1 phenylethanol  (Millipore)


Bioz Verified Symbol Millipore is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 94
    Name:
    S 1 Phenylethanol
    Description:
    S 1 Phenylethanol also known as Methyl phenyl carbinol is formed from reduction of acetophenone
    Catalog Number:
    77849
    Price:
    None
    Buy from Supplier


    Structured Review

    Millipore 1 phenylethanol
    S 1 Phenylethanol
    S 1 Phenylethanol also known as Methyl phenyl carbinol is formed from reduction of acetophenone
    https://www.bioz.com/result/1 phenylethanol/product/Millipore
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    1 phenylethanol - by Bioz Stars, 2020-11
    94/100 stars

    Images

    1) Product Images from "Nanocellulose Derivative/Silica Hybrid Core-Shell Chiral Stationary Phase: Preparation and Enantioseparation Performance"

    Article Title: Nanocellulose Derivative/Silica Hybrid Core-Shell Chiral Stationary Phase: Preparation and Enantioseparation Performance

    Journal: Molecules

    doi: 10.3390/molecules21050561

    Chiral separation chromatograms of racemates on CPM2 column under normal phase mode. ( 1 ) 1-(1-naphthyl) ethanol; ( 2 ) benzoin methyl ether; ( 3 ) diclofop; ( 4 ) ranolazine; ( 5 ) metalaxyl; ( 6 ) 1-phenylethanol. Chromatographic conditions: mobile phase; ( 1 – 3 ) hexane/IPA (99.5/0.5, v / v ); ( 4 ) hexane/IPA (97/3, v / v ); ( 5 ) hexane/ethanol (97/3, v / v ); ( 6 ) hexane/IPA/chloroform (70/15/15). Flow rate, 0.8 mL/min. Detection wavelength, 254 nm. Temperature, 25 °C.
    Figure Legend Snippet: Chiral separation chromatograms of racemates on CPM2 column under normal phase mode. ( 1 ) 1-(1-naphthyl) ethanol; ( 2 ) benzoin methyl ether; ( 3 ) diclofop; ( 4 ) ranolazine; ( 5 ) metalaxyl; ( 6 ) 1-phenylethanol. Chromatographic conditions: mobile phase; ( 1 – 3 ) hexane/IPA (99.5/0.5, v / v ); ( 4 ) hexane/IPA (97/3, v / v ); ( 5 ) hexane/ethanol (97/3, v / v ); ( 6 ) hexane/IPA/chloroform (70/15/15). Flow rate, 0.8 mL/min. Detection wavelength, 254 nm. Temperature, 25 °C.

    Techniques Used: Indirect Immunoperoxidase Assay, Flow Cytometry

    Related Articles

    other:

    Article Title: Noncontact catalysis: Initiation of selective ethylbenzene oxidation by Au cluster-facilitated cyclooctene epoxidation
    Article Snippet: Chemicals and materials Sources and purities of chemicals used were as follows: HAuCl4 •3H2 O (≥99.9% trace metals basis, Sigma-Aldrich), fumed silica (CAB-O-SIL90, Cabot Corporation), ethylenediamine (≥99% ReagentPlus, Sigma-Aldrich), ethanol (200 grade, Decon Labs), cobalt(II) nitrate hexahydrate (≥98%, Sigma-Aldrich), Nano H-ZSM-5 (P-26, ACS Material), decane (≥99% ReagentPlus, Sigma-Aldrich), dodecane (≥99% ReagentPlus, Sigma-Aldrich), cis-cyclooctene (95%, Alfa Aesar), EB (99.8% anhydrous, Sigma-Aldrich), EB-d10 (99 atomic % D, Sigma-Aldrich), 4-methylanisole (99%, Sigma-Aldrich), acetophenone (99% ReagentPlus, Sigma-Aldrich), 1-phenylethanol (98%, Sigma-Aldrich), hydrogen peroxide (30% aqueous solution, Fisher Chemical), potassium hydroxide (reagent grade, 90%, Sigma-Aldrich), sodium sulfate (Food Chemicals Codex/United States Pharmacopeia–grade, Fisher Chemical), tetrahydrofuran ( > 99%, Sigma-Aldrich), tert -butyl hydroperoxide (~5.5 M in decane, Sigma-Aldrich), PPh3 ( > 98.5%, Sigma-Aldrich), d -chloroform (99.8 atomic % D, Sigma-Aldrich), HCl (38% w/w, Fisher Chemical), HNO3 (68 to 70% w/w, Fisher Chemical), EM Quant peroxide test strips, and syringe filter (polyvinylidene difluoride membrane, 0.25 mm/0.2 μm, Acrodisc).

    Article Title: Odorant receptor-based discovery of natural repellents of human lice
    Article Snippet: 4-methylcyclohexanol (98% pure), 2,3-dimethylphenol (99% pure) and 1-phenylethanol (98% pure) were purchased from Sigma-Aldrich (St. Louis, MO).

    Article Title: A comparison of semi-quantitative methods suitable for establishing volatile profiles
    Article Snippet: Normalization of peak areas of each compound was done by using 1-phenylethanol (RT 7.096, Sigma-Aldrich, ) as an internal standard by adding 10 µL (0.1%) to the sucrose solution during the flower scent analysis.

    Article Title: Increased availability of NADH in metabolically engineered baker’s yeast improves transaminase-oxidoreductase coupled asymmetric whole-cell bioconversion
    Article Snippet: Chemicals Acetophenone, racemic 1-phenylethylamine (1-PEA), and the pure enantiomers (R )-1-PEA and (S )-1-PEA, all with a purity of ≥98.0 %, were purchased from Merck (Hohenbrunn, Germany). (R )-1-phenylethanol and (S )-1-phenylethanol were purchased from Sigma-Aldrich (Steinheim, Germany), both with a purity of ≥98.0 %, and all other chemicals were from VWR (Leuven, Belgium).

    Similar Products

  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 94
    Millipore anti dcc
    Spine density and presynaptic release properties of axotomized neurons treated with exogenous netrin-1. a Representative dendrites before and 48 h post-axotomy treated with vehicle (HBS) or netrin-1 (Ntn1) beginning at 40 h post-axotomy (inverted fluorescence). Arrows : new spines; red asterisks : eliminated spines. Scale bars , 10 µm. b Quantification of spine density illustrated in a . Axotomy : n = 33 dendrites; 7 neurons; #spines/TDL: 392/3696 µm ( before ), 263/3447 µm ( after ). Axotomy + netrin-1 : n = 29 dendrites, 6 neurons; #spines/TDL: 293/3281 µm ( before ), 363/3417 µm ( after ). c Percent responsive FM puncta per neuron field at 48 h post-axotomy with HBS or netrin-1. n = 8–11 fields/chambers per condition over 5 experiments. d Number of responsive and unresponsive FM puncta from c . Significantly fewer unresponsive puncta followed axotomy compared to uninjured control (HBS). e , f Number of vGLUT1 and <t>vGAT</t> puncta per neuron area (uninjured control, axotomized + HBS, or axotomized + netrin-1) at 14 DIV. n = 8–9 neurons; 3 chambers per condition over 3 experiments. g Representative <t>DCC</t> immunostaining ( turquoise ) in uninjured control, post-axotomy, and post-axotomy + netrin-1 in cultures with similar spine densities. Neurons were retrogradely labeled with fluorescent protein (FP, magenta ) using an mCherry modified rabies virus. Scale bar , 10 µm. h Quantification of DCC immunofluorescence per spine region-of-interest (ROI). ROI: 2 µm diameter circular region surrounding each spine. Control, n = 295 ROIs; axotomy, n = 293 ROIs; axotomy + Ntn1, n = 210 ROIs. 8 neuron fields/3 chambers per condition; 3 experiments. i Quantification of spine density following 24 h of control antibody (IgG ab.) or DCC function blocking antibody (DCC ab.). IgG: n = 33 dendrites; 8 neurons; #spines/TDL: 464/4864 µm (before), 419/4712 µm (after). DCC ab: n = 34 dendrites; 7 neurons; #spines/TDL: 404/4433 µm (before), 222/3647 µm (after). j Representative FP-labeled dendritic segments immunostained for vGAT (inverted) and vGLUT1 (inverted) following 24 h application of IgG or DCC antibodies (outlined dendrites, solid magenta line ). Neurons were fixed at 15–16 DIV, older than the cultures in e , f . Scale bar , 10 µm. Quantification shown on the right. n = 23 neuron fields per condition; 3 chambers per condition over 3 experiments. b , i Repeated-measure two-way ANOVA, Bonferroni post hoc test; analyses included 1 chamber per condition for 3 experiments. c , j Unpaired two-tailed t -test. d – f , h One-way ANOVA, Bonferroni post hoc test. Error bars , s.e.m. * p
    Anti Dcc, supplied by Millipore, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti dcc/product/Millipore
    Average 94 stars, based on 3 article reviews
    Price from $9.99 to $1999.99
    anti dcc - by Bioz Stars, 2020-11
    94/100 stars
      Buy from Supplier

    90
    Millipore human tmod1 peptide
    Decreased active force production and stiffness in skinned skeletal muscle fibers from <t>Tmod1</t> −/− mice. Shown are typical peak force-length change ( A ), relative stiffness-relative force ( B ) and y 0 -force ( C ) relationships of skinned muscle fibers from Tmod1 +/+ (solid circles) and Tmod1 −/− (open circles) mice.
    Human Tmod1 Peptide, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human tmod1 peptide/product/Millipore
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    human tmod1 peptide - by Bioz Stars, 2020-11
    90/100 stars
      Buy from Supplier

    Image Search Results


    Spine density and presynaptic release properties of axotomized neurons treated with exogenous netrin-1. a Representative dendrites before and 48 h post-axotomy treated with vehicle (HBS) or netrin-1 (Ntn1) beginning at 40 h post-axotomy (inverted fluorescence). Arrows : new spines; red asterisks : eliminated spines. Scale bars , 10 µm. b Quantification of spine density illustrated in a . Axotomy : n = 33 dendrites; 7 neurons; #spines/TDL: 392/3696 µm ( before ), 263/3447 µm ( after ). Axotomy + netrin-1 : n = 29 dendrites, 6 neurons; #spines/TDL: 293/3281 µm ( before ), 363/3417 µm ( after ). c Percent responsive FM puncta per neuron field at 48 h post-axotomy with HBS or netrin-1. n = 8–11 fields/chambers per condition over 5 experiments. d Number of responsive and unresponsive FM puncta from c . Significantly fewer unresponsive puncta followed axotomy compared to uninjured control (HBS). e , f Number of vGLUT1 and vGAT puncta per neuron area (uninjured control, axotomized + HBS, or axotomized + netrin-1) at 14 DIV. n = 8–9 neurons; 3 chambers per condition over 3 experiments. g Representative DCC immunostaining ( turquoise ) in uninjured control, post-axotomy, and post-axotomy + netrin-1 in cultures with similar spine densities. Neurons were retrogradely labeled with fluorescent protein (FP, magenta ) using an mCherry modified rabies virus. Scale bar , 10 µm. h Quantification of DCC immunofluorescence per spine region-of-interest (ROI). ROI: 2 µm diameter circular region surrounding each spine. Control, n = 295 ROIs; axotomy, n = 293 ROIs; axotomy + Ntn1, n = 210 ROIs. 8 neuron fields/3 chambers per condition; 3 experiments. i Quantification of spine density following 24 h of control antibody (IgG ab.) or DCC function blocking antibody (DCC ab.). IgG: n = 33 dendrites; 8 neurons; #spines/TDL: 464/4864 µm (before), 419/4712 µm (after). DCC ab: n = 34 dendrites; 7 neurons; #spines/TDL: 404/4433 µm (before), 222/3647 µm (after). j Representative FP-labeled dendritic segments immunostained for vGAT (inverted) and vGLUT1 (inverted) following 24 h application of IgG or DCC antibodies (outlined dendrites, solid magenta line ). Neurons were fixed at 15–16 DIV, older than the cultures in e , f . Scale bar , 10 µm. Quantification shown on the right. n = 23 neuron fields per condition; 3 chambers per condition over 3 experiments. b , i Repeated-measure two-way ANOVA, Bonferroni post hoc test; analyses included 1 chamber per condition for 3 experiments. c , j Unpaired two-tailed t -test. d – f , h One-way ANOVA, Bonferroni post hoc test. Error bars , s.e.m. * p

    Journal: Nature Communications

    Article Title: Distal axotomy enhances retrograde presynaptic excitability onto injured pyramidal neurons via trans-synaptic signaling

    doi: 10.1038/s41467-017-00652-y

    Figure Lengend Snippet: Spine density and presynaptic release properties of axotomized neurons treated with exogenous netrin-1. a Representative dendrites before and 48 h post-axotomy treated with vehicle (HBS) or netrin-1 (Ntn1) beginning at 40 h post-axotomy (inverted fluorescence). Arrows : new spines; red asterisks : eliminated spines. Scale bars , 10 µm. b Quantification of spine density illustrated in a . Axotomy : n = 33 dendrites; 7 neurons; #spines/TDL: 392/3696 µm ( before ), 263/3447 µm ( after ). Axotomy + netrin-1 : n = 29 dendrites, 6 neurons; #spines/TDL: 293/3281 µm ( before ), 363/3417 µm ( after ). c Percent responsive FM puncta per neuron field at 48 h post-axotomy with HBS or netrin-1. n = 8–11 fields/chambers per condition over 5 experiments. d Number of responsive and unresponsive FM puncta from c . Significantly fewer unresponsive puncta followed axotomy compared to uninjured control (HBS). e , f Number of vGLUT1 and vGAT puncta per neuron area (uninjured control, axotomized + HBS, or axotomized + netrin-1) at 14 DIV. n = 8–9 neurons; 3 chambers per condition over 3 experiments. g Representative DCC immunostaining ( turquoise ) in uninjured control, post-axotomy, and post-axotomy + netrin-1 in cultures with similar spine densities. Neurons were retrogradely labeled with fluorescent protein (FP, magenta ) using an mCherry modified rabies virus. Scale bar , 10 µm. h Quantification of DCC immunofluorescence per spine region-of-interest (ROI). ROI: 2 µm diameter circular region surrounding each spine. Control, n = 295 ROIs; axotomy, n = 293 ROIs; axotomy + Ntn1, n = 210 ROIs. 8 neuron fields/3 chambers per condition; 3 experiments. i Quantification of spine density following 24 h of control antibody (IgG ab.) or DCC function blocking antibody (DCC ab.). IgG: n = 33 dendrites; 8 neurons; #spines/TDL: 464/4864 µm (before), 419/4712 µm (after). DCC ab: n = 34 dendrites; 7 neurons; #spines/TDL: 404/4433 µm (before), 222/3647 µm (after). j Representative FP-labeled dendritic segments immunostained for vGAT (inverted) and vGLUT1 (inverted) following 24 h application of IgG or DCC antibodies (outlined dendrites, solid magenta line ). Neurons were fixed at 15–16 DIV, older than the cultures in e , f . Scale bar , 10 µm. Quantification shown on the right. n = 23 neuron fields per condition; 3 chambers per condition over 3 experiments. b , i Repeated-measure two-way ANOVA, Bonferroni post hoc test; analyses included 1 chamber per condition for 3 experiments. c , j Unpaired two-tailed t -test. d – f , h One-way ANOVA, Bonferroni post hoc test. Error bars , s.e.m. * p

    Article Snippet: Coverslips were incubated with anti-MAP2 (1:1000; Millipore # AB5622), anti-beta tubulin III (1:2000; Aves #TUJ), anti-GAD67 (1:2000; Aves labs # GAD), anti-vGLUT1 (1:100; NeuroMab, clone N28/9, cat. #75-066), anti-vGAT (1:1000; Synaptic Systems #131 003), anti-DCC (1:100; Calbiochem #OP45), or anti-synapsin1 (1:500; Calbiochem #574778) primary antibodies in 1% blocking solution for overnight at 4 °C.

    Techniques: Fluorescence, Droplet Countercurrent Chromatography, Immunostaining, Labeling, Modification, Immunofluorescence, Blocking Assay, Two Tailed Test

    Netrin-1 triggers the dissociation of a DSCAM/DCC complex. (A) DSCAM (red) and DCC (green) proteins co-localize in precrossing commissural axons in transverse section of the E12 rat spinal cord. Lower panels are close ups (20x) of the ventral spinal cord

    Journal:

    Article Title: DSCAM is a netrin receptor that collaborates with DCC in mediating turning responses to netrin-1

    doi: 10.1016/j.cell.2008.05.030

    Figure Lengend Snippet: Netrin-1 triggers the dissociation of a DSCAM/DCC complex. (A) DSCAM (red) and DCC (green) proteins co-localize in precrossing commissural axons in transverse section of the E12 rat spinal cord. Lower panels are close ups (20x) of the ventral spinal cord

    Article Snippet: Anti-DCC (AF5, Calbiochem; 2 μg/ml), DSCAM-Fc or Fc was added to the medium 30 min before initiating the gradient.

    Techniques: Droplet Countercurrent Chromatography

    DSCAM binds netrin-1. (A) COS cells expressing DSCAM or DCC, but not Robo1 bind netrin-1 (top). Receptor expression was verified by immunocytochemistry (bottom). (B–D) Netrin-1 specifically binds to DSCAM. (B) DSCAMecto-Fc or control [(BSA)] protein

    Journal:

    Article Title: DSCAM is a netrin receptor that collaborates with DCC in mediating turning responses to netrin-1

    doi: 10.1016/j.cell.2008.05.030

    Figure Lengend Snippet: DSCAM binds netrin-1. (A) COS cells expressing DSCAM or DCC, but not Robo1 bind netrin-1 (top). Receptor expression was verified by immunocytochemistry (bottom). (B–D) Netrin-1 specifically binds to DSCAM. (B) DSCAMecto-Fc or control [(BSA)] protein

    Article Snippet: Anti-DCC (AF5, Calbiochem; 2 μg/ml), DSCAM-Fc or Fc was added to the medium 30 min before initiating the gradient.

    Techniques: Expressing, Droplet Countercurrent Chromatography, Immunocytochemistry

    DSCAM guides growth cones independent of DCC

    Journal:

    Article Title: DSCAM is a netrin receptor that collaborates with DCC in mediating turning responses to netrin-1

    doi: 10.1016/j.cell.2008.05.030

    Figure Lengend Snippet: DSCAM guides growth cones independent of DCC

    Article Snippet: Anti-DCC (AF5, Calbiochem; 2 μg/ml), DSCAM-Fc or Fc was added to the medium 30 min before initiating the gradient.

    Techniques: Droplet Countercurrent Chromatography

    Decreased active force production and stiffness in skinned skeletal muscle fibers from Tmod1 −/− mice. Shown are typical peak force-length change ( A ), relative stiffness-relative force ( B ) and y 0 -force ( C ) relationships of skinned muscle fibers from Tmod1 +/+ (solid circles) and Tmod1 −/− (open circles) mice.

    Journal: The FASEB Journal

    Article Title: Pointed-end capping by tropomodulin modulates actomyosin crossbridge formation in skeletal muscle fibers

    doi: 10.1096/fj.13-239640

    Figure Lengend Snippet: Decreased active force production and stiffness in skinned skeletal muscle fibers from Tmod1 −/− mice. Shown are typical peak force-length change ( A ), relative stiffness-relative force ( B ) and y 0 -force ( C ) relationships of skinned muscle fibers from Tmod1 +/+ (solid circles) and Tmod1 −/− (open circles) mice.

    Article Snippet: For Western blotting, primary antibodies were rabbit polyclonal antiserum to residues 340–359 of a human Tmod1 peptide (PA2211, 1:5000; ref. ), rabbit polyclonal antiserum to chicken Tmod4 preadsorbed by passage through a Tmod1 Sepharose column (R3577bl3c, 1:2500; ref. ), mouse monoclonal anti-actin (C4, 1:10000; EMD Millipore, Billerica, MA, USA), and mouse monoclonal anti-tropomyosin (CH1, 1:500; Santa Cruz Biotechnology, Dallas, TX, USA).

    Techniques: Mouse Assay