Review



blue fluorescent bead motility hitkit  (Thermo Fisher)


Bioz Verified Symbol Thermo Fisher is a verified supplier
Bioz Manufacturer Symbol Thermo Fisher manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 90
      Buy from Supplier

    Structured Review

    Thermo Fisher blue fluorescent bead motility hitkit
    Blue Fluorescent Bead Motility Hitkit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/pmc01173138-193-9-13
    Average 90 stars, based on 1 article reviews
    blue fluorescent bead motility hitkit - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Migration:

    Article Title: RhoC GTPase is required for PC-3 prostate cancer cell invasion but not motility.
    Article Snippet: .. Motility, migration, haptotaxis and invasion assays Random motility assays were also performed using blue fluorescent bead motility HitKit (Cellomics, Pittsburg, PA, USA), which is based on the colloidal gold random motility assay (Albrecht-Buehler, 1977; van Golen et al., 2000a, b). .. Cells, 200/well in SFM, were seeded onto a lawn of blue fluorescent beads in a BSA-coated 96-well plate (BD Biosciences).

    Article Title: Regulation of pancreatic cancer cell migration and invasion by RhoC GTPase and Caveolin-1
    Article Snippet: .. Random migration assays were also performed using the blue fluorescent bead motility HitKit (Cellomics, Pittsburg, PA). .. Cells, 200/well in serum free medium (SFM), were seeded onto a lawn of blue fluorescent beads in a BSA coated 96-well plate (BD Biosciences, San Diego, CA).

    Motility Assay:

    Article Title: RhoC GTPase is required for PC-3 prostate cancer cell invasion but not motility.
    Article Snippet: .. Motility, migration, haptotaxis and invasion assays Random motility assays were also performed using blue fluorescent bead motility HitKit (Cellomics, Pittsburg, PA, USA), which is based on the colloidal gold random motility assay (Albrecht-Buehler, 1977; van Golen et al., 2000a, b). .. Cells, 200/well in SFM, were seeded onto a lawn of blue fluorescent beads in a BSA-coated 96-well plate (BD Biosciences).



    Similar Products

    hitkit  (Thermo Fisher)
    86
    Thermo Fisher hitkit
    Hitkit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/pmc03164618-33-0-12
    Average 86 stars, based on 1 article reviews
    hitkit - by Bioz Stars, 2026-10
    86/100 stars
    		  Buy from Supplier
    multiparameter apoptosis hitkit  (Thermo Fisher)
    90
    Thermo Fisher multiparameter apoptosis hitkit
    The effects of TXS inhibition on tumour cell <t>apoptosis</t> . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).
    Multiparameter Apoptosis Hitkit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/pmc03074522-200-1-5
    Average 90 stars, based on 1 article reviews
    multiparameter apoptosis hitkit - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier
    blue fluorescent bead motility hitkit  (Thermo Fisher)
    90
    Thermo Fisher blue fluorescent bead motility hitkit
    The effects of TXS inhibition on tumour cell <t>apoptosis</t> . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).
    Blue Fluorescent Bead Motility Hitkit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/pmc01173138-193-9-13
    Average 90 stars, based on 1 article reviews
    blue fluorescent bead motility hitkit - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier
    hitkit hcs reagent kit  (Thermo Fisher)
    86
    Thermo Fisher hitkit hcs reagent kit
    The effects of TXS inhibition on tumour cell <t>apoptosis</t> . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).
    Hitkit Hcs Reagent Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/us10376514-917-5-9
    Average 86 stars, based on 1 article reviews
    hitkit hcs reagent kit - by Bioz Stars, 2026-10
    86/100 stars
    		  Buy from Supplier
    hitkit™ hcs reagent kit  (Thermo Fisher)
    90
    Thermo Fisher hitkit™ hcs reagent kit
    The effects of TXS inhibition on tumour cell <t>apoptosis</t> . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).
    Hitkit™ Hcs Reagent Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/us09956224-1065-5-9
    Average 90 stars, based on 1 article reviews
    hitkit™ hcs reagent kit - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier
    hitkit oxidative stress kit  (Thermo Fisher)
    90
    Thermo Fisher hitkit oxidative stress kit
    The effects of TXS inhibition on tumour cell <t>apoptosis</t> . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).
    Hitkit Oxidative Stress Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/hitkit+oxidative+stress+kit/pm26647827-62-1-5
    Average 90 stars, based on 1 article reviews
    hitkit oxidative stress kit - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier
    nf-κb activation hitkit™  (Thermo Fisher)
    90
    Thermo Fisher nf-κb activation hitkit™
    The effects of TXS inhibition on tumour cell <t>apoptosis</t> . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).
    Nf κb Activation Hitkit™, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/10__3390_slash_molecules21040465-257-7-10
    Average 90 stars, based on 1 article reviews
    nf-κb activation hitkit™ - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier
    cell motility hitkit  (Thermo Fisher)
    90
    Thermo Fisher cell motility hitkit
    The effects of TXS inhibition on tumour cell <t>apoptosis</t> . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).
    Cell Motility Hitkit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hitkit/us09062341-13-21-24
    Average 90 stars, based on 1 article reviews
    cell motility hitkit - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    The effects of TXS inhibition on tumour cell apoptosis . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).

    Journal: Molecular Cancer

    Article Title: Examination of thromboxane synthase as a prognostic factor and therapeutic target in non-small cell lung cancer

    doi: 10.1186/1476-4598-10-25

    Figure Lengend Snippet: The effects of TXS inhibition on tumour cell apoptosis . A) Apoptosis was induced in a dose-dependant manner following 24 h treatment with ozagrel, relative to untreated control cells. Cell health following ozagrel treatment was assessed using 3 spectrally distinct flourophores to examine nuclei, f -actin (marker of cytoskeletal integrity), and mitochondrial mass/potential. Reduced f -actin levels demonstrate a loss in cellular integrity during apoptosis. Membrane blebbing also occurs and mitochondrial activity occurs, coupled with a loss of potential across the mitochondrial membrane. These markers were quantified by the Kinetic Scan HCS reader and are represented (B). Similar observations were made in SKMES-1 cells (data not shown). Apoptosis was confirmed following selective TXS inhibition by Cell Death Detection ELISA and DNA laddering in both cell lines (A-549 shown as representative). Cell Death ELISA demonstrated increased apoptosis in a concentration dependant manner, with fold induction expressed as a ratio of control cells (C). DNA laddering was also observed following ozagrel treatment at both 500 nM and 5 μM concentrations (D).

    Article Snippet: The Multiparamater Apoptosis HitKit from Cellomics provides High Content Screening qualified fluorescent reagents for simultaneous measurement of 3 fundamental parameters of apoptosis.

    Techniques: Inhibition, Marker, Activity Assay, Enzyme-linked Immunosorbent Assay, DNA Laddering, Concentration Assay

    Effect of stable TXS -over-expression on tumour cell survival . Apoptosis was measured in TXS stable transfectants, and corresponding controls (wild-type and empty vector) following 48 h (A) and 72 h (B) serum-starvation by flow cytometry. Representative dot plots following 72 h serum starvation are shown for wild-type (C), empty vector (D) and TXS overexpressing (E) cells. Graphical data is represented at a percentage of the empty vector control, which was set to 100%. Data is expressed as mean ± SEM. n=3 independent experiments.

    Journal: Molecular Cancer

    Article Title: Examination of thromboxane synthase as a prognostic factor and therapeutic target in non-small cell lung cancer

    doi: 10.1186/1476-4598-10-25

    Figure Lengend Snippet: Effect of stable TXS -over-expression on tumour cell survival . Apoptosis was measured in TXS stable transfectants, and corresponding controls (wild-type and empty vector) following 48 h (A) and 72 h (B) serum-starvation by flow cytometry. Representative dot plots following 72 h serum starvation are shown for wild-type (C), empty vector (D) and TXS overexpressing (E) cells. Graphical data is represented at a percentage of the empty vector control, which was set to 100%. Data is expressed as mean ± SEM. n=3 independent experiments.

    Article Snippet: The Multiparamater Apoptosis HitKit from Cellomics provides High Content Screening qualified fluorescent reagents for simultaneous measurement of 3 fundamental parameters of apoptosis.

    Techniques: Over Expression, Plasmid Preparation, Flow Cytometry