyl groups on these beads can be activated by standard EDC/EDAC chemistry to react with free amino groups, forming amide bonds.

Multilabeled cell preparations for observation by fluorescence microscopy validated for immunofluorescence