
Buffers for use in flow cytometry serve various purposes, including optimizing cellular staining, minimizing non-specific binding, and dilution. Flow cytometry-based cell sorting also employs such buffers. Buffers may contain sodium azide as a preservative and animal serum proteins (such as FBS or BSA) that minimize non-specific binding of antibodies. Buffers that help with cell permeability can comprise of PBS, saponin, and EDTA in addition to a serum protein. Some buffers can also include stains. Fixation buffers can contain paraformaldehyde, and help preserve the light-scattering characteristics and fluorescence staining of cells for use in flow cytometry after immunofluorescence analysis. Some flow cytometry buffers may also contain metabolic inhibitors and antimicrobials. Visit the supplier page for more product information such as quantity and format.
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- Fluorescent antibody conjugates tend to aggregate when in close contact, distorting the analytical results of multicolor...
- 100 Tests
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- Fluorescent antibody conjugates tend to aggregate when in close contact, distorting the analytical results of multicolor...
- 1000 Tests
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- The ReadiUseâ„¢ Annexin Binding Buffer *Optimized for Imaging and Flow Cytometry* is an isotonic buffer ...
- 100 mL
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- The ReadiUseâ„¢ Annexin Binding Buffer *Optimized for Imaging and Flow Cytometry* is an isotonic buffer ...
- 10 mL
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