The largest database of trusted experimental protocols

Yellow green neutravidin fluorescent beads

Manufactured by Thermo Fisher Scientific
Sourced in United States

Yellow-green neutravidin-fluorescent beads are polystyrene microspheres coated with the protein neutravidin. The beads exhibit yellow-green fluorescence, which can be used for various biological and analytical applications.

Automatically generated - may contain errors

2 protocols using yellow green neutravidin fluorescent beads

1

SARS-CoV-2 Delta Spike Protein Binding Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
This assay was described previously.26 (link) Briefly, biotinylated SARS-CoV-2 Delta spike trimer (ECD; SinoBiological, Beijing, China, cat. no. 40589-V08H10) was incubated with yellow-green neutravidin-fluorescent beads (Molecular Probes, Eugene, OR, USA, cat. no. F8776) for 2 h at 37 °C. 10 μl of a 100-fold dilution of beads–protein was incubated 2 h at 37 °C with 100 μl of diluted plasma (900-fold) before addition of 25,000 cells per well THP-1 cells (RRID:CVCL_0006; Millipore Sigma, Burlington, MA, USA, cat. no. 88081201). After 19 h incubation at 37 °C, the cells were fixed with 2% formaldehyde solution (Tousimis, Rockville MD USA, cat. no. 1008B) and fluorescence was evaluated on a LSRII (BD Bioscience). The phagocytic score was calculated by multiplying the percentage of bead-positive cells by the geometric mean fluorescence intensity (MFI) of the bead-positive cells and dividing by 104.
+ Open protocol
+ Expand
2

SARS-CoV-2 Spike Protein Phagocytosis Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
We measured ADCP as previously described (18 (link)). We incubated biotinylated SARS-CoV-2, SARS-CoV-1, or MERS-CoV S protein with yellow-green neutravidin-fluorescent beads (Molecular Probes-Thermo Fisher Scientific, https://www.thermofisher.com) for 2 h (37°C). We incubated a 100-fold dilution of beads to protein (10 μL) for 2 h at 37°C along with 100 μL of 100-fold diluted plasma before adding THP-1 cells (MilliporeSigma, https://www.sigmaaldrich.com) at 25,000 cells per well. After a 19-h incubation, we fixed cells with 4% formaldehyde solution (Tousimis, https://www.tousimis.com) and evaluated fluorescence on an LSRII (BD Biosciences, https://www.bdbiosciences.com). We calculated the phagocytic score by multiplying the percentage of bead-positive cells by the geometric MFI and dividing by 104.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!