sequant zic philic column  (Millipore)

 
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    Name:
    Ultraviolet visible near infrared wavelength wavenumber transmission standard
    Description:
    SRM 2035A cert SRM 2035A SDS
    Catalog Number:
    NIST2035A
    Price:
    None
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    Structured Review

    Millipore sequant zic philic column
    SRM 2035A cert SRM 2035A SDS
    https://www.bioz.com/result/sequant zic philic column/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    sequant zic philic column - by Bioz Stars, 2021-06
    86/100 stars

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    Related Articles

    Spectroscopy:

    Article Title: The Binding Effect of Proteins on Medications and Its Impact on Electrochemical Sensing: Antipsychotic Clozapine as a Case Study
    Article Snippet: .. Ultraviolet Visible Spectroscopy Each sample (50 μL) was transferred to a UV-transparent 96-well Microtiter plate (Sigma), both before filtration and from the resulting filtrate, and absorbance spectra recorded using a SpectraMax Plus 384 (Molecular Devices, Sunnyvale, CA, USA). .. Analysis to control for nonspecific membrane binding (NSMB) of free CLZ to the filter membrane was performed by comparing the filtrate absorbance to that of the unfiltered solution at 205 nm wavelength.

    Article Title: Biosynthesis, characterization, and evaluation of bioactivities of leaf extract-mediated biocompatible silver nanoparticles from an early tracheophyte, Pteris tripartita Sw.
    Article Snippet: .. Ultraviolet-visible spectroscopy and Fourier transform infrared spectroscopy analysis Silver nitrate (AgNO3 ) was purchased from Sigma-Aldrich Co. (St Louis, MO, USA) and a 1 M solution of AgNO3 was prepared. ..

    Filtration:

    Article Title: The Binding Effect of Proteins on Medications and Its Impact on Electrochemical Sensing: Antipsychotic Clozapine as a Case Study
    Article Snippet: .. Ultraviolet Visible Spectroscopy Each sample (50 μL) was transferred to a UV-transparent 96-well Microtiter plate (Sigma), both before filtration and from the resulting filtrate, and absorbance spectra recorded using a SpectraMax Plus 384 (Molecular Devices, Sunnyvale, CA, USA). .. Analysis to control for nonspecific membrane binding (NSMB) of free CLZ to the filter membrane was performed by comparing the filtrate absorbance to that of the unfiltered solution at 205 nm wavelength.

    Concentration Assay:

    Article Title: Evaluation of the Rheologic and Physicochemical Properties of a Novel Hyaluronic Acid Filler Range with eXcellent Three-Dimensional Reticulation (XTR™) Technology
    Article Snippet: It is used also to assess the ability of fillers to resist vertical compression/stretching and is the expression of the strength of internal forces that can be modified based on the HA concentration, the crosslinking technology and the different gel macrostructures (biphasic or monophasic gel) [ , ]. .. Calibration curves (absorbance vs concentration) were calculated from the spectra from visible light to ultraviolet wavelength for each compound. .. Calibration curves (absorbance vs concentration) were calculated from the spectra from visible light to ultraviolet wavelength for each compound.

    Article Title: Phosphatidylserine Asymmetry Promotes the Membrane Insertion of a Transmembrane Helix
    Article Snippet: Annexin V, Alexa Fluor 568 conjugate (Annexin V-568), was purchased form Thermo Fisher Scientific (Waltham, MA) and assayed for concentration with an Agilent Cary 100 Ultraviolet-Visible Spectrophotometer (Agilent Technologies, Santa Clara, CA) using an extinction coefficient of 23,380 M−1 cm−1 . pHLIP (sequence: Nt -AAEQNPIYWARYADWLFTTPLLLLDLALLVDADEGTCG-Ct ), synthesized using standard solid phase protocols and purified by reverse-phase high performance liquid chromatography to greater than 95% purity, was purchased from P3 BioSystems (Louisville, KY). .. A lyophilized pHLIP stock was dissolved in buffer (10 mM NaPi (pH 8.0)) and assayed for concentration by ultraviolet-visible using an extinction coefficient of 13,940 M−1 cm−1 . .. Methyl- β -cyclodextrin (m β CD), sucrose, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid) (HEPES), 2-( N -morpholino) ethanesulfonic acid (MES), calcium chloride (CaCl2), sodium acetate (NaOAc) buffer, and sodium phosphate (NaPi) buffer were all purchased from Sigma-Aldrich (St. Louis, MO).

    Polymerase Chain Reaction:

    Article Title: Guanidino-Acetic Acid: A Scarce Substance in Biomass That Can Regulate Postmortem Meat Glycolysis of Broilers Subjected to Pre-slaughter Transportation
    Article Snippet: A 10-μL volume of each sample was injected into an Alliance HPLC system (Alliance HPLC system 2695, Water Corporation, Milford, MA, United States) equipped with a Waters SunFire C18 column (250 mm × 4.6 mm, 5 μm) at a temperature of 25°C for Cr and PCr determination, and at a temperature of 30°C for ATP, ADP, and AMP analysis. .. The ultraviolet wavelength for Cr and PCr determination and the analysis of ATP, ADP, and AMP were 210 and 245 nm, respectively. .. The mobile phase was a mixture of methyl cyanides and 29.4 mM KH2 PO4 buffer (2:98, volume ratio) for Cr and PCr determination and was a mixture of methanol and phosphate buffer (13.5:86.5, volume ratio) for ATP, ADP, and AMP analysis, and the flow rate was 1 mL/min.

    MTT Assay:

    Article Title: Anticancer Activity of Methanol Extract of Ficus carica Leaves and Fruits Against Proliferation, Apoptosis, and Necrosis in Huh7it Cells
    Article Snippet: .. The other materials used were absolute Methanol (Sigma-Aldrich, St. Louis, MO, USA), ultraviolet-visible (UV-vis) spectrophotometers, Quvetes Glass, 2,2-diphenyl-1-picrylhydrazyl (DPPH), MTT (3-(4,5-dimethylthiazol-2yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) solution (Sigma-Aldrich, St. Louis, MO, USA), dimethyl sulfoxide (DMSO), GloMax-Multi Microplate Multimode Reader (Promega Corp., WI, USA), Huh7it cell line, phosphate-buffered saline (PBS), Annexin-PI, BD Biosciences FACS CaliburTM flow cytometry, DMEM (Gibco BRL, Grand Island, NY, USA), t-EDTA, Dulbecco PBS (D-PBS, Gibco BRL, Grand Island, NY, USA), nonessential amino acid, fetal bovine serum (FBS, Gibco BRL, Grand Island, NY, USA), Dulbecco’s modified Eagle’s Medium (Invitrogen, Carlsbad, CA, USA), kanamycin (Sigma-Aldrich, St. Louis, MO, USA), and nonessential amino acids (Invitrogen). ..

    FACS:

    Article Title: Anticancer Activity of Methanol Extract of Ficus carica Leaves and Fruits Against Proliferation, Apoptosis, and Necrosis in Huh7it Cells
    Article Snippet: .. The other materials used were absolute Methanol (Sigma-Aldrich, St. Louis, MO, USA), ultraviolet-visible (UV-vis) spectrophotometers, Quvetes Glass, 2,2-diphenyl-1-picrylhydrazyl (DPPH), MTT (3-(4,5-dimethylthiazol-2yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) solution (Sigma-Aldrich, St. Louis, MO, USA), dimethyl sulfoxide (DMSO), GloMax-Multi Microplate Multimode Reader (Promega Corp., WI, USA), Huh7it cell line, phosphate-buffered saline (PBS), Annexin-PI, BD Biosciences FACS CaliburTM flow cytometry, DMEM (Gibco BRL, Grand Island, NY, USA), t-EDTA, Dulbecco PBS (D-PBS, Gibco BRL, Grand Island, NY, USA), nonessential amino acid, fetal bovine serum (FBS, Gibco BRL, Grand Island, NY, USA), Dulbecco’s modified Eagle’s Medium (Invitrogen, Carlsbad, CA, USA), kanamycin (Sigma-Aldrich, St. Louis, MO, USA), and nonessential amino acids (Invitrogen). ..

    Flow Cytometry:

    Article Title: Anticancer Activity of Methanol Extract of Ficus carica Leaves and Fruits Against Proliferation, Apoptosis, and Necrosis in Huh7it Cells
    Article Snippet: .. The other materials used were absolute Methanol (Sigma-Aldrich, St. Louis, MO, USA), ultraviolet-visible (UV-vis) spectrophotometers, Quvetes Glass, 2,2-diphenyl-1-picrylhydrazyl (DPPH), MTT (3-(4,5-dimethylthiazol-2yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) solution (Sigma-Aldrich, St. Louis, MO, USA), dimethyl sulfoxide (DMSO), GloMax-Multi Microplate Multimode Reader (Promega Corp., WI, USA), Huh7it cell line, phosphate-buffered saline (PBS), Annexin-PI, BD Biosciences FACS CaliburTM flow cytometry, DMEM (Gibco BRL, Grand Island, NY, USA), t-EDTA, Dulbecco PBS (D-PBS, Gibco BRL, Grand Island, NY, USA), nonessential amino acid, fetal bovine serum (FBS, Gibco BRL, Grand Island, NY, USA), Dulbecco’s modified Eagle’s Medium (Invitrogen, Carlsbad, CA, USA), kanamycin (Sigma-Aldrich, St. Louis, MO, USA), and nonessential amino acids (Invitrogen). ..

    Cytometry:

    Article Title: Anticancer Activity of Methanol Extract of Ficus carica Leaves and Fruits Against Proliferation, Apoptosis, and Necrosis in Huh7it Cells
    Article Snippet: .. The other materials used were absolute Methanol (Sigma-Aldrich, St. Louis, MO, USA), ultraviolet-visible (UV-vis) spectrophotometers, Quvetes Glass, 2,2-diphenyl-1-picrylhydrazyl (DPPH), MTT (3-(4,5-dimethylthiazol-2yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) solution (Sigma-Aldrich, St. Louis, MO, USA), dimethyl sulfoxide (DMSO), GloMax-Multi Microplate Multimode Reader (Promega Corp., WI, USA), Huh7it cell line, phosphate-buffered saline (PBS), Annexin-PI, BD Biosciences FACS CaliburTM flow cytometry, DMEM (Gibco BRL, Grand Island, NY, USA), t-EDTA, Dulbecco PBS (D-PBS, Gibco BRL, Grand Island, NY, USA), nonessential amino acid, fetal bovine serum (FBS, Gibco BRL, Grand Island, NY, USA), Dulbecco’s modified Eagle’s Medium (Invitrogen, Carlsbad, CA, USA), kanamycin (Sigma-Aldrich, St. Louis, MO, USA), and nonessential amino acids (Invitrogen). ..

    Modification:

    Article Title: Anticancer Activity of Methanol Extract of Ficus carica Leaves and Fruits Against Proliferation, Apoptosis, and Necrosis in Huh7it Cells
    Article Snippet: .. The other materials used were absolute Methanol (Sigma-Aldrich, St. Louis, MO, USA), ultraviolet-visible (UV-vis) spectrophotometers, Quvetes Glass, 2,2-diphenyl-1-picrylhydrazyl (DPPH), MTT (3-(4,5-dimethylthiazol-2yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) solution (Sigma-Aldrich, St. Louis, MO, USA), dimethyl sulfoxide (DMSO), GloMax-Multi Microplate Multimode Reader (Promega Corp., WI, USA), Huh7it cell line, phosphate-buffered saline (PBS), Annexin-PI, BD Biosciences FACS CaliburTM flow cytometry, DMEM (Gibco BRL, Grand Island, NY, USA), t-EDTA, Dulbecco PBS (D-PBS, Gibco BRL, Grand Island, NY, USA), nonessential amino acid, fetal bovine serum (FBS, Gibco BRL, Grand Island, NY, USA), Dulbecco’s modified Eagle’s Medium (Invitrogen, Carlsbad, CA, USA), kanamycin (Sigma-Aldrich, St. Louis, MO, USA), and nonessential amino acids (Invitrogen). ..

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  • 86
    Millipore well recognized sequant zic philic columns
    Application of the redox metabolite detection method for mammalian tissues; ( a , b ) Top 25 differentially detected metabolites between three chromatographic methods in mouse liver ( a ) and kidney ( b ) presented in a heatmap for each organ. Each replicate is a tissue chunk from an independent mouse, extracted in buffer C+Ell and then split in three and run on the different chromatographies. <t>ZIC:</t> <t>ZIC-pHILIC,</t> Acc: Accucore-NH2, LUNA: LUNA-NH2; ( c ) Venn diagram of total detected metabolites in liver and kidney between the three chromatographic methods from ( a , b ) and the overlap between them. Only metabolites passing 30% CV cutoff were compared; ( d ) Global PCA analysis of polar metabolites detection in mouse liver samples extracted by three different buffers (B, C, C plus Ellman’s) and detected by LC-MS using the ZIC-pHILIC column; Each replicate represents a liver chunk from an independent mouse, subdivided evenly between three tubes and extracted using the different buffers. This experiment was performed twice and a representative replicate is shown; ( e ) Top 25 differentially detected metabolites in mouse liver samples from ( d ); ( f ) Detection of redox metabolites from mouse liver, kidney, CSF, and plasma extracted in three different buffers (B, C, and C plus Ellman’s). These experiments were performed twice (except for plasma) and a representative replicate is shown. Each dot represents a measurement from an independent mouse, mean and standard deviation are indicated; statistical significance was determined using Anova with correction for multiple comparisons by false discovery rate correction. Only significant q-values are indicated (except for GSH and GSH-Ell levels, which were excluded from analysis).
    Well Recognized Sequant Zic Philic Columns, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/well recognized sequant zic philic columns/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    well recognized sequant zic philic columns - by Bioz Stars, 2021-06
    86/100 stars
      Buy from Supplier

    94
    Millipore sequant zic philic column
    Application of the redox metabolite detection method for mammalian tissues; ( a , b ) Top 25 differentially detected metabolites between three chromatographic methods in mouse liver ( a ) and kidney ( b ) presented in a heatmap for each organ. Each replicate is a tissue chunk from an independent mouse, extracted in buffer C+Ell and then split in three and run on the different chromatographies. <t>ZIC:</t> <t>ZIC-pHILIC,</t> Acc: Accucore-NH2, LUNA: LUNA-NH2; ( c ) Venn diagram of total detected metabolites in liver and kidney between the three chromatographic methods from ( a , b ) and the overlap between them. Only metabolites passing 30% CV cutoff were compared; ( d ) Global PCA analysis of polar metabolites detection in mouse liver samples extracted by three different buffers (B, C, C plus Ellman’s) and detected by LC-MS using the ZIC-pHILIC column; Each replicate represents a liver chunk from an independent mouse, subdivided evenly between three tubes and extracted using the different buffers. This experiment was performed twice and a representative replicate is shown; ( e ) Top 25 differentially detected metabolites in mouse liver samples from ( d ); ( f ) Detection of redox metabolites from mouse liver, kidney, CSF, and plasma extracted in three different buffers (B, C, and C plus Ellman’s). These experiments were performed twice (except for plasma) and a representative replicate is shown. Each dot represents a measurement from an independent mouse, mean and standard deviation are indicated; statistical significance was determined using Anova with correction for multiple comparisons by false discovery rate correction. Only significant q-values are indicated (except for GSH and GSH-Ell levels, which were excluded from analysis).
    Sequant Zic Philic Column, supplied by Millipore, 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/result/sequant zic philic column/product/Millipore
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    sequant zic philic column - by Bioz Stars, 2021-06
    94/100 stars
      Buy from Supplier

    80
    Millipore sequant zic philic polymeric column
    Application of the redox metabolite detection method for mammalian tissues; ( a , b ) Top 25 differentially detected metabolites between three chromatographic methods in mouse liver ( a ) and kidney ( b ) presented in a heatmap for each organ. Each replicate is a tissue chunk from an independent mouse, extracted in buffer C+Ell and then split in three and run on the different chromatographies. <t>ZIC:</t> <t>ZIC-pHILIC,</t> Acc: Accucore-NH2, LUNA: LUNA-NH2; ( c ) Venn diagram of total detected metabolites in liver and kidney between the three chromatographic methods from ( a , b ) and the overlap between them. Only metabolites passing 30% CV cutoff were compared; ( d ) Global PCA analysis of polar metabolites detection in mouse liver samples extracted by three different buffers (B, C, C plus Ellman’s) and detected by LC-MS using the ZIC-pHILIC column; Each replicate represents a liver chunk from an independent mouse, subdivided evenly between three tubes and extracted using the different buffers. This experiment was performed twice and a representative replicate is shown; ( e ) Top 25 differentially detected metabolites in mouse liver samples from ( d ); ( f ) Detection of redox metabolites from mouse liver, kidney, CSF, and plasma extracted in three different buffers (B, C, and C plus Ellman’s). These experiments were performed twice (except for plasma) and a representative replicate is shown. Each dot represents a measurement from an independent mouse, mean and standard deviation are indicated; statistical significance was determined using Anova with correction for multiple comparisons by false discovery rate correction. Only significant q-values are indicated (except for GSH and GSH-Ell levels, which were excluded from analysis).
    Sequant Zic Philic Polymeric Column, supplied by Millipore, used in various techniques. Bioz Stars score: 80/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sequant zic philic polymeric column/product/Millipore
    Average 80 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    sequant zic philic polymeric column - by Bioz Stars, 2021-06
    80/100 stars
      Buy from Supplier

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    Application of the redox metabolite detection method for mammalian tissues; ( a , b ) Top 25 differentially detected metabolites between three chromatographic methods in mouse liver ( a ) and kidney ( b ) presented in a heatmap for each organ. Each replicate is a tissue chunk from an independent mouse, extracted in buffer C+Ell and then split in three and run on the different chromatographies. ZIC: ZIC-pHILIC, Acc: Accucore-NH2, LUNA: LUNA-NH2; ( c ) Venn diagram of total detected metabolites in liver and kidney between the three chromatographic methods from ( a , b ) and the overlap between them. Only metabolites passing 30% CV cutoff were compared; ( d ) Global PCA analysis of polar metabolites detection in mouse liver samples extracted by three different buffers (B, C, C plus Ellman’s) and detected by LC-MS using the ZIC-pHILIC column; Each replicate represents a liver chunk from an independent mouse, subdivided evenly between three tubes and extracted using the different buffers. This experiment was performed twice and a representative replicate is shown; ( e ) Top 25 differentially detected metabolites in mouse liver samples from ( d ); ( f ) Detection of redox metabolites from mouse liver, kidney, CSF, and plasma extracted in three different buffers (B, C, and C plus Ellman’s). These experiments were performed twice (except for plasma) and a representative replicate is shown. Each dot represents a measurement from an independent mouse, mean and standard deviation are indicated; statistical significance was determined using Anova with correction for multiple comparisons by false discovery rate correction. Only significant q-values are indicated (except for GSH and GSH-Ell levels, which were excluded from analysis).

    Journal: Metabolites

    Article Title: Redox Metabolism Measurement in Mammalian Cells and Tissues by LC-MS

    doi: 10.3390/metabo11050313

    Figure Lengend Snippet: Application of the redox metabolite detection method for mammalian tissues; ( a , b ) Top 25 differentially detected metabolites between three chromatographic methods in mouse liver ( a ) and kidney ( b ) presented in a heatmap for each organ. Each replicate is a tissue chunk from an independent mouse, extracted in buffer C+Ell and then split in three and run on the different chromatographies. ZIC: ZIC-pHILIC, Acc: Accucore-NH2, LUNA: LUNA-NH2; ( c ) Venn diagram of total detected metabolites in liver and kidney between the three chromatographic methods from ( a , b ) and the overlap between them. Only metabolites passing 30% CV cutoff were compared; ( d ) Global PCA analysis of polar metabolites detection in mouse liver samples extracted by three different buffers (B, C, C plus Ellman’s) and detected by LC-MS using the ZIC-pHILIC column; Each replicate represents a liver chunk from an independent mouse, subdivided evenly between three tubes and extracted using the different buffers. This experiment was performed twice and a representative replicate is shown; ( e ) Top 25 differentially detected metabolites in mouse liver samples from ( d ); ( f ) Detection of redox metabolites from mouse liver, kidney, CSF, and plasma extracted in three different buffers (B, C, and C plus Ellman’s). These experiments were performed twice (except for plasma) and a representative replicate is shown. Each dot represents a measurement from an independent mouse, mean and standard deviation are indicated; statistical significance was determined using Anova with correction for multiple comparisons by false discovery rate correction. Only significant q-values are indicated (except for GSH and GSH-Ell levels, which were excluded from analysis).

    Article Snippet: In addition to the well-recognized SeQuant ZIC-pHILIC columns (Millipore-Sigma, St. Louis, MI, USA) we decided to explore two more consistently available columns: Accucore-Amide HILIC (Thermo-Fisher Scientific, Waltham, MA, USA) and LUNA-NH2 (Phenomenex, Torrance, CA, USA).

    Techniques: Liquid Chromatography with Mass Spectroscopy, Standard Deviation

    A method to quantify redox metabolites by LC-MS; ( a,b ) Retention times and sensitivity comparison between three HILIC-based chromatography methods. Chromatographic runs were carried out on either ZIC-pHILIC (ZIC), Accucore-NH2 (ACC), or LUNA-NH2 (LUNA) with 20 min, 20 min, or 25 min linear gradients, respectively. Overlaid peaks are shown for the indicated range of ( a ) polar metabolite standards (see Table S1 for further details) and ( b ) GSH, GSH derivatized with Ellman’s (GSH-Ell), GSSG, NADH, and NADPH. Redox metabolites were diluted in 25 mM Ammonium Acetate and 2.5 mM Na-Ascorbate in water. Standards were dissolved in extraction buffer B (as detailed in Section 2.2 ); ( c ) Optimization of HESI parameters on orbitrap mass spectrometer for the indicated metabolites using ZIC-pHILIC chromatography and standards. Graphs represent integrated areas of chromatographic peaks under changing parameters for capillary temperature or S-lens; ( d ) Limit of detection and linearity for individual redox molecules. Presented are the average values and standard deviation.

    Journal: Metabolites

    Article Title: Redox Metabolism Measurement in Mammalian Cells and Tissues by LC-MS

    doi: 10.3390/metabo11050313

    Figure Lengend Snippet: A method to quantify redox metabolites by LC-MS; ( a,b ) Retention times and sensitivity comparison between three HILIC-based chromatography methods. Chromatographic runs were carried out on either ZIC-pHILIC (ZIC), Accucore-NH2 (ACC), or LUNA-NH2 (LUNA) with 20 min, 20 min, or 25 min linear gradients, respectively. Overlaid peaks are shown for the indicated range of ( a ) polar metabolite standards (see Table S1 for further details) and ( b ) GSH, GSH derivatized with Ellman’s (GSH-Ell), GSSG, NADH, and NADPH. Redox metabolites were diluted in 25 mM Ammonium Acetate and 2.5 mM Na-Ascorbate in water. Standards were dissolved in extraction buffer B (as detailed in Section 2.2 ); ( c ) Optimization of HESI parameters on orbitrap mass spectrometer for the indicated metabolites using ZIC-pHILIC chromatography and standards. Graphs represent integrated areas of chromatographic peaks under changing parameters for capillary temperature or S-lens; ( d ) Limit of detection and linearity for individual redox molecules. Presented are the average values and standard deviation.

    Article Snippet: In addition to the well-recognized SeQuant ZIC-pHILIC columns (Millipore-Sigma, St. Louis, MI, USA) we decided to explore two more consistently available columns: Accucore-Amide HILIC (Thermo-Fisher Scientific, Waltham, MA, USA) and LUNA-NH2 (Phenomenex, Torrance, CA, USA).

    Techniques: Liquid Chromatography with Mass Spectroscopy, Hydrophilic Interaction Liquid Chromatography, Chromatography, Mass Spectrometry, Standard Deviation