acetonitrile acn Millipore Search Results


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  • 99
    Millipore acetonitrile acn
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Acetonitrile Acn, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 1043 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore consumables acn
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Consumables Acn, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 205 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Millipore acetonitrile acn succinic d0 anhydride sigma
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Acetonitrile Acn Succinic D0 Anhydride Sigma, supplied by Millipore, used in various techniques. Bioz Stars score: 85/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore ergot alkaloids acetonitrile acn
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Ergot Alkaloids Acetonitrile Acn, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore acetonitrile acn trifluoroacetic acid
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Acetonitrile Acn Trifluoroacetic Acid, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore acn thf
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Acn Thf, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore liquid chromatography mass spectrometry lc ms grade acetonitrile acn
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Liquid Chromatography Mass Spectrometry Lc Ms Grade Acetonitrile Acn, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore high performance liquid chromatography acetonitrile acn
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    High Performance Liquid Chromatography Acetonitrile Acn, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    95
    Millipore acetonitrile water
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Acetonitrile Water, supplied by Millipore, used in various techniques. Bioz Stars score: 95/100, based on 175 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Merck KGaA acetonitrile
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Acetonitrile, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 99/100, based on 1122 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Millipore reference material irmm 316
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Reference Material Irmm 316, supplied by Millipore, used in various techniques. Bioz Stars score: 91/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore trifluoroacetic acid acn tfa
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Trifluoroacetic Acid Acn Tfa, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    87
    Millipore 100 0 1 v v acetonitrile
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    100 0 1 V V Acetonitrile, supplied by Millipore, used in various techniques. Bioz Stars score: 87/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    87
    Millipore reagents hplc grade acetonitrile
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Reagents Hplc Grade Acetonitrile, supplied by Millipore, used in various techniques. Bioz Stars score: 87/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    Millipore hplc
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Hplc, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 952 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore propargylamine
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Propargylamine, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 57 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore hplc grade solvents
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Hplc Grade Solvents, supplied by Millipore, used in various techniques. Bioz Stars score: 98/100, based on 488 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore hydroxytoluene
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Hydroxytoluene, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 726 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore protein elution buffer
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Protein Elution Buffer, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore buffer a
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Buffer A, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 10858 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    Millipore anhydrous
    Example of <t>PDA</t> reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 <t>ACN:PB</t> (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM
    Anhydrous, supplied by Millipore, used in various techniques. Bioz Stars score: 93/100, based on 106 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Example of PDA reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 ACN:PB (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM

    Journal: Toxicology

    Article Title: Pyridoxylamine reactivity kinetics as an amine based nucleophile for screening electrophilic dermal sensitizers

    doi: 10.1016/j.tox.2013.11.009

    Figure Lengend Snippet: Example of PDA reactivity. (i) Glutaraldehyde reactivity to 0.1 mM PDA was observed with (a) 1 mM, (b) 2 mM, (c) 4 mM, (d) 8 Mm and (e) 10 mM glutaraldehyde in 50:50 ACN:PB (pH 7.4). (ii) PDA (0.1 mM) was reacted with (a) 1, (b) 2, (c) 4, and (d) 8 mM

    Article Snippet: Phosphate buffer, acetonitrile (ACN), pyridoxylamine dihydrochloride (PDA; CAS # 524-36-7) and all test chemicals which were reagent grade were purchased from Sigma Chemical Co. (St. Louis, MO) and Fisher Scientific (Pittsburgh, PA) and used without further purification.

    Techniques:

    Kinetic changes during JBH treatment show that G 3 H 2 and G 3 H 3 species from SeHAS HA are sequentially converted to smaller members of the H 2 and H 3 series. Aliquots (5 µL) of Wash 3 were incubated with 22 µL inactive (time-zero) or active JBH at 30°C for up to 26 h ( n = 4 except n = 3 at 26 h); values are the mean intensity ± SEM as indicated. Members of the G 0–3 H 3 (A) and G 0–3 H 2 (B) series were analyzed to monitor decreases or increases in each member as a function of increasing JBH digestion time, (G 3 H 2,3 , ●; G 2 H 2,3 , ▼; G 1 H 2,3 , ▲; G 0 H 2,3 , ■). Lines ( r 2 ≥ 0.97) for H 2,3 (solid) and G 3 H 2,3 (long dash) were calculated by linear regression or a 3-parameter hyperbolic decay function, respectively, using Sigma Plot v10. Lines for G 2 H 2,3 (short dash) and G 1 H 2,3 (dotted) are comprised of linear segments. (C) ACN fraction samples (10 μL) containing G 4 H 2 and much less or no smaller members of this G n H 2 series were incubated for up to 12 h, as indicated, with 22 µL of inactive (time-zero) or active JBH. Sequential and time-dependent changes in the levels of G 3 H 2 , G 2 H 2 , G 1 H 2 and H 2 are evident.

    Journal: Glycobiology

    Article Title: Hyaluronan synthase assembles hyaluronan on a [GlcNAc(β1,4)]n-GlcNAc(α1→)UDP primer and hyaluronan retains this residual chitin oligomer as a cap at the nonreducing end

    doi: 10.1093/glycob/cwx012

    Figure Lengend Snippet: Kinetic changes during JBH treatment show that G 3 H 2 and G 3 H 3 species from SeHAS HA are sequentially converted to smaller members of the H 2 and H 3 series. Aliquots (5 µL) of Wash 3 were incubated with 22 µL inactive (time-zero) or active JBH at 30°C for up to 26 h ( n = 4 except n = 3 at 26 h); values are the mean intensity ± SEM as indicated. Members of the G 0–3 H 3 (A) and G 0–3 H 2 (B) series were analyzed to monitor decreases or increases in each member as a function of increasing JBH digestion time, (G 3 H 2,3 , ●; G 2 H 2,3 , ▼; G 1 H 2,3 , ▲; G 0 H 2,3 , ■). Lines ( r 2 ≥ 0.97) for H 2,3 (solid) and G 3 H 2,3 (long dash) were calculated by linear regression or a 3-parameter hyperbolic decay function, respectively, using Sigma Plot v10. Lines for G 2 H 2,3 (short dash) and G 1 H 2,3 (dotted) are comprised of linear segments. (C) ACN fraction samples (10 μL) containing G 4 H 2 and much less or no smaller members of this G n H 2 series were incubated for up to 12 h, as indicated, with 22 µL of inactive (time-zero) or active JBH. Sequential and time-dependent changes in the levels of G 3 H 2 , G 2 H 2 , G 1 H 2 and H 2 are evident.

    Article Snippet: Jack bean β-N-acetylhexosaminidase (JBH, #A2264), Streptomyces hyalurolyticus hyaluronidase (HA lyase, #H1136), OTH (#H-6254), and ACN (HPLC grade) were from Sigma-Aldrich (St. Louis, MO).

    Techniques: Incubation

    JBH digestion of G n H n species from SeHAS HA releases nondehydro NR-end H 2 and H 3 oligos. A–F. Selected m/z ranges are shown for Wash 3 (0.5 μL) samples treated overnight at 30°C with inactive (A, C, E) or active (B, D, F) JBH and analyzed by MALDI-TOF MS in negative mode. G n H n species that decrease or increase, with active JBH treatment, are indicated in italic or boldface font, respectively. New m/z signals are evident corresponding to H 2 (B compared to A), H 3 (D compared to C) and H 4 (F compared to E). (G–J) ACN samples (1, 2 or 3 µL), as indicated, were incubated overnight at 30°C with active or inactive JBH, and the presence of m / z signals, proportionally increasing with sample volume, was monitored for H 2 (panel G) or H 3 (panel H). The m / z signal decreases for the larger G 4 H 3 (I) and G 4 H 2 (J) ions were assessed in the 3 µL samples, treated with active (top) or inactive (bottom) JBH.

    Journal: Glycobiology

    Article Title: Hyaluronan synthase assembles hyaluronan on a [GlcNAc(β1,4)]n-GlcNAc(α1→)UDP primer and hyaluronan retains this residual chitin oligomer as a cap at the nonreducing end

    doi: 10.1093/glycob/cwx012

    Figure Lengend Snippet: JBH digestion of G n H n species from SeHAS HA releases nondehydro NR-end H 2 and H 3 oligos. A–F. Selected m/z ranges are shown for Wash 3 (0.5 μL) samples treated overnight at 30°C with inactive (A, C, E) or active (B, D, F) JBH and analyzed by MALDI-TOF MS in negative mode. G n H n species that decrease or increase, with active JBH treatment, are indicated in italic or boldface font, respectively. New m/z signals are evident corresponding to H 2 (B compared to A), H 3 (D compared to C) and H 4 (F compared to E). (G–J) ACN samples (1, 2 or 3 µL), as indicated, were incubated overnight at 30°C with active or inactive JBH, and the presence of m / z signals, proportionally increasing with sample volume, was monitored for H 2 (panel G) or H 3 (panel H). The m / z signal decreases for the larger G 4 H 3 (I) and G 4 H 2 (J) ions were assessed in the 3 µL samples, treated with active (top) or inactive (bottom) JBH.

    Article Snippet: Jack bean β-N-acetylhexosaminidase (JBH, #A2264), Streptomyces hyalurolyticus hyaluronidase (HA lyase, #H1136), OTH (#H-6254), and ACN (HPLC grade) were from Sigma-Aldrich (St. Louis, MO).

    Techniques: Mass Spectrometry, Incubation

    HPLC chromatography profiles of susceptible MJ (a) and resistant SA tick strains (b). At higher concentrations of ACN (acetonitrile), multiple peaks eluted in susceptible strain MJ ((a), upper), while at low concentrations of ACN, peaks were observed in resistant strain SA ((b), upper). The oxidizing activity exhibited through L-DOPA oxidation is depicted below the chromatograms ((a) and (b), lower); the graph exhibits an increase of oxidative activity approximately at 10 min retention time in the susceptible MJ when compared to the resistant SA; additionally, the resistant strain SA exhibits several peaks of oxidative activity which are not present in the susceptible strain MJ during the 20 to 30 min retention time.

    Journal: BioMed Research International

    Article Title: Comparative Hemolymph Proteomic and Enzymatic Analyses of Two Strains of Rhipicephalus (Boophilus) microplus Ticks Resistant and Susceptible to Ixodicides

    doi: 10.1155/2018/9451547

    Figure Lengend Snippet: HPLC chromatography profiles of susceptible MJ (a) and resistant SA tick strains (b). At higher concentrations of ACN (acetonitrile), multiple peaks eluted in susceptible strain MJ ((a), upper), while at low concentrations of ACN, peaks were observed in resistant strain SA ((b), upper). The oxidizing activity exhibited through L-DOPA oxidation is depicted below the chromatograms ((a) and (b), lower); the graph exhibits an increase of oxidative activity approximately at 10 min retention time in the susceptible MJ when compared to the resistant SA; additionally, the resistant strain SA exhibits several peaks of oxidative activity which are not present in the susceptible strain MJ during the 20 to 30 min retention time.

    Article Snippet: HPLC Fractioning The samples were applied on a C-18 reverse phase HPLC column on an Agilent 1100 series HPLC apparatus and eluted with a 0 to 50 % acetonitrile gradient (ACN) (SIGMA) with 25 minutes of collection and then with 50 to 100% ACN gradient within 20 minutes of collection.

    Techniques: High Performance Liquid Chromatography, Chromatography, Activity Assay

    Transient spectra of thymine following excitation at 270 nm in air-saturated acetonitrile- d 3  from 30 – 2800 ps (solid line). The spectrum from  from 0 – 1 µs is shown for comparison (dashed line).

    Journal:

    Article Title: Time-resolved infrared spectroscopy of the lowest triplet state of thymine and thymidine

    doi: 10.1016/j.chemphys.2007.10.035

    Figure Lengend Snippet: Transient spectra of thymine following excitation at 270 nm in air-saturated acetonitrile- d 3 from 30 – 2800 ps (solid line). The spectrum from from 0 – 1 µs is shown for comparison (dashed line).

    Article Snippet: Thymine (99%), thymidine (99%), D2 O (99.9% atom), and acetonitrile- d 3 (CD3 CN, > 99.998% atom purity) were purchased from Sigma-Aldrich and used as received.

    Techniques:

    Transient kinetics of thymine following excitation with a femtosecond pump pulse at 270 nm in air-saturated acetonitrile- d 3  at 1602 cm −1  (solid circles) and 1628 cm −1  (open circles). Delay times after 30 ps are shown on a logarithmic scale.

    Journal:

    Article Title: Time-resolved infrared spectroscopy of the lowest triplet state of thymine and thymidine

    doi: 10.1016/j.chemphys.2007.10.035

    Figure Lengend Snippet: Transient kinetics of thymine following excitation with a femtosecond pump pulse at 270 nm in air-saturated acetonitrile- d 3 at 1602 cm −1 (solid circles) and 1628 cm −1 (open circles). Delay times after 30 ps are shown on a logarithmic scale.

    Article Snippet: Thymine (99%), thymidine (99%), D2 O (99.9% atom), and acetonitrile- d 3 (CD3 CN, > 99.998% atom purity) were purchased from Sigma-Aldrich and used as received.

    Techniques:

    TRIR spectrum of thymine in argon-purged acetonitrile- d 3  at a delay of 0 − 1 µs (solid curve). Also shown is the inverted and scaled steady-state IR absorption spectrum (dashed curve). The inset compares the TRIR spectra of thymine (solid)

    Journal:

    Article Title: Time-resolved infrared spectroscopy of the lowest triplet state of thymine and thymidine

    doi: 10.1016/j.chemphys.2007.10.035

    Figure Lengend Snippet: TRIR spectrum of thymine in argon-purged acetonitrile- d 3 at a delay of 0 − 1 µs (solid curve). Also shown is the inverted and scaled steady-state IR absorption spectrum (dashed curve). The inset compares the TRIR spectra of thymine (solid)

    Article Snippet: Thymine (99%), thymidine (99%), D2 O (99.9% atom), and acetonitrile- d 3 (CD3 CN, > 99.998% atom purity) were purchased from Sigma-Aldrich and used as received.

    Techniques:

    TRIR spectra of thymidine in argon-purged acetonitrile- d 3  at delays of, from top to bottom: 0 – 1 µs, 1 – 2 µs, 2 – 3 µs, and 3 – 4.5 µs. Also shown is the inverted and scaled steady state

    Journal:

    Article Title: Time-resolved infrared spectroscopy of the lowest triplet state of thymine and thymidine

    doi: 10.1016/j.chemphys.2007.10.035

    Figure Lengend Snippet: TRIR spectra of thymidine in argon-purged acetonitrile- d 3 at delays of, from top to bottom: 0 – 1 µs, 1 – 2 µs, 2 – 3 µs, and 3 – 4.5 µs. Also shown is the inverted and scaled steady state

    Article Snippet: Thymine (99%), thymidine (99%), D2 O (99.9% atom), and acetonitrile- d 3 (CD3 CN, > 99.998% atom purity) were purchased from Sigma-Aldrich and used as received.

    Techniques:

    TRIR spectra of thymine- d 2  in argon-purged acetonitrile- d 3  at delays of (from top to bottom): 0 – 1 µs, 1 – 2 µs, 2 – 3 µs, and 3 – 4.5 µs. Also shown is the inverted, scaled FTIR spectrum

    Journal:

    Article Title: Time-resolved infrared spectroscopy of the lowest triplet state of thymine and thymidine

    doi: 10.1016/j.chemphys.2007.10.035

    Figure Lengend Snippet: TRIR spectra of thymine- d 2 in argon-purged acetonitrile- d 3 at delays of (from top to bottom): 0 – 1 µs, 1 – 2 µs, 2 – 3 µs, and 3 – 4.5 µs. Also shown is the inverted, scaled FTIR spectrum

    Article Snippet: Thymine (99%), thymidine (99%), D2 O (99.9% atom), and acetonitrile- d 3 (CD3 CN, > 99.998% atom purity) were purchased from Sigma-Aldrich and used as received.

    Techniques: