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DynaGreen Protein A/G Magnetic Beads are intended for use in immunoprecipitation (IP) applications while also being an environmentally sustainable choice.
The Magnetic Stand-96 is designed for paramagnetic bead precipitation from standard 96-well, U-bottom microplates and 0.2 mL PCR plates with no additional accessories.
When you wish to covalently couple antibodies, peptides, intact proteins, and functional enzymes to the surface of a magnetic bead choose Dynabeads Tosylactivated.
The Dynabeads Protein G IP Kit and Magnet Starter Pack combines Dynabeads Protein G magnetic beads for immunoprecipitation (including the required buffers) and the magnet preferred for use with 1.5 mL microcentrifuge tubes for purchasing convenience.
DynaGreen CaptureSelect Anti-IgG-Fc (Multi-Species) Magnetic Beads enable high-performance direct and indirect immunoprecipitation (IP) while also being an environmentally sustainable choice.
DynaGreen CaptureSelect Anti-IgG-Fc (Multi-Species) Magnetic Beads are supplied in phosphate buffer, pH 7.4, with a biodegradable surfactant and a preservative. Store at 2–8°C.
For use with Dynabeads ranging from 1–4.5 μm in diameter. Features six bar magnets and is compatible with most 96-well skirted PCR-plates, culture plates, 96-well round bottom plates, 96-well flat bottom plates, 24-well plates, 12-well plates, and 6-well plates.
The Pierce High-Capacity Protein A MagBeads, Alkali Stable are a high-performance magnetic bead for purifying antibodies from cell culture supernatant, ascites, serum, and crude extracts.
Dynabeads Sequential Protein Binding Beads are hydrophobic 2.8 μm monosized Dynabeads magnetic beads optimized for high binding capacity of proteins from lysate for western or mass spectrometry analysis. The beads can be used with Sequential Lysis Buffer, Sequential Protein Bind/Wash Solution, and the Sequential Protein Elution Buffer. It is a component of the Sequential Protein/DNA/RNA Extraction Kit (Cat. No. 50000D).
Thermo Scientific™ Pierce™ Protein A/G Magnetic Agarose Beads provide a fast, convenient method for purification of immunoglobulins from serum, cell culture supernatant, or ascites
These are hydrophilic Dynabeads™ (2.8 μm) with carboxylic acid groups. These surface groups allow covalent amide bond formation to proteins/peptides via primary amino- or sulphydryl groups.
These are hydrophilic Dynabeads™ (2.8 μm) with amine groups. The surface amino groups allow direct covalent binding of carbohydrates, glycoproteins and glycolipids through reductive amination of aldehydes.