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SYGNIS AG picolorlock gold phosphate detection kit
Picolorlock Gold Phosphate Detection Kit, supplied by SYGNIS AG, 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/picolorlock+gold+phosphate+detection+kit/picolorlock+gold+phosphate+detection+system/pm39121859-605-10-17
Average 90 stars, based on 1 article reviews
picolorlock gold phosphate detection kit - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

other:

Article Title: Binding and/or hydrolysis of purine-based nucleotides is not required for IM30 ring formation.
Article Snippet: Finally, 20 μL of “stabilizer” (PiColorLock Gold Phosphate Detection Kit by Innova Biosciences) was added.

Activity Assay:

Article Title: Development of a mitochondria-targeted Hsp90 inhibitor based on the crystal structures of human TRAP1.
Article Snippet: The mitochondrial pool of Hsp90 and its mitochondrial paralogue, TRAP1, suppresses cell death and reprograms energy metabolism in cancer cells; therefore, Hsp90 and TRAP1 have been suggested as target proteins for anticancer drug development.. Here, we report that the actual target protein in cancer cell mitochondria is TRAP1, and current Hsp90 inhibitors cannot effectively inactivate TRAP1 because of their insufficient accumulation in the mitochondria.. To develop mitochondrial TRAP1 inhibitors, we determined the crystal structures of human TRAP1 complexed with Hsp90 inhibitors.

Article Title: Dual Binding to Orthosteric and Allosteric Sites Enhances the Anticancer Activity of a TRAP1-Targeting Drug.
Article Snippet: Subscriber access provided by University of Texas Libraries is published by the American Chemical Society.. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society.. Copyright © American Chemical Society.

Article Title: Development of pyrazolo[3,4-d]pyrimidine-6-amine-based TRAP1 inhibitors that demonstrate in vivo anticancer activity in mouse xenograft models.
Article Snippet: TNF Receptor Associated Protein 1 (TRAP1) is a mitochondrial paralog of Hsp90 related to the promotion of tumorigenesis in various cancers via maintaining mitochondrial integrity, reducing the production of reactive oxygen species, and reprogramming cellular metabolism.. Consequently, Hsp90 and TRAP1 have been targeted to develop cancer therapeutics.. Herein, we report a series of pyrazolo[3,4-d]pyrimidine derivatives that are mitochondria-permeable TRAP1 inhibitors.

Clinical Proteomics:

Article Title: Antisense oligonucleotides enhance SLC20A2 expression and suppress brain calcification in a humanized mouse model.
Article Snippet: In brief Zhao et al. discover that mRNA and protein expression of phosphate importer SLC20A2 is compromised by intronic mutations, which resulted in increased cryptic-exon incorporation.. Spliceswitching ASOs targeting cryptic exons restore SLC20A2 expression and brain phosphate homeostasis and suppress brain calcification, providing a therapeutic strategy for PFBC patients with SLC20A2 haploinsufficiency.

Spectrophotometry:

Article Title: Antisense oligonucleotides enhance SLC20A2 expression and suppress brain calcification in a humanized mouse model.
Article Snippet: In brief Zhao et al. discover that mRNA and protein expression of phosphate importer SLC20A2 is compromised by intronic mutations, which resulted in increased cryptic-exon incorporation.. Spliceswitching ASOs targeting cryptic exons restore SLC20A2 expression and brain phosphate homeostasis and suppress brain calcification, providing a therapeutic strategy for PFBC patients with SLC20A2 haploinsufficiency.



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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.
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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