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streptavidin donor beads  (Revvity)


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    Structured Review

    Revvity streptavidin donor beads
    Streptavidin Donor Beads, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 151 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/streptavidin+donor+beads/Aluminum/us11827642-846-5-8
    Average 91 stars, based on 151 article reviews
    streptavidin donor beads - by Bioz Stars, 2026-10
    91/100 stars

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    Related Articles

    Incubation:

    Article Title: HIV-1 neutralizing antibodies elicited in humans by a prefusion-stabilized envelope trimer form a reproducible class targeting fusion peptide
    Article Snippet: To each well was added 10 μL of biotinylated Env trimer probe at 10 nM final concentration and 10 μL of anti-human Fc IgG (PerkinElmer, Waltham, MA) acceptor beads at 10 μg/mL final concentration. .. The mixtures were incubated at room temperature (RT) for an hour and then added 25 μL of streptavidin donor beads (PerkinElmer, Waltham, MA) at 40 μg/mL final concentration. .. The plate was incubated at RT for 30 min in the dark, and the AlphaLISA signal was read using a SpectraMax i3x multi-mode microplate reader (Molecular Devices, San Jose, CA).

    Article Title: A Cryptic Basic Groove formed by Ubiquitin and Histone H3 Mediates the Selective Recognition of H2AK119Ub Nucleosomes by Synovial Sarcoma X Breakpoint 1 Protein
    Article Snippet: .. 10 μL of 200 nM (or serially diluted) GST-tagged protein (or its mutants) and 10 μL of 12 nM biotinylated nucleosome (or its mutants) were mixed and incubated in OptiPlate-384 microplate (PerkinElmer) for 60 mins, then 10 μL of 20 μg/mL glutathione acceptor beads (PerkinElmer, AL109C, Lot: 2851471) and 10 μL 20 μg/mL streptavidin donor beads (PerkinElmer, 676002S, Lot: 2838642) were added and incubated for another 1 h. Emission at 615nm was detected by Envision plate reader (PerkinElmer). ..

    Article Title: AI-based antibody discovery platform identifies novel, diverse and pharmacologically active therapeutic antibodies against multiple SARS-CoV-2 strains
    Article Snippet: Subsequently, 10 μl of Protein A AlphaLISA ® Acceptor beads (10 μg/ml final concentration; Perkin Elmer cat# AL101C) were added, and further incubated for 1 hour at room temperature in the dark with shaking (250 rpm). .. Following this incubation, 20 μl of Streptavidin Donor beads (40 μg/ml final concentration; Perkin Elmer cat# 6760002S) were added, and the microplates were further incubated for 1 hour at room temperature in the dark with shaking (250 rpm) and read on FLUOStar ® Omega multi-mode microplate reader instrument (BMG Labtech) (excitation 680 nm, emission 615 nm). .. Data were graphed using GraphPad Prism software.

    Article Title: The Parallel Structure–Activity Relationship Screening of Three Compounds Identifies the Common Agonist Pharmacophore of Pyrrolidine Bis-Cyclic Guanidine Melanocortin-3 Receptor (MC3R) Small-Molecule Ligands
    Article Snippet: Briefly, cells 70−90% confluent were dislodged with Versene (Gibco, Waltham, MA, USA) at 37 °C and 10,000 cells/well were plated in a 384-well plate (Optiplate, PerkinElmer, Waltham, MA, USA) with 10 μL of freshly prepared stimulation buffer (1× HBSS, 5 mM HEPES, 0.5 mM IBMX, 0.1% BSA, pH = 7.4) with 0.5 μg of anti-cAMP acceptor beads per well. .. The cells were stimulated with the addition of 5 μL of stimulation buffer containing compound or forskolin (10 −4 M) and incubated in the dark at room temperature for 2 h. Following stimulation, streptavidin donor beads (0.5 μg) and biotinylated cAMP (0.62 μmol) were added to the wells in a green light environment with 10 μL of lysis buffer (5 mM HEPES, 0.3% Tween-20, 0.1% BSA, pH = 7.4) and the plates were incubated in the dark at room temperature for an additional 2 h. Plates were read on a Enspire (PerkinElmer, Waltham, MA, USA) Alpha plate reader using a pre-normalized assay protocol (set by the manufacturer). ..

    Concentration Assay:

    Article Title: HIV-1 neutralizing antibodies elicited in humans by a prefusion-stabilized envelope trimer form a reproducible class targeting fusion peptide
    Article Snippet: To each well was added 10 μL of biotinylated Env trimer probe at 10 nM final concentration and 10 μL of anti-human Fc IgG (PerkinElmer, Waltham, MA) acceptor beads at 10 μg/mL final concentration. .. The mixtures were incubated at room temperature (RT) for an hour and then added 25 μL of streptavidin donor beads (PerkinElmer, Waltham, MA) at 40 μg/mL final concentration. .. The plate was incubated at RT for 30 min in the dark, and the AlphaLISA signal was read using a SpectraMax i3x multi-mode microplate reader (Molecular Devices, San Jose, CA).

    Article Title: AI-based antibody discovery platform identifies novel, diverse and pharmacologically active therapeutic antibodies against multiple SARS-CoV-2 strains
    Article Snippet: Subsequently, 10 μl of Protein A AlphaLISA ® Acceptor beads (10 μg/ml final concentration; Perkin Elmer cat# AL101C) were added, and further incubated for 1 hour at room temperature in the dark with shaking (250 rpm). .. Following this incubation, 20 μl of Streptavidin Donor beads (40 μg/ml final concentration; Perkin Elmer cat# 6760002S) were added, and the microplates were further incubated for 1 hour at room temperature in the dark with shaking (250 rpm) and read on FLUOStar ® Omega multi-mode microplate reader instrument (BMG Labtech) (excitation 680 nm, emission 615 nm). .. Data were graphed using GraphPad Prism software.

    Amplified Luminescent Proximity Homogenous Assay:

    Article Title: Small molecule branched-chain ketoacid dehydrogenase kinase (BDK) inhibitors with opposing effects on BDK protein levels
    Article Snippet: .. Compounds were pre-incubated with BDK prior to the addition of the E2 subunit and signal was developed with the addition of 1:1000 CaptSure tagged Ms Mono anti-DBT antibody (Novus), Anti CaptSure acceptor beads and Streptavidin donor beads at 10 μg/μL in Alpha immunoassay buffer (Perkin Elmer) and read in an EnVision® multilabel reader (Perkin Elmer) using Alphascreen settings. ..

    Article Title: Assay for determining antibody or ligand binding and function
    Article Snippet: .. For the AlphaScreen based method, biotinylated WGA was bound to Streptavidin donor beads (PerkinElmer) and binding of Drozitumab to DR5 was detected with ProtA acceptor beads (PerkinElmer) which bind to the Fc portion of antibodies. ..

    Adhesive:

    Article Title: Compositions useful for treating disorders related to KIT
    Article Snippet: After 90 minutes, 6 ul of 5X AlphaLISA Lysis Buffer (Perkin Elmer) supplemented with a protease and phosphatase inhibitor cocktail (Cell Signaling Technologies) was added to each well and shaken at 450 rpm for 15 minutes at 4° C. 10 ul of phospho-Y719 c-KIT and total c-KIT antibodies (15 nM final concentration, Cell Signaling Technologies) and 50 ug/ml AlphaLISA rabbit acceptor beads (Perkin Elmer) were added to each well and shaken at 300 rpm at room temperature for 2 hours. .. 10 ul of 100 ug/ml streptavidin donor beads (Perkin Elmer) were added to each well, blocked from light with aluminum adhesive and shaken at 300 rpm at room temperature for 2 hours. .. Fluorescence signal was obtained on Envision (Perkin Elmer) by AlphaScreen 384 well HTS protocol.

    Whole Genome Amplification:

    Article Title: Assay for determining antibody or ligand binding and function
    Article Snippet: .. For the AlphaScreen based method, biotinylated WGA was bound to Streptavidin donor beads (PerkinElmer) and binding of Drozitumab to DR5 was detected with ProtA acceptor beads (PerkinElmer) which bind to the Fc portion of antibodies. ..

    Binding Assay:

    Article Title: Assay for determining antibody or ligand binding and function
    Article Snippet: .. For the AlphaScreen based method, biotinylated WGA was bound to Streptavidin donor beads (PerkinElmer) and binding of Drozitumab to DR5 was detected with ProtA acceptor beads (PerkinElmer) which bind to the Fc portion of antibodies. ..

    Lysis:

    Article Title: The Parallel Structure–Activity Relationship Screening of Three Compounds Identifies the Common Agonist Pharmacophore of Pyrrolidine Bis-Cyclic Guanidine Melanocortin-3 Receptor (MC3R) Small-Molecule Ligands
    Article Snippet: Briefly, cells 70−90% confluent were dislodged with Versene (Gibco, Waltham, MA, USA) at 37 °C and 10,000 cells/well were plated in a 384-well plate (Optiplate, PerkinElmer, Waltham, MA, USA) with 10 μL of freshly prepared stimulation buffer (1× HBSS, 5 mM HEPES, 0.5 mM IBMX, 0.1% BSA, pH = 7.4) with 0.5 μg of anti-cAMP acceptor beads per well. .. The cells were stimulated with the addition of 5 μL of stimulation buffer containing compound or forskolin (10 −4 M) and incubated in the dark at room temperature for 2 h. Following stimulation, streptavidin donor beads (0.5 μg) and biotinylated cAMP (0.62 μmol) were added to the wells in a green light environment with 10 μL of lysis buffer (5 mM HEPES, 0.3% Tween-20, 0.1% BSA, pH = 7.4) and the plates were incubated in the dark at room temperature for an additional 2 h. Plates were read on a Enspire (PerkinElmer, Waltham, MA, USA) Alpha plate reader using a pre-normalized assay protocol (set by the manufacturer). ..



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