h-nmr Search Results


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  • 95
    Millipore h nmr
    H Nmr, supplied by Millipore, used in various techniques. Bioz Stars score: 95/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Bruker Corporation h nmr
    H Nmr, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 94/100, based on 2944 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    BOC Sciences h nmr spectra
    H Nmr Spectra, supplied by BOC Sciences, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Bruker Corporation h nmr spectra
    1 <t>H-NMR</t> of the separated pyridine onium salt; the signal at 2.51 ppm is attributed to <t>DMSO</t> solvent residue, and that at 3.35 ppm is attributed to water existed in DMSO- d 6 .
    H Nmr Spectra, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 94/100, based on 6241 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    JEOL h nmr system
    ( a ) 1 <t>H-NMR</t> spectra of PC 4 nanoassembly measured in D 2 O at pH 7.4, pH 6.5, and pH 5.5, respectively. ( b ) Relative peak intensity of curcumin in the nanoassembly measured in D 2 O at pH 5.5, pH 6.5, and pH 7.4, respectively. ( c ) pH-sensitive membrane-lytic activity of <t>CCM</t> nanoassemblies after 2 h of incubation with seep erythrocyte at pH 5.5, pH 6.5, and pH 7.4, respectively. Values are average of three separate experiments in triplicate and are expressed as mean ± SD.
    H Nmr System, supplied by JEOL, used in various techniques. Bioz Stars score: 85/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Millipore q1 h nmr
    ( a ) 1 <t>H-NMR</t> spectra of PC 4 nanoassembly measured in D 2 O at pH 7.4, pH 6.5, and pH 5.5, respectively. ( b ) Relative peak intensity of curcumin in the nanoassembly measured in D 2 O at pH 5.5, pH 6.5, and pH 7.4, respectively. ( c ) pH-sensitive membrane-lytic activity of <t>CCM</t> nanoassemblies after 2 h of incubation with seep erythrocyte at pH 5.5, pH 6.5, and pH 7.4, respectively. Values are average of three separate experiments in triplicate and are expressed as mean ± SD.
    Q1 H Nmr, supplied by Millipore, used in various techniques. Bioz Stars score: 92/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Bruker Corporation h nmr spectrometer
    1 <t>H-NMR</t> spectra of: ( A ) free <t>PPD;</t> ( B ) phospholipids; ( C ) PPD-PLC; and ( D ) physical mixture of PPD and phospholipids.
    H Nmr Spectrometer, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 91/100, based on 28 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/h nmr spectrometer/product/Bruker Corporation
    Average 91 stars, based on 28 article reviews
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    90
    Millipore h nmr spectrum
    1 <t>H-NMR</t> spectra of: ( A ) free <t>PPD;</t> ( B ) phospholipids; ( C ) PPD-PLC; and ( D ) physical mixture of PPD and phospholipids.
    H Nmr Spectrum, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Agilent technologies h nmr spectrometer
    1 <t>H-NMR</t> spectra of: ( A ) free <t>PPD;</t> ( B ) phospholipids; ( C ) PPD-PLC; and ( D ) physical mixture of PPD and phospholipids.
    H Nmr Spectrometer, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 91/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Bruker Corporation h nmr spectroscopy
    1 H <t>NMR</t> spectra in CD 3 OD of Rhodamine B isothiocyanate (bottom left), PAMAM dendrimer (G = 5) (middle left), Rhodamine-PAMAM <t>(Rho-PAM)</t> bioconjugate (upper left). On the right, a magnification of the aromatic protons of the derivatives: Rho 1% -PAM (bottom right), Rho 25% -PAM (middle right), Rho 50% -PAM (upper right). All proton resonances were assigned according to the scheme depicted in the upper part of the picture.
    H Nmr Spectroscopy, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 91/100, based on 584 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 91 stars, based on 584 article reviews
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    98
    Bruker Corporation h nmr analyzer
    1 H <t>NMR</t> spectra in CD 3 OD of Rhodamine B isothiocyanate (bottom left), PAMAM dendrimer (G = 5) (middle left), Rhodamine-PAMAM <t>(Rho-PAM)</t> bioconjugate (upper left). On the right, a magnification of the aromatic protons of the derivatives: Rho 1% -PAM (bottom right), Rho 25% -PAM (middle right), Rho 50% -PAM (upper right). All proton resonances were assigned according to the scheme depicted in the upper part of the picture.
    H Nmr Analyzer, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 98/100, based on 56 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    Bruker Corporation av 500 hydrogen nuclear magnetic resonance spectrometer
    1 H <t>NMR</t> spectra in CD 3 OD of Rhodamine B isothiocyanate (bottom left), PAMAM dendrimer (G = 5) (middle left), Rhodamine-PAMAM <t>(Rho-PAM)</t> bioconjugate (upper left). On the right, a magnification of the aromatic protons of the derivatives: Rho 1% -PAM (bottom right), Rho 25% -PAM (middle right), Rho 50% -PAM (upper right). All proton resonances were assigned according to the scheme depicted in the upper part of the picture.
    Av 500 Hydrogen Nuclear Magnetic Resonance Spectrometer, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 93/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Agilent technologies h nmr spectroscopy
    <t>DBC</t> and chitin characterization. Solid state 13 <t>C-NMR</t> of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).
    H Nmr Spectroscopy, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 91/100, based on 31 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Liposcience h nmr spectroscopy
    <t>DBC</t> and chitin characterization. Solid state 13 <t>C-NMR</t> of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).
    H Nmr Spectroscopy, supplied by Liposcience, used in various techniques. Bioz Stars score: 91/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    JEOL h nmr spectroscopy
    <t>DBC</t> and chitin characterization. Solid state 13 <t>C-NMR</t> of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).
    H Nmr Spectroscopy, supplied by JEOL, used in various techniques. Bioz Stars score: 90/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Bruker Corporation h nmr spectrometry
    <t>DBC</t> and chitin characterization. Solid state 13 <t>C-NMR</t> of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).
    H Nmr Spectrometry, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 85/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Agilent technologies h nmr
    <t>DBC</t> and chitin characterization. Solid state 13 <t>C-NMR</t> of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).
    H Nmr, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 92/100, based on 132 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    Varian Medical hydrogen nuclear magnetic resonance
    <t>DBC</t> and chitin characterization. Solid state 13 <t>C-NMR</t> of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).
    Hydrogen Nuclear Magnetic Resonance, supplied by Varian Medical, used in various techniques. Bioz Stars score: 88/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    1 H-NMR of the separated pyridine onium salt; the signal at 2.51 ppm is attributed to DMSO solvent residue, and that at 3.35 ppm is attributed to water existed in DMSO- d 6 .

    Journal: Molecules

    Article Title: 4-N,N-Dimethylaminopyridine Promoted Selective Oxidation of Methyl Aromatics with Molecular Oxygen

    doi: 10.3390/molecules17043957

    Figure Lengend Snippet: 1 H-NMR of the separated pyridine onium salt; the signal at 2.51 ppm is attributed to DMSO solvent residue, and that at 3.35 ppm is attributed to water existed in DMSO- d 6 .

    Article Snippet: The 1 H-NMR spectra were recorded in DMSO-d 6 on a Bruker 400 MHz NMR spectrometer with TMS as internal standard.

    Techniques: Nuclear Magnetic Resonance

    ( a ) 1 H-NMR spectra of PC 4 nanoassembly measured in D 2 O at pH 7.4, pH 6.5, and pH 5.5, respectively. ( b ) Relative peak intensity of curcumin in the nanoassembly measured in D 2 O at pH 5.5, pH 6.5, and pH 7.4, respectively. ( c ) pH-sensitive membrane-lytic activity of CCM nanoassemblies after 2 h of incubation with seep erythrocyte at pH 5.5, pH 6.5, and pH 7.4, respectively. Values are average of three separate experiments in triplicate and are expressed as mean ± SD.

    Journal: Scientific Reports

    Article Title: Discovery of a new function of curcumin which enhances its anticancer therapeutic potency

    doi: 10.1038/srep30962

    Figure Lengend Snippet: ( a ) 1 H-NMR spectra of PC 4 nanoassembly measured in D 2 O at pH 7.4, pH 6.5, and pH 5.5, respectively. ( b ) Relative peak intensity of curcumin in the nanoassembly measured in D 2 O at pH 5.5, pH 6.5, and pH 7.4, respectively. ( c ) pH-sensitive membrane-lytic activity of CCM nanoassemblies after 2 h of incubation with seep erythrocyte at pH 5.5, pH 6.5, and pH 7.4, respectively. Values are average of three separate experiments in triplicate and are expressed as mean ± SD.

    Article Snippet: Characterization of the obtained CCM amphiphiles were carried out by 1 H-NMR measurement (JEOL, ECA-500, solvent: CDCl3 ) and gel permeation chromatography (GPC) (JASCO, HPLC LC-2000Plus, column: TSKgel® , detector: RI, standard: PEG, eluent: DMSO dissolving 10 mM LiBr).

    Techniques: Nuclear Magnetic Resonance, Activity Assay, Incubation

    1 H-NMR spectra of: ( A ) free PPD; ( B ) phospholipids; ( C ) PPD-PLC; and ( D ) physical mixture of PPD and phospholipids.

    Journal: Molecules

    Article Title: 20(S)-Protopanaxadiol Phospholipid Complex: Process Optimization, Characterization, In Vitro Dissolution and Molecular Docking Studies

    doi: 10.3390/molecules21101396

    Figure Lengend Snippet: 1 H-NMR spectra of: ( A ) free PPD; ( B ) phospholipids; ( C ) PPD-PLC; and ( D ) physical mixture of PPD and phospholipids.

    Article Snippet: 1 H-NMR The samples (free PPD, phospholipids, physical mixture and PPD-PLC) were dissolved in deuterium-substituted solvent and analyzed using a 1 H-NMR spectrometer (AVANCE III UltraShield-Plus NMR Spectrometer, Bruker, Switzerland) at 400 MHz.

    Techniques: Nuclear Magnetic Resonance, Planar Chromatography

    1 H NMR spectra in CD 3 OD of Rhodamine B isothiocyanate (bottom left), PAMAM dendrimer (G = 5) (middle left), Rhodamine-PAMAM (Rho-PAM) bioconjugate (upper left). On the right, a magnification of the aromatic protons of the derivatives: Rho 1% -PAM (bottom right), Rho 25% -PAM (middle right), Rho 50% -PAM (upper right). All proton resonances were assigned according to the scheme depicted in the upper part of the picture.

    Journal: Scientific Reports

    Article Title: MicroRNAs delivery into human cells grown on 3D-printed PLA scaffolds coated with a novel fluorescent PAMAM dendrimer for biomedical applications

    doi: 10.1038/s41598-018-32258-9

    Figure Lengend Snippet: 1 H NMR spectra in CD 3 OD of Rhodamine B isothiocyanate (bottom left), PAMAM dendrimer (G = 5) (middle left), Rhodamine-PAMAM (Rho-PAM) bioconjugate (upper left). On the right, a magnification of the aromatic protons of the derivatives: Rho 1% -PAM (bottom right), Rho 25% -PAM (middle right), Rho 50% -PAM (upper right). All proton resonances were assigned according to the scheme depicted in the upper part of the picture.

    Article Snippet: The characterization of Rho-PAM compounds was carried out by 1 H-NMR spectroscopy in CD3 OD and recorded on a Bruker AC300P spectrometer.

    Techniques: Nuclear Magnetic Resonance

    DBC and chitin characterization. Solid state 13 C-NMR of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).

    Journal: Acta biomaterialia

    Article Title: Fabrication of magnetic and fluorescent chitin and dibutyrylchitin sub-micron particles by oil-in-water emulsification

    doi: 10.1016/j.actbio.2016.08.057

    Figure Lengend Snippet: DBC and chitin characterization. Solid state 13 C-NMR of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).

    Article Snippet: 1 H-NMR spectroscopy (500 MHz, Agilent DirectDrive 2) of DBC in chloroform-d and FTIR spectroscopy (Galaxy Series FTIR 3000, Mattson, USA) of chitin and DBC in KBr tablets were performed to analyze the functionalization of the chitin.

    Techniques: Nuclear Magnetic Resonance