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picolorlock gold colorimetric assay kit  (Novus Biologicals)


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    Structured Review

    Novus Biologicals picolorlock gold colorimetric assay kit
    A–C, Western blotting analyses of Drp1 phosphorylation (Ser616, Ser637) and mitochondrial location of total Drp1, at ischemic reperfusion day 3 after GCI, using mitochondrial protein samples from CA1 subregion. D, Drp1 GTPase activity in hippocampal CA1 protein samples was quantified using a <t>PiColorLock</t> Gold kit. E, Total mitochondrial fragmentation in CA1 pyramidal neurons from sham, vehicle (Veh) and Mdivi-1 treated animals was examined 3 d after GCI. F, Typical staining of NeuN in vehicle (a) and Mdivi-1 (b) treated animals at day 14 after GCI, and the quantitative analyses of the numbers of surviving neurons in hippocampal CA1 layer (c). Dashed line represents percent value in sham control. Scale bar: 50 μm. Data are presented as means ± SE, n = 4-5 in A-E, n = 8-12 in F. *P < 0.05 versus sham control, #P < 0.05 versus GCI or GCI + sham PBM group. $P < 0.05 versus vehicle treated group.
    Picolorlock Gold Colorimetric Assay Kit, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 83 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/picolorlock+gold+colorimetric+assay+kit/pmc06310117-139-65-71?v=Novus+Biologicals
    Average 94 stars, based on 83 article reviews
    picolorlock gold colorimetric assay kit - by Bioz Stars, 2026-07
    94/100 stars

    Images

    1) Product Images from "Photobiomodulation for Global Cerebral Ischemia: Targeting Mitochondrial Dynamics and Functions"

    Article Title: Photobiomodulation for Global Cerebral Ischemia: Targeting Mitochondrial Dynamics and Functions

    Journal: Molecular neurobiology

    doi: 10.1007/s12035-018-1191-9

    A–C, Western blotting analyses of Drp1 phosphorylation (Ser616, Ser637) and mitochondrial location of total Drp1, at ischemic reperfusion day 3 after GCI, using mitochondrial protein samples from CA1 subregion. D, Drp1 GTPase activity in hippocampal CA1 protein samples was quantified using a PiColorLock Gold kit. E, Total mitochondrial fragmentation in CA1 pyramidal neurons from sham, vehicle (Veh) and Mdivi-1 treated animals was examined 3 d after GCI. F, Typical staining of NeuN in vehicle (a) and Mdivi-1 (b) treated animals at day 14 after GCI, and the quantitative analyses of the numbers of surviving neurons in hippocampal CA1 layer (c). Dashed line represents percent value in sham control. Scale bar: 50 μm. Data are presented as means ± SE, n = 4-5 in A-E, n = 8-12 in F. *P < 0.05 versus sham control, #P < 0.05 versus GCI or GCI + sham PBM group. $P < 0.05 versus vehicle treated group.
    Figure Legend Snippet: A–C, Western blotting analyses of Drp1 phosphorylation (Ser616, Ser637) and mitochondrial location of total Drp1, at ischemic reperfusion day 3 after GCI, using mitochondrial protein samples from CA1 subregion. D, Drp1 GTPase activity in hippocampal CA1 protein samples was quantified using a PiColorLock Gold kit. E, Total mitochondrial fragmentation in CA1 pyramidal neurons from sham, vehicle (Veh) and Mdivi-1 treated animals was examined 3 d after GCI. F, Typical staining of NeuN in vehicle (a) and Mdivi-1 (b) treated animals at day 14 after GCI, and the quantitative analyses of the numbers of surviving neurons in hippocampal CA1 layer (c). Dashed line represents percent value in sham control. Scale bar: 50 μm. Data are presented as means ± SE, n = 4-5 in A-E, n = 8-12 in F. *P < 0.05 versus sham control, #P < 0.05 versus GCI or GCI + sham PBM group. $P < 0.05 versus vehicle treated group.

    Techniques Used: Western Blot, Phospho-proteomics, Activity Assay, Staining, Control



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    Novus Biologicals picolorlock gold colorimetric assay kit
    A–C, Western blotting analyses of Drp1 phosphorylation (Ser616, Ser637) and mitochondrial location of total Drp1, at ischemic reperfusion day 3 after GCI, using mitochondrial protein samples from CA1 subregion. D, Drp1 GTPase activity in hippocampal CA1 protein samples was quantified using a <t>PiColorLock</t> Gold kit. E, Total mitochondrial fragmentation in CA1 pyramidal neurons from sham, vehicle (Veh) and Mdivi-1 treated animals was examined 3 d after GCI. F, Typical staining of NeuN in vehicle (a) and Mdivi-1 (b) treated animals at day 14 after GCI, and the quantitative analyses of the numbers of surviving neurons in hippocampal CA1 layer (c). Dashed line represents percent value in sham control. Scale bar: 50 μm. Data are presented as means ± SE, n = 4-5 in A-E, n = 8-12 in F. *P < 0.05 versus sham control, #P < 0.05 versus GCI or GCI + sham PBM group. $P < 0.05 versus vehicle treated group.
    Picolorlock Gold Colorimetric Assay Kit, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/picolorlock+gold+colorimetric+assay+kit/pmc06310117-139-65-71?v=Novus+Biologicals
    Average 94 stars, based on 1 article reviews
    picolorlock gold colorimetric assay kit - by Bioz Stars, 2026-07
    94/100 stars
      Buy from Supplier

    Image Search Results


    Journal: iScience

    Article Title: RAD51 separation of function mutation disables replication fork maintenance but preserves DSB repair

    doi: 10.1016/j.isci.2024.109524

    Figure Lengend Snippet:

    Article Snippet: PiColorLock Gold Colorimetric Assay Kit , Innova Biosciences , Cat# 303-0030.

    Techniques: Virus, Recombinant, Electron Microscopy, Protease Inhibitor, Western Blot, Plasmid Preparation, Staining, Colorimetric Assay, Sequencing, Expressing, Mutagenesis, Software, Imaging

    A–C, Western blotting analyses of Drp1 phosphorylation (Ser616, Ser637) and mitochondrial location of total Drp1, at ischemic reperfusion day 3 after GCI, using mitochondrial protein samples from CA1 subregion. D, Drp1 GTPase activity in hippocampal CA1 protein samples was quantified using a PiColorLock Gold kit. E, Total mitochondrial fragmentation in CA1 pyramidal neurons from sham, vehicle (Veh) and Mdivi-1 treated animals was examined 3 d after GCI. F, Typical staining of NeuN in vehicle (a) and Mdivi-1 (b) treated animals at day 14 after GCI, and the quantitative analyses of the numbers of surviving neurons in hippocampal CA1 layer (c). Dashed line represents percent value in sham control. Scale bar: 50 μm. Data are presented as means ± SE, n = 4-5 in A-E, n = 8-12 in F. *P < 0.05 versus sham control, #P < 0.05 versus GCI or GCI + sham PBM group. $P < 0.05 versus vehicle treated group.

    Journal: Molecular neurobiology

    Article Title: Photobiomodulation for Global Cerebral Ischemia: Targeting Mitochondrial Dynamics and Functions

    doi: 10.1007/s12035-018-1191-9

    Figure Lengend Snippet: A–C, Western blotting analyses of Drp1 phosphorylation (Ser616, Ser637) and mitochondrial location of total Drp1, at ischemic reperfusion day 3 after GCI, using mitochondrial protein samples from CA1 subregion. D, Drp1 GTPase activity in hippocampal CA1 protein samples was quantified using a PiColorLock Gold kit. E, Total mitochondrial fragmentation in CA1 pyramidal neurons from sham, vehicle (Veh) and Mdivi-1 treated animals was examined 3 d after GCI. F, Typical staining of NeuN in vehicle (a) and Mdivi-1 (b) treated animals at day 14 after GCI, and the quantitative analyses of the numbers of surviving neurons in hippocampal CA1 layer (c). Dashed line represents percent value in sham control. Scale bar: 50 μm. Data are presented as means ± SE, n = 4-5 in A-E, n = 8-12 in F. *P < 0.05 versus sham control, #P < 0.05 versus GCI or GCI + sham PBM group. $P < 0.05 versus vehicle treated group.

    Article Snippet: The beads were washed four times with GTPase wash buffer (50 mM Tris-HCl, pH 7.5, 1.0 M NaCl, 10 mM MgCl2, 4 mM DTT, 1 mM PMSF) and incubated with 0.5 mM GTP in reaction buffer (50 mM Tris-HCl, pH 7.5, 50 mM NaCl, 20 mM EDTA, and 5 mM MgCl2) at 30° C for 1 h. The released free phosphate was measured using a PiColorLock Gold Colorimetric Assay Kit (#303-0030, Novus Biologicals) according to the kit booklet protocol.

    Techniques: Western Blot, Phospho-proteomics, Activity Assay, Staining, Control