1 hexanol  (Thermo Fisher)


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    Structured Review

    Thermo Fisher 1 hexanol
    1 Hexanol, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/1 hexanol/product/Thermo Fisher
    Average 90 stars, based on 3 article reviews
    Price from $9.99 to $1999.99
    1 hexanol - by Bioz Stars, 2020-09
    90/100 stars

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    other:

    Article Title: Anti-tumor Efficiency of Lipid-coated Cisplatin Nanoparticles Co-loaded with MicroRNA-375
    Article Snippet: 1-Hexanol was purchased from Alfa Aesar (Ward Hill, MA, USA).

    Article Title: Horseradish Peroxidase-Encapsulated Hollow Silica Nanospheres for Intracellular Sensing of Reactive Oxygen Species
    Article Snippet: Decane, n -hexanol (98%), ammonium hydroxide (NH4 OH, 35 wt%), tetraethyl orthosilicate (TEOS, 98%), 3-aminopropyltrimethoxysilane (APTMS, 95%), and fluorescein isothiocyanate (FITC) isomer were purchased from ACROS.

    Article Title: The Common Natural Products (S)-α-Terpineol and (E)-2-Hexenol are Important Pheromone Components of Megacyllene antennata (Coleoptera: Cerambycidae)
    Article Snippet: All compounds were purchased from commercial suppliers: ( R )- and ( S )-α-terpineol (both > 98% pure), ( E )-2-hexenol (96%), ( E )-2-hexenal (98%), ( R )- and ( S )-limonene (both 96%), and 2-phenylethanol (98%) from Sigma-Aldrich (St. Louis, MO); ( R )- and ( S )-1-phenylethanol (both > 97%) and 1-hexanol (99%) from Alfa Aesar (Ward Hill, MA); and terpinolene (85%) from TCI America (Portland, OR).

    Article Title: The effect of hydrogen bonding on the diffusion of water in n-alkanes and n-alcohols measured with a novel single microdroplet method
    Article Snippet: The materials used were n -butanol (EMD Biosciences), n -pentanol (Sigma Aldrich), n -hexanol (Acros Organics), n -heptanol (Sigma Aldrich), n -octanol (Sigma Aldrich), n -pentane (Burdick & Jackson), n -hexane (Sigma Aldrich), n -heptane (Sigma Aldrich), n -octane (Sigma Aldrich), n -decane (TCI America), n -undecane (Sigma Aldrich), n -tetradecane (Sigma Aldrich), n -hexadecane (Sigma Aldrich), and de-ionized water.

    Article Title: Characterization of the Key Aroma Compounds in Three Truffle Varieties from China by Flavoromics Approach
    Article Snippet: Chemicals 2-methylbutanal, 3-methylbutanal, pentanal, isopropyl alcohol, 1-propanol, 1-butanol, hexanal, 2-methyl-1-propanol, (E )-2-methyl-2-butenal, limonene, heptenal, 2-butenal, 2-methylbutanol, 3-methylbutanol, 2-pentyl-furan, 3-octanone, 1-pentanol, 2-octanone, 4-isopropyltoluene, octanal, 1-octen-3-one, isobutyl hexanoate, nonanal, heptanoic acid ethyl ester, 1-hexanol, 3-octanol, octanoic acid ethyl ester, (E )-2-octenal, (E )-2-nonenal, P-cresyl methyl ether, 1-heptanol, 1-octen-3-ol, 1-octanol, benzaldehyde, 2-methyl-butanoic acid, 3-methyl-butanoic acid, 2-acetylthiazole, benzeneacetaldehyde, benzyl alcohol, phenylethyl alcohol, γ-nonalactone, were purchased from Alfa Aesar Corporation (Tianjin, China).

    Article Title: Horseradish Peroxidase-Encapsulated Hollow Silica Nanospheres for Intracellular Sensing of Reactive Oxygen Species
    Article Snippet: Chemicals and Reagents Decane, n -hexanol (98%), ammonium hydroxide (NH4 OH, 35 wt%), tetraethyl orthosilicate (TEOS, 98%), 3-aminopropyltrimethoxysilane (APTMS, 95%), and fluorescein isothiocyanate (FITC) isomer were purchased from ACROS.

    Article Title: Synthesis of silica-alginate nanoparticles and their potential application as pH-responsive drug carriers
    Article Snippet: Sodium alginate (very low viscosity) and n-hexanol, were purchased from Alfa Aesar (Massachusetts, USA).

    Article Title: Turning a Water And Oil Insoluble Cisplatin Derivative into a Nanoparticle Formulation for Cancer Therapy
    Article Snippet: 1-Hexanol was purchased from Alfa Aesar.

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    Thermo Fisher biotin x dhpe lipids
    Single <t>Biotin-X-DHPE</t> molecules tagged with Streptavidin-Alexa546 were tracked on the curved supported lipid bilayers (ROC = 28 nm) in space and time. ( a ) example trajectories (blue) show the heterogeneous dynamics observed on both flat (white) and curved (black) regions. Scale bar = 1 µm; ( b ) the average step a molecule takes over 0.228 s (5 frames) when starting at a region of curvature (white) or at a flat region (grey); ( c ) the distribution of steps observed at curved and flat regions (shown in Figure S3 ) was fitted to Equation 3 to obtain the diffusion coefficients and the percentage of steps moving at that rate. The average D is plotted for t = 0.091, 0.228 and 0.456. Note that there is no fast component for the tracks that start at regions of curvature.
    Biotin X Dhpe Lipids, supplied by Thermo Fisher, 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/biotin x dhpe lipids/product/Thermo Fisher
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    biotin x dhpe lipids - by Bioz Stars, 2020-09
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    95
    Thermo Fisher c6 ceramide
    Glutamate uptake is not altered in Cln3 Δex7/8 astrocytes. Primary WT and Cln3 Δex7/8 astrocytes were treated with TNF-α and IL-1β (10ng/mL each) or <t>C6</t> ceramide (5μM) and neuronal lysate (NL) for 24 h. Cells were then exposed to 1mM glutamate, whereupon supernatants were collected 30 min and 2 h later to evaluate residual extracellular glutamate concentrations. Results were normalized to the 1mM glutamate control and are presented as the mean ± standard error of the mean (SEM) combined from three independent experiments with a total of 3 biological replicates.
    C6 Ceramide, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/c6 ceramide/product/Thermo Fisher
    Average 95 stars, based on 3 article reviews
    Price from $9.99 to $1999.99
    c6 ceramide - by Bioz Stars, 2020-09
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    99
    Thermo Fisher sulfo nhs lc biotin
    Effects of mutations in the hBest1 C terminus on channel function. (A) Current amplitudes of point mutants in the C-terminal acidic region (amino acids 293–308) and the putative EF hand loop (amino acids 312–323). Each amino acid (in black) and its position in the C terminus are indicated along the axis. The corresponding mutations are colored red, green, and blue. Each data point represents four to nine cells. The solid line indicates the average current amplitude of wild type ( n = 8), and the dashed lines represent the standard error. (B) Expression of hBest1 mutants in the plasma membrane of HEK cells. Wild-type, N296L, E300Q, D301N, D302N, D303L, D304N, E306Q, and N308D mutant-transfected and nontransfected cells were exposed to membrane-impermeable <t>Sulfo-NHS-LC</t> biotin. <t>Biotinylated</t> membrane proteins (20 μl; left) purified with streptavidin resin and total proteins (5 μl; right) were probed with antibodies to the myc tag on hBest1 (68-kD band; top) and with antibodies to intracellular protein GAPDH (37-kD band; bottom).
    Sulfo Nhs Lc Biotin, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 26 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sulfo nhs lc biotin/product/Thermo Fisher
    Average 99 stars, based on 26 article reviews
    Price from $9.99 to $1999.99
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    Image Search Results


    Single Biotin-X-DHPE molecules tagged with Streptavidin-Alexa546 were tracked on the curved supported lipid bilayers (ROC = 28 nm) in space and time. ( a ) example trajectories (blue) show the heterogeneous dynamics observed on both flat (white) and curved (black) regions. Scale bar = 1 µm; ( b ) the average step a molecule takes over 0.228 s (5 frames) when starting at a region of curvature (white) or at a flat region (grey); ( c ) the distribution of steps observed at curved and flat regions (shown in Figure S3 ) was fitted to Equation 3 to obtain the diffusion coefficients and the percentage of steps moving at that rate. The average D is plotted for t = 0.091, 0.228 and 0.456. Note that there is no fast component for the tracks that start at regions of curvature.

    Journal: Membranes

    Article Title: Single Lipid Molecule Dynamics on Supported Lipid Bilayers with Membrane Curvature

    doi: 10.3390/membranes7010015

    Figure Lengend Snippet: Single Biotin-X-DHPE molecules tagged with Streptavidin-Alexa546 were tracked on the curved supported lipid bilayers (ROC = 28 nm) in space and time. ( a ) example trajectories (blue) show the heterogeneous dynamics observed on both flat (white) and curved (black) regions. Scale bar = 1 µm; ( b ) the average step a molecule takes over 0.228 s (5 frames) when starting at a region of curvature (white) or at a flat region (grey); ( c ) the distribution of steps observed at curved and flat regions (shown in Figure S3 ) was fitted to Equation 3 to obtain the diffusion coefficients and the percentage of steps moving at that rate. The average D is plotted for t = 0.091, 0.228 and 0.456. Note that there is no fast component for the tracks that start at regions of curvature.

    Article Snippet: The dynamics of Biotin-X-DHPE lipids were detected by in situ labeling with Alexa Fluor 546 (Thermo Fisher) conjugated to streptavidin (Strep-546).

    Techniques: Diffusion-based Assay

    Glutamate uptake is not altered in Cln3 Δex7/8 astrocytes. Primary WT and Cln3 Δex7/8 astrocytes were treated with TNF-α and IL-1β (10ng/mL each) or C6 ceramide (5μM) and neuronal lysate (NL) for 24 h. Cells were then exposed to 1mM glutamate, whereupon supernatants were collected 30 min and 2 h later to evaluate residual extracellular glutamate concentrations. Results were normalized to the 1mM glutamate control and are presented as the mean ± standard error of the mean (SEM) combined from three independent experiments with a total of 3 biological replicates.

    Journal: Journal of neurochemistry

    Article Title: Astrocytes in Juvenile Neuronal Ceroid Lipofuscinosis (CLN3) display metabolic and calcium signaling abnormalities

    doi: 10.1111/jnc.14545

    Figure Lengend Snippet: Glutamate uptake is not altered in Cln3 Δex7/8 astrocytes. Primary WT and Cln3 Δex7/8 astrocytes were treated with TNF-α and IL-1β (10ng/mL each) or C6 ceramide (5μM) and neuronal lysate (NL) for 24 h. Cells were then exposed to 1mM glutamate, whereupon supernatants were collected 30 min and 2 h later to evaluate residual extracellular glutamate concentrations. Results were normalized to the 1mM glutamate control and are presented as the mean ± standard error of the mean (SEM) combined from three independent experiments with a total of 3 biological replicates.

    Article Snippet: Primary WT and Cln3 Δex7/8 astrocytes were seeded at 2x104 cells per well in 96-well plates and incubated for 12 h prior to treatment with combinations of TNF-α and IL-1β (10ng/ml each) or C6 ceramide (5μM) and neuronal lysate (1:5 dilution) for 24 h. To examine glutamate uptake efficiency, astrocytes were exposed to 1mM glutamic acid in phenol red-free DMEM (ThermoFisher; Cat. #31053-028), whereupon supernatants were collected at 30 min and 2 h following glutamate treatment.

    Techniques:

    CLN3 mutation does not affect astrocyte glycolytic activity. Primary WT and Cln3 Δex7/8 astrocytes were unstimulated or treated with TNF-α and IL-1β (10ng/mL each) or C6 ceramide (5μM) and neuronal lysate (NL) for 24 h, whereupon glycolytic activity was examined using Seahorse Bioscience assays. (A) Glycolysis, (B) Maximum capacity, and (C) Glycolytic reserve was determined based on extracellular acidification rate (ECAR). Results are representative of three independent experiments with a total of 3 biological replicates (mean ± standard error of the mean (SEM).

    Journal: Journal of neurochemistry

    Article Title: Astrocytes in Juvenile Neuronal Ceroid Lipofuscinosis (CLN3) display metabolic and calcium signaling abnormalities

    doi: 10.1111/jnc.14545

    Figure Lengend Snippet: CLN3 mutation does not affect astrocyte glycolytic activity. Primary WT and Cln3 Δex7/8 astrocytes were unstimulated or treated with TNF-α and IL-1β (10ng/mL each) or C6 ceramide (5μM) and neuronal lysate (NL) for 24 h, whereupon glycolytic activity was examined using Seahorse Bioscience assays. (A) Glycolysis, (B) Maximum capacity, and (C) Glycolytic reserve was determined based on extracellular acidification rate (ECAR). Results are representative of three independent experiments with a total of 3 biological replicates (mean ± standard error of the mean (SEM).

    Article Snippet: Primary WT and Cln3 Δex7/8 astrocytes were seeded at 2x104 cells per well in 96-well plates and incubated for 12 h prior to treatment with combinations of TNF-α and IL-1β (10ng/ml each) or C6 ceramide (5μM) and neuronal lysate (1:5 dilution) for 24 h. To examine glutamate uptake efficiency, astrocytes were exposed to 1mM glutamic acid in phenol red-free DMEM (ThermoFisher; Cat. #31053-028), whereupon supernatants were collected at 30 min and 2 h following glutamate treatment.

    Techniques: Mutagenesis, Activity Assay

    Mitochondrial respiration is impaired in Cln3 Δex7/8 astrocytes. Primary WT and Cln3 Δex7/8 astrocytes were unstimulated or treated with TNF-α and IL-1β (10ng/mL each) or C6 ceramide (5μM) and neuronal lysate (NL) for 24 h, whereupon oxidative phosphorylation (Ox Phos) activity was examined using Seahorse Bioscience assays. (A) Basal mitochondrial respiration and (B) ATP production was determined based on oxygen consumption rate (OCR). Results are representative of three independent experiments with a total of 3 biological replicates (mean ± standard error of the mean (SEM). (C) Mitochondrial biomass was determined by quantiating NADH dehydrogenase 3 (ND3) and cytochrome c oxidase subunit-1 (Cox-1) expressed as a ratio to genomic DNA. Results are presented as the mean ± SEM of 4 biological replicates. Significant differences between WT and Cln3 Δex7/8 astrocytes are denoted by asterisks (*, p

    Journal: Journal of neurochemistry

    Article Title: Astrocytes in Juvenile Neuronal Ceroid Lipofuscinosis (CLN3) display metabolic and calcium signaling abnormalities

    doi: 10.1111/jnc.14545

    Figure Lengend Snippet: Mitochondrial respiration is impaired in Cln3 Δex7/8 astrocytes. Primary WT and Cln3 Δex7/8 astrocytes were unstimulated or treated with TNF-α and IL-1β (10ng/mL each) or C6 ceramide (5μM) and neuronal lysate (NL) for 24 h, whereupon oxidative phosphorylation (Ox Phos) activity was examined using Seahorse Bioscience assays. (A) Basal mitochondrial respiration and (B) ATP production was determined based on oxygen consumption rate (OCR). Results are representative of three independent experiments with a total of 3 biological replicates (mean ± standard error of the mean (SEM). (C) Mitochondrial biomass was determined by quantiating NADH dehydrogenase 3 (ND3) and cytochrome c oxidase subunit-1 (Cox-1) expressed as a ratio to genomic DNA. Results are presented as the mean ± SEM of 4 biological replicates. Significant differences between WT and Cln3 Δex7/8 astrocytes are denoted by asterisks (*, p

    Article Snippet: Primary WT and Cln3 Δex7/8 astrocytes were seeded at 2x104 cells per well in 96-well plates and incubated for 12 h prior to treatment with combinations of TNF-α and IL-1β (10ng/ml each) or C6 ceramide (5μM) and neuronal lysate (1:5 dilution) for 24 h. To examine glutamate uptake efficiency, astrocytes were exposed to 1mM glutamic acid in phenol red-free DMEM (ThermoFisher; Cat. #31053-028), whereupon supernatants were collected at 30 min and 2 h following glutamate treatment.

    Techniques: Activity Assay

    Effects of mutations in the hBest1 C terminus on channel function. (A) Current amplitudes of point mutants in the C-terminal acidic region (amino acids 293–308) and the putative EF hand loop (amino acids 312–323). Each amino acid (in black) and its position in the C terminus are indicated along the axis. The corresponding mutations are colored red, green, and blue. Each data point represents four to nine cells. The solid line indicates the average current amplitude of wild type ( n = 8), and the dashed lines represent the standard error. (B) Expression of hBest1 mutants in the plasma membrane of HEK cells. Wild-type, N296L, E300Q, D301N, D302N, D303L, D304N, E306Q, and N308D mutant-transfected and nontransfected cells were exposed to membrane-impermeable Sulfo-NHS-LC biotin. Biotinylated membrane proteins (20 μl; left) purified with streptavidin resin and total proteins (5 μl; right) were probed with antibodies to the myc tag on hBest1 (68-kD band; top) and with antibodies to intracellular protein GAPDH (37-kD band; bottom).

    Journal: The Journal of General Physiology

    Article Title: Regulation of Bestrophin Cl Channels by Calcium: Role of the C Terminus

    doi: 10.1085/jgp.200810056

    Figure Lengend Snippet: Effects of mutations in the hBest1 C terminus on channel function. (A) Current amplitudes of point mutants in the C-terminal acidic region (amino acids 293–308) and the putative EF hand loop (amino acids 312–323). Each amino acid (in black) and its position in the C terminus are indicated along the axis. The corresponding mutations are colored red, green, and blue. Each data point represents four to nine cells. The solid line indicates the average current amplitude of wild type ( n = 8), and the dashed lines represent the standard error. (B) Expression of hBest1 mutants in the plasma membrane of HEK cells. Wild-type, N296L, E300Q, D301N, D302N, D303L, D304N, E306Q, and N308D mutant-transfected and nontransfected cells were exposed to membrane-impermeable Sulfo-NHS-LC biotin. Biotinylated membrane proteins (20 μl; left) purified with streptavidin resin and total proteins (5 μl; right) were probed with antibodies to the myc tag on hBest1 (68-kD band; top) and with antibodies to intracellular protein GAPDH (37-kD band; bottom).

    Article Snippet: In brief, cells transfected with wild-type and mutant hBest1 and nontransfected cells were placed on ice, washed three times with PBS, and biotinylated with 0.5 mg/ml Sulfo-NHS-LC Biotin (Thermo Fisher Scientific) in PBS for 30 min.

    Techniques: Expressing, Mutagenesis, Transfection, Purification

    Cell-surface labeling with biotin. The surface proteins of P. gingivalis and T. forsythia were labeled with Sulfo-NHS-LC-Biotin and mixed with T. forsythia and P. gingivalis cells, respectively. Subsequently, the mixtures were subjected to SDS-PAGE, and then transferred onto nitrocellulose membranes. Biotinylated P. gingivalis and T. forsythia surface proteins were detected with streptavidin–HRP and 4-CN. Lanes: MW, molecular weight marker; Tf, biotinylated T. forsythia surface proteins bound to P. gingivalis ; Pg, biotinylated P. gingivalis surface proteins bound to T. forsythia

    Journal: Journal of Periodontal & Implant Science

    Article Title: Surface interactions between two of the main periodontal pathogens: Porphyromonas gingivalis and Tannerella forsythia

    doi: 10.5051/jpis.2016.46.1.2

    Figure Lengend Snippet: Cell-surface labeling with biotin. The surface proteins of P. gingivalis and T. forsythia were labeled with Sulfo-NHS-LC-Biotin and mixed with T. forsythia and P. gingivalis cells, respectively. Subsequently, the mixtures were subjected to SDS-PAGE, and then transferred onto nitrocellulose membranes. Biotinylated P. gingivalis and T. forsythia surface proteins were detected with streptavidin–HRP and 4-CN. Lanes: MW, molecular weight marker; Tf, biotinylated T. forsythia surface proteins bound to P. gingivalis ; Pg, biotinylated P. gingivalis surface proteins bound to T. forsythia

    Article Snippet: Confirmation of biotin-labeled surface proteins bound to P. gingivalis and T. forsythia cells The surface proteins of T. forsythia and P. gingivalis cells were labeled with Sulfo-NHS-LC-Biotin.

    Techniques: Labeling, SDS Page, Molecular Weight, Marker