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reverse phase highperformance liquid chromatography hplc  (JASCO Inc)


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    JASCO Inc reverse phase highperformance liquid chromatography hplc
    Reverse Phase Highperformance Liquid Chromatography Hplc, supplied by JASCO Inc, used in various techniques. Bioz Stars score: 99/100, based on 29267 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/reversed+phase+hplc/JASCO+HPLC/pm42604468-122-0-19
    Average 99 stars, based on 29267 article reviews
    reverse phase highperformance liquid chromatography hplc - by Bioz Stars, 2026-09
    99/100 stars

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    High Performance Liquid Chromatography:

    Article Title: Lemna gibba Clones Show Differences in Phenotypic Responses to the Light Environment
    Article Snippet: .. Carotenoid composition was analyzed in 20 μL of the same aliquots by means of reversed-phase HPLC (Jasco, Tokyo, Japan), according to Láposi et al. [ ] and Oláh et al. [ ]. ..

    Article Title: Creation of Metal-Complex-Integrated Tensegrity Triangle DNA Crystals
    Article Snippet: .. The reaction mixture was passed through a spin column, and the product was purified via reversed-phase HPLC (JASCO) using a linear gradient of 2–40% acetonitrile (25min) with 20 mM ammonium formate. ( ). .. The UV/vis spectra of the A(T NH2 ) and A(T bpy ) were obtained by NanoDrop One (ThermoFisher, Waltham, MA, USA) ( ).

    Article Title: Topological Switch-OFF and β‑Galactosidase-Triggered Switch-ON of Cyclic Antisense Oligonucleotides via CuAAC for Controlled RNA Cleavage
    Article Snippet: .. The purity of the ASOs was confirmed by analytical reversed-phase HPLC using a JASCO MD-4015 photodiode array detector, PU-408i pump, a CO-4060 column oven, an LC-NetII/ADC interface, and a Waters XBridge C18 column (5 μm, 4.6 × 150 mm). ..

    Article Title: Structure-function relationship within helical peptoids for Cu 2+ chelation in the context of Alzheimer's disease.
    Article Snippet: Peptoids (N-substituted glycine oligomers) represent an excellent platform for drug development, such as selective chelators for Cu2+ ions towards chelation therapy, due to their efficient synthesis, high stability and good bioavailability.. We previously showed that peptoids helicity is essential for selective Cu2+ binding and identified a unique peptoid hexamer, having 2,2′:6′,2′′-terpyridine, and 8-hydroxyquinoline as metal-binding sidechains facing the same side of the helix, which exhibits high selectivity to Cu2+ ions.. However, maintaining a stable helix required the incorporation of bulky chiral sidechains, resulting in a hydrophobic peptoid, insoluble in aqueous solutions, and limited in its use as a drug candidate.

    Article Title: Topological Switch-OFF and β-Galactosidase-Triggered Switch-ON of Cyclic Antisense Oligonucleotides via CuAAC for Controlled RNA Cleavage.
    Article Snippet: Prodrug-type antisense oligonucleotides (ASOs) offer spatiotemporal control of gene silencing via external stimuli or intracellular enzyme activation.. However, a robust dual switch-off mechanism for phosphorothioate (PS)-modified gapmer ASOs, particularly involving topological constraints, has been largely unexplored.. This study aimed to design and synthesize novel βgalactosidase-responsive cyclic ASOs that achieve controlled RNA cleavage through both inhibited Watson−Crick base pairing and topological constraints.

    Article Title: A cocktail of Cu 2+ - and Zn 2+ -peptoid-based chelators can stop ROS formation for Alzheimer's disease therapy
    Article Snippet: .. Peptoid oligomers were analyzed by reversed-phase HPLC (analytical C18 column, 5 μm, 100 Å, 2.0x50 mm) on a Jasco UV-2075 instrument at 214 nm. ..

    Article Title: Acclimatization response to a short-term heat wave during summer in lactating Brown Swiss and Holstein Friesian cows
    Article Snippet: The ROM were determined with a Diacron International srl kit ( ). .. Retinol, tocopherol, and β -carotene concentrations were analyzed by reversed-phase HPLC (LC-4000, Jasco Europe SRL, Cremella, Italy) ( ). ..

    Purification:

    Article Title: Creation of Metal-Complex-Integrated Tensegrity Triangle DNA Crystals
    Article Snippet: .. The reaction mixture was passed through a spin column, and the product was purified via reversed-phase HPLC (JASCO) using a linear gradient of 2–40% acetonitrile (25min) with 20 mM ammonium formate. ( ). .. The UV/vis spectra of the A(T NH2 ) and A(T bpy ) were obtained by NanoDrop One (ThermoFisher, Waltham, MA, USA) ( ).



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    JASCO Inc reverse phase high performance liquid chromatography hplc system
    Light‐triggered chemical fuel generation from photolytic fuel‐carrier molecules. (a) Design and photolytic mechanism of fuel‐carrier molecules, ONB‐HFIP, which undergo UV‐triggered photolysis to release HFIP fuel and reaction byproducts. (b) Color change of ONB‐HFIP in solution as a function of UV irradiation time. (c) Time‐resolved <t>HPLC</t> chromatograms and (d) UV‐vis absorption spectra of ONB‐HFIP in solution as a function of UV irradiation time. (e) Conversion degree of photolytic reaction, estimated from the changing ratio of HPLC peak areas and UV‐vis absorption intensities at 343 and 264 nm over time.
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    Image Search Results


    Light‐triggered chemical fuel generation from photolytic fuel‐carrier molecules. (a) Design and photolytic mechanism of fuel‐carrier molecules, ONB‐HFIP, which undergo UV‐triggered photolysis to release HFIP fuel and reaction byproducts. (b) Color change of ONB‐HFIP in solution as a function of UV irradiation time. (c) Time‐resolved HPLC chromatograms and (d) UV‐vis absorption spectra of ONB‐HFIP in solution as a function of UV irradiation time. (e) Conversion degree of photolytic reaction, estimated from the changing ratio of HPLC peak areas and UV‐vis absorption intensities at 343 and 264 nm over time.

    Journal: Advanced Materials (Deerfield Beach, Fla.)

    Article Title: Photochemical Fuel Carrier Molecules for Robotic Embodied Energy

    doi: 10.1002/adma.202520447

    Figure Lengend Snippet: Light‐triggered chemical fuel generation from photolytic fuel‐carrier molecules. (a) Design and photolytic mechanism of fuel‐carrier molecules, ONB‐HFIP, which undergo UV‐triggered photolysis to release HFIP fuel and reaction byproducts. (b) Color change of ONB‐HFIP in solution as a function of UV irradiation time. (c) Time‐resolved HPLC chromatograms and (d) UV‐vis absorption spectra of ONB‐HFIP in solution as a function of UV irradiation time. (e) Conversion degree of photolytic reaction, estimated from the changing ratio of HPLC peak areas and UV‐vis absorption intensities at 343 and 264 nm over time.

    Article Snippet: High‐performance liquid chromatography (HPLC) spectra were obtained using an analytical reversed‐phase HPLC (Hitachi 5000 series Chromaster).

    Techniques: Irradiation