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Phrodo s aureus bioparticles

Manufactured by Thermo Fisher Scientific

The PHrodo S. aureus BioParticles is a fluorescent labeling reagent designed for the detection and analysis of Staphylococcus aureus bacteria. The product provides a quantitative measurement of S. aureus interaction with host cells or other biological targets.

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2 protocols using phrodo s aureus bioparticles

1

Quantitative Phagocytosis Assay Using pHrodo S. aureus

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Phagocytosis was assayed via uptake of pHrodo S. aureus BioParticles (Invitrogen, Eugene, OR). BioParticle conjugates are novel, no wash fluorogenic particles that are used for quantitative measurement of phagocytosis. Cells were cultured in complete media for 24 hours at a concentration of 2 × 105 in Mattek tissue culture dishes. BioParticles prepared per manufacturer instructions were added to cells at a 5:1 ratio and cells plus particles incubated at 37°C for 30 minutes to allow for uptake. Cells were washed to remove unattached BioParticles, fixed in 2% paraformalin, stained with Alexa-488 conjugated anti-MR antibody, and prepared for confocal microscopy. Samples were examined by confocal microscopy using anti-MR Alexa-488, or Alexa 647-conjugated antibody against anti-TLR2 or Rab antibodies.
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2

Quantitative Phagocytosis Assay Using pHrodo S. aureus

Check if the same lab product or an alternative is used in the 5 most similar protocols
Phagocytosis was assayed via uptake of pHrodo S. aureus BioParticles (Invitrogen, Eugene, OR). BioParticle conjugates are novel, no wash fluorogenic particles that are used for quantitative measurement of phagocytosis. Cells were cultured in complete media for 24 hours at a concentration of 2 × 105 in Mattek tissue culture dishes. BioParticles prepared per manufacturer instructions were added to cells at a 5:1 ratio and cells plus particles incubated at 37°C for 30 minutes to allow for uptake. Cells were washed to remove unattached BioParticles, fixed in 2% paraformalin, stained with Alexa-488 conjugated anti-MR antibody, and prepared for confocal microscopy. Samples were examined by confocal microscopy using anti-MR Alexa-488, or Alexa 647-conjugated antibody against anti-TLR2 or Rab antibodies.
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