reference compound Search Results


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Chem Impex International n methyl 2 pyrrolidone nmp
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Chem Impex International tritylchloride resin
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Chem Impex International nanoluc control assays
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Chem Impex International 9 10 phenanthrenequinone
Fluorescence emission spectra (λexc = 532 nm) of mixtures of HDiI and various oxidants. A: Spectra of 1:1 mixtures of HDiI and p-fluoranil (red), p-chloranil (orange), DDQ (light blue), DHAQ (light green), <t>9,10-phenanthrenequinone</t> (light red), DPQ (dark green), and HDiI only (dark blue); the latter four are shown magnified in the inset. B: Commercial DiI only (black), 1:4 HDiI:p-fluoranil (dark red), and HDiI only (blue).
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Chem Impex International compound
Fluorescence emission spectra (λexc = 532 nm) of mixtures of HDiI and various oxidants. A: Spectra of 1:1 mixtures of HDiI and p-fluoranil (red), p-chloranil (orange), DDQ (light blue), DHAQ (light green), <t>9,10-phenanthrenequinone</t> (light red), DPQ (dark green), and HDiI only (dark blue); the latter four are shown magnified in the inset. B: Commercial DiI only (black), 1:4 HDiI:p-fluoranil (dark red), and HDiI only (blue).
Compound, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Chem Impex International uracil 5 monophosphate trisodium chem impex
Fluorescence emission spectra (λexc = 532 nm) of mixtures of HDiI and various oxidants. A: Spectra of 1:1 mixtures of HDiI and p-fluoranil (red), p-chloranil (orange), DDQ (light blue), DHAQ (light green), <t>9,10-phenanthrenequinone</t> (light red), DPQ (dark green), and HDiI only (dark blue); the latter four are shown magnified in the inset. B: Commercial DiI only (black), 1:4 HDiI:p-fluoranil (dark red), and HDiI only (blue).
Uracil 5 Monophosphate Trisodium Chem Impex, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Chem Impex International carboxyphenol ba
Fluorescence emission spectra (λexc = 532 nm) of mixtures of HDiI and various oxidants. A: Spectra of 1:1 mixtures of HDiI and p-fluoranil (red), p-chloranil (orange), DDQ (light blue), DHAQ (light green), <t>9,10-phenanthrenequinone</t> (light red), DPQ (dark green), and HDiI only (dark blue); the latter four are shown magnified in the inset. B: Commercial DiI only (black), 1:4 HDiI:p-fluoranil (dark red), and HDiI only (blue).
Carboxyphenol Ba, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Chem Impex International core solution
Fluorescence emission spectra (λexc = 532 nm) of mixtures of HDiI and various oxidants. A: Spectra of 1:1 mixtures of HDiI and p-fluoranil (red), p-chloranil (orange), DDQ (light blue), DHAQ (light green), <t>9,10-phenanthrenequinone</t> (light red), DPQ (dark green), and HDiI only (dark blue); the latter four are shown magnified in the inset. B: Commercial DiI only (black), 1:4 HDiI:p-fluoranil (dark red), and HDiI only (blue).
Core Solution, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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IsoSciences llc 25-hydroxyvitamin d3
Fluorescence emission spectra (λexc = 532 nm) of mixtures of HDiI and various oxidants. A: Spectra of 1:1 mixtures of HDiI and p-fluoranil (red), p-chloranil (orange), DDQ (light blue), DHAQ (light green), <t>9,10-phenanthrenequinone</t> (light red), DPQ (dark green), and HDiI only (dark blue); the latter four are shown magnified in the inset. B: Commercial DiI only (black), 1:4 HDiI:p-fluoranil (dark red), and HDiI only (blue).
25 Hydroxyvitamin D3, supplied by IsoSciences llc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bachem ac-asp-d-gla-leu-ile-b-cyclohexyl-ala-cyc-oh n-1725.0001
Before cleavage, GFP was found in the plasma membrane (ring shape, before cleavage). Cleavage of the type I MBR by <t>HCV</t> <t>NS3</t> protease resulted in the translocation of GFP to the cytosol (dispersed image, after cleavage).
Ac Asp D Gla Leu Ile B Cyclohexyl Ala Cyc Oh N 1725.0001, supplied by Bachem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Pharmasynth 19 f]fmpep reference standard compound
Before cleavage, GFP was found in the plasma membrane (ring shape, before cleavage). Cleavage of the type I MBR by <t>HCV</t> <t>NS3</t> protease resulted in the translocation of GFP to the cytosol (dispersed image, after cleavage).
19 F]Fmpep Reference Standard Compound, supplied by Pharmasynth, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fluorescence emission spectra (λexc = 532 nm) of mixtures of HDiI and various oxidants. A: Spectra of 1:1 mixtures of HDiI and p-fluoranil (red), p-chloranil (orange), DDQ (light blue), DHAQ (light green), 9,10-phenanthrenequinone (light red), DPQ (dark green), and HDiI only (dark blue); the latter four are shown magnified in the inset. B: Commercial DiI only (black), 1:4 HDiI:p-fluoranil (dark red), and HDiI only (blue).

Journal: ACS applied materials & interfaces

Article Title: Mutually-Reactive, Fluorogenic Hydrocyanine/Quinone Reporter Pairs for In-Solution Biosensing via Nanodroplet Association

doi: 10.1021/acsami.5b10036

Figure Lengend Snippet: Fluorescence emission spectra (λexc = 532 nm) of mixtures of HDiI and various oxidants. A: Spectra of 1:1 mixtures of HDiI and p-fluoranil (red), p-chloranil (orange), DDQ (light blue), DHAQ (light green), 9,10-phenanthrenequinone (light red), DPQ (dark green), and HDiI only (dark blue); the latter four are shown magnified in the inset. B: Commercial DiI only (black), 1:4 HDiI:p-fluoranil (dark red), and HDiI only (blue).

Article Snippet: Activation studies of reduced dye The following quinones were used for re-oxidation studies: p-fluoranil (Alfa Aesar), p-chloranil (Merck KGaA), 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ, Acros Organics), 1,4-dihydroxyanthraquinone, (DHAQ, Acros Organics), 9,10-phenanthrenequinone (Chem-Impex Int’l Inc.), and 3,3′,5,5′-tetra- tert -butyldiphenoquinone (DPQ, TCI Co., Ltd.).

Techniques: Fluorescence

Before cleavage, GFP was found in the plasma membrane (ring shape, before cleavage). Cleavage of the type I MBR by HCV NS3 protease resulted in the translocation of GFP to the cytosol (dispersed image, after cleavage).

Journal: PLoS ONE

Article Title: In-Cell Protease Assay Systems Based on Trans-Localizing Molecular Beacon Proteins Using HCV Protease as a Model System

doi: 10.1371/journal.pone.0059710

Figure Lengend Snippet: Before cleavage, GFP was found in the plasma membrane (ring shape, before cleavage). Cleavage of the type I MBR by HCV NS3 protease resulted in the translocation of GFP to the cytosol (dispersed image, after cleavage).

Article Snippet: A known inhibitor of the HCV NS3 protease, Ac-Asp-D-Gla-Leu-Ile-b-cyclohexyl-Ala-Cyc-OH (N-1725.0001, Bachem, Germany) was purchased and dissolved in dimethyl sulfoxide.

Techniques: Clinical Proteomics, Membrane, Translocation Assay

Type II MBRs were constructed to contain a mitochondrial targeting sequence, MSRA as a masked translocation signal. The masking protein used was GAPDH or GFP for mono- or dual-color type II MBRs, respectively. A . Cleavage of mono-color type II MBR by HCV NS3 protease activates the mitochondrial translocation signal of MSRA, resulting in translocation of GFP from the cytosol (before cleavage) to the mitochondria (after cleavage). B . Cleavage of dual-color type II MBR which contains both GFP and RFP, results in translocation of the RFP from the cytosol (before cleavage) to mitochondria while GFP remains in the cytosol (after cleavage) following cleavage. GFP; green fluorescent protein, RFP; red fluorescent protein.

Journal: PLoS ONE

Article Title: In-Cell Protease Assay Systems Based on Trans-Localizing Molecular Beacon Proteins Using HCV Protease as a Model System

doi: 10.1371/journal.pone.0059710

Figure Lengend Snippet: Type II MBRs were constructed to contain a mitochondrial targeting sequence, MSRA as a masked translocation signal. The masking protein used was GAPDH or GFP for mono- or dual-color type II MBRs, respectively. A . Cleavage of mono-color type II MBR by HCV NS3 protease activates the mitochondrial translocation signal of MSRA, resulting in translocation of GFP from the cytosol (before cleavage) to the mitochondria (after cleavage). B . Cleavage of dual-color type II MBR which contains both GFP and RFP, results in translocation of the RFP from the cytosol (before cleavage) to mitochondria while GFP remains in the cytosol (after cleavage) following cleavage. GFP; green fluorescent protein, RFP; red fluorescent protein.

Article Snippet: A known inhibitor of the HCV NS3 protease, Ac-Asp-D-Gla-Leu-Ile-b-cyclohexyl-Ala-Cyc-OH (N-1725.0001, Bachem, Germany) was purchased and dissolved in dimethyl sulfoxide.

Techniques: Construct, Sequencing, Translocation Assay

The cleavage of type I MBR ( A ) and type II MBR ( B ) by HCV NS3 protease was monitored in the presence of a known peptide derivative inhibitor, Ac-Asp-D-Gla-Leu-Ile-β-cyclohexyl-Ala-Cyc-OH. Both type I and type II MBRs exhibited significant dose-response at nanomolar concentrations.

Journal: PLoS ONE

Article Title: In-Cell Protease Assay Systems Based on Trans-Localizing Molecular Beacon Proteins Using HCV Protease as a Model System

doi: 10.1371/journal.pone.0059710

Figure Lengend Snippet: The cleavage of type I MBR ( A ) and type II MBR ( B ) by HCV NS3 protease was monitored in the presence of a known peptide derivative inhibitor, Ac-Asp-D-Gla-Leu-Ile-β-cyclohexyl-Ala-Cyc-OH. Both type I and type II MBRs exhibited significant dose-response at nanomolar concentrations.

Article Snippet: A known inhibitor of the HCV NS3 protease, Ac-Asp-D-Gla-Leu-Ile-b-cyclohexyl-Ala-Cyc-OH (N-1725.0001, Bachem, Germany) was purchased and dissolved in dimethyl sulfoxide.

Techniques:

An HCV NS3 protease inhibitory RNA aptamer was prepared and tested. Cells co-transfected with vectors encoding type I MBR and HCV NS3 protease were and treated with the RNA aptamer. The inhibition ratio was determined from the number of cells exhibiting a dispersed pattern relative to the total number of cells examined.

Journal: PLoS ONE

Article Title: In-Cell Protease Assay Systems Based on Trans-Localizing Molecular Beacon Proteins Using HCV Protease as a Model System

doi: 10.1371/journal.pone.0059710

Figure Lengend Snippet: An HCV NS3 protease inhibitory RNA aptamer was prepared and tested. Cells co-transfected with vectors encoding type I MBR and HCV NS3 protease were and treated with the RNA aptamer. The inhibition ratio was determined from the number of cells exhibiting a dispersed pattern relative to the total number of cells examined.

Article Snippet: A known inhibitor of the HCV NS3 protease, Ac-Asp-D-Gla-Leu-Ile-b-cyclohexyl-Ala-Cyc-OH (N-1725.0001, Bachem, Germany) was purchased and dissolved in dimethyl sulfoxide.

Techniques: Transfection, Inhibition