2 bromo 1 phenylethanone  (Millipore)


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  • 98
    Name:
    2 Dimethylamino 1 phenylethanone hydrochloride
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    Catalog Number:
    otv000837
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    Millipore 2 bromo 1 phenylethanone
    2 Dimethylamino 1 phenylethanone hydrochloride

    https://www.bioz.com/result/2 bromo 1 phenylethanone/product/Millipore
    Average 98 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    2 bromo 1 phenylethanone - by Bioz Stars, 2020-11
    98/100 stars

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    Article Snippet: .. An advanced approach with DNA-mediated bismuth tungstate (Bi < sub > 2 < /sub > WO < sub > 6 < /sub > ) one-dimensional (1-D) nanochain assemblies for hydrogen production with 5-fold enhanced photoelectrochemical (PEC) water splitting reaction is presented. ..

    other:

    Article Title: Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity
    Article Snippet: The reagents 2-bromo-1-phenylethanone (98%), 2-bromo-1-(4-methoxyphenyl)ethanone (97%), 2-bromo-1-(4-chlorophenyl)ethanone (98%), 2-bromo-1-(4-bromophenyl)ethanone (98%), 2-bromo-1-(4-fluorinephenyl)ethanone (98%), 2-bromo-1-(3-fluorinephenyl)ethanone (98%), (+)-sodium L-ascorbate (98%) and ethinylestradiol (≥98%) were purchased from Sigma-Aldrich.

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  • 96
    Millipore salbutamol increased smn protein levels
    Co-immunoprecipitation (co-IP) experiments in HeLa cells. Ubiquitinated <t>SMN</t> protein was determined by co-IP using anti-SMN antibody. (A) Ubiquitinated SMN extracted by co-IP. HeLa cells were incubated with <t>salbutamol</t> sulfate (20 µM) for 24 h in the presence or absence of the proteasome inhibitor, MG132 (5 µM). SMN ubiquitination was reduced in HeLa cells treated with salbutamol, in the presence or absence of MG132. (B) Quantification of ubiquitinated SMN levels. The amount of ubiquitinated SMN at the mock status (not treated with salbutamol) was normalized to 1.0 in each MG132 group (in the presence or absence of MG132). The mean ubiquitinated SMN amount decreased by 20–30 percent after salbutamol treatment.
    Salbutamol Increased Smn Protein Levels, supplied by Millipore, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    97
    Millipore salbutamol sulfate
    Effect of several inhaled drugs on multidrug resistance-associated protein-1 (MRP1) activity and expression. (A) Efflux studies from alveolar type 1-like (AT1-like) cell monolayers show significant and dose-dependent reduction of carboxyfluorescein (CF) efflux in the presence of budesonide. (B) Immunoblot analysis shows that treatment of NCI-H441 cells with budesonide (5 or 10 μM) or <t>salbutamol</t> sulfate (100 μM) for up to 6 days has no effect on MRP1 abundance. Data are represented as means + SD, n ≥ 6, ** P ≤ 0.01, *** P ≤ 0.001. One-way ANOVA followed by Bonferroni’s post hoc comparisons test was used.
    Salbutamol Sulfate, supplied by Millipore, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    89
    Millipore 2 phenylethanol
    Tetanus toxin-mediated silencing of HDB disrupts odor habituation and discrimination without affecting general cognitive abilities. (A) Schematic of the stereotaxic injection. (B) The odor habituation/discrimination test (OHOD) performed in an open-field arena (60 x 60 cm). The circle in the middle of the arena indicates a petri dish containing a paper with odorant covered with fresh bedding. <t>2-phenylethanol</t> (rose odor) and vanillin were used in habituation and discrimination trials, accordingly. (C) Investigation time (time spent at petri dish, 120 or 240 sec trial duration and 2 min. ITI) of control and HDB silenced mice during odor habituation and discrimination trials (see also Fig. 1 ). (D) Schematic of the stereotaxic injection. (E) Latency (time to reach the petri dish) and investigation time of control and HDB silenced mice during odor habituation and discrimination trials with shorter trial durations. (F) Schematic stereotaxic injection and sequence of experiments. (G) Latency and Investigation time of control and HDB silenced mice during odor habituation and discrimination trials before (blue) and after TeTn virus injection. (H) Schematic of test sequence and stereotaxic injection. (I) Buried food test was conducted in home cage. The ellipse indicates a hidden food pellet. (J) Latency in finding the food pellet of control and HDB silenced mice during buried food test. (K) The puzzle box test paradigm. Left: the arena is divided by black-painted Plexiglas into the start and goal compartments. Right: a timeline of the experiment; the compartments are connected by a door opening (trial 1), open underpass (trials 2-4), underpass blocked by sawdust (trials 5-7), or underpass blocked by a cardboard plug (trials 8-10). (L) Latency (time to enter the goal compartment) of control and HDB silenced mice. 1-way ANOVA followed by Dunnett’s posttest (*) and t-test (#) of sham-injected (n=6) and TeTn-injected (n=6) mice. #, *p
    2 Phenylethanol, supplied by Millipore, used in various techniques. Bioz Stars score: 89/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Co-immunoprecipitation (co-IP) experiments in HeLa cells. Ubiquitinated SMN protein was determined by co-IP using anti-SMN antibody. (A) Ubiquitinated SMN extracted by co-IP. HeLa cells were incubated with salbutamol sulfate (20 µM) for 24 h in the presence or absence of the proteasome inhibitor, MG132 (5 µM). SMN ubiquitination was reduced in HeLa cells treated with salbutamol, in the presence or absence of MG132. (B) Quantification of ubiquitinated SMN levels. The amount of ubiquitinated SMN at the mock status (not treated with salbutamol) was normalized to 1.0 in each MG132 group (in the presence or absence of MG132). The mean ubiquitinated SMN amount decreased by 20–30 percent after salbutamol treatment.

    Journal: Biochemistry and Biophysics Reports

    Article Title: Salbutamol inhibits ubiquitin-mediated survival motor neuron protein degradation in spinal muscular atrophy cells

    doi: 10.1016/j.bbrep.2015.10.012

    Figure Lengend Snippet: Co-immunoprecipitation (co-IP) experiments in HeLa cells. Ubiquitinated SMN protein was determined by co-IP using anti-SMN antibody. (A) Ubiquitinated SMN extracted by co-IP. HeLa cells were incubated with salbutamol sulfate (20 µM) for 24 h in the presence or absence of the proteasome inhibitor, MG132 (5 µM). SMN ubiquitination was reduced in HeLa cells treated with salbutamol, in the presence or absence of MG132. (B) Quantification of ubiquitinated SMN levels. The amount of ubiquitinated SMN at the mock status (not treated with salbutamol) was normalized to 1.0 in each MG132 group (in the presence or absence of MG132). The mean ubiquitinated SMN amount decreased by 20–30 percent after salbutamol treatment.

    Article Snippet: SMN2 transcript levels were measured at 0 m (pretreatment), 5 m, 15 m, 30 m, 1 h, 2 h, 4 h, 8 h, 12 h, 24 h and 36 h. SMN protein levels were measured at 0 h (pretreatment), 1 h, 6 h, 8 h, 12 h, 24 h and 36 h. The mechanism whereby salbutamol increased SMN protein levels was further investigated by adding PKA inhibitor 14–22 amide cell-permeable, myristoylated (Calbiochem; Darmstadt, Germany) (final concentration; 1 µM) and DUB inhibitor PR-619 (LifeSensors, Malvern, PA, USA) (final concentration; 10 µM), respectively, to SMA fibroblast cells with salbutamol (final concentration; 0.5 µM), and incubating for 36 h.

    Techniques: Immunoprecipitation, Co-Immunoprecipitation Assay, Incubation

    SMN protein expression in salbutamol-treated SMA fibroblast cells. Salbutamol concentrations used in this study were 0.005, 0.05 and 0.5 µM. Measurement time points were 0 h, 1 h, 6 h, 8 h, 12 h, 24 h and 36 h. (A) Western blotting analysis of SMN protein in SMA fibroblast cells. (B) Relative SMN protein levels in salbutamol-treated SMA fibroblast cells. Salbutamol increased SMN protein levels in dose- and time-dependent manners. (C) Effect of PKA inhibitor on SMN protein levels. PKA inhibitor, 14–22 amide cell-permeable, myristoylated, completely repressed the salbutamol (0.5 µM)-induced increase of SMN protein.

    Journal: Biochemistry and Biophysics Reports

    Article Title: Salbutamol inhibits ubiquitin-mediated survival motor neuron protein degradation in spinal muscular atrophy cells

    doi: 10.1016/j.bbrep.2015.10.012

    Figure Lengend Snippet: SMN protein expression in salbutamol-treated SMA fibroblast cells. Salbutamol concentrations used in this study were 0.005, 0.05 and 0.5 µM. Measurement time points were 0 h, 1 h, 6 h, 8 h, 12 h, 24 h and 36 h. (A) Western blotting analysis of SMN protein in SMA fibroblast cells. (B) Relative SMN protein levels in salbutamol-treated SMA fibroblast cells. Salbutamol increased SMN protein levels in dose- and time-dependent manners. (C) Effect of PKA inhibitor on SMN protein levels. PKA inhibitor, 14–22 amide cell-permeable, myristoylated, completely repressed the salbutamol (0.5 µM)-induced increase of SMN protein.

    Article Snippet: SMN2 transcript levels were measured at 0 m (pretreatment), 5 m, 15 m, 30 m, 1 h, 2 h, 4 h, 8 h, 12 h, 24 h and 36 h. SMN protein levels were measured at 0 h (pretreatment), 1 h, 6 h, 8 h, 12 h, 24 h and 36 h. The mechanism whereby salbutamol increased SMN protein levels was further investigated by adding PKA inhibitor 14–22 amide cell-permeable, myristoylated (Calbiochem; Darmstadt, Germany) (final concentration; 1 µM) and DUB inhibitor PR-619 (LifeSensors, Malvern, PA, USA) (final concentration; 10 µM), respectively, to SMA fibroblast cells with salbutamol (final concentration; 0.5 µM), and incubating for 36 h.

    Techniques: Expressing, Western Blot

    Effect of deubiquitinase (DUB) inhibitor on SMN protein levels. Salbutamol concentration used in this study was 0.5 µM. Measurement time points were 0 h, 1 h, 6 h, 8 h, 12 h, 24 h and 36 h. The DUB inhibitor, PR-619, partially repressed the salbutamol -induced increase of SMN protein.

    Journal: Biochemistry and Biophysics Reports

    Article Title: Salbutamol inhibits ubiquitin-mediated survival motor neuron protein degradation in spinal muscular atrophy cells

    doi: 10.1016/j.bbrep.2015.10.012

    Figure Lengend Snippet: Effect of deubiquitinase (DUB) inhibitor on SMN protein levels. Salbutamol concentration used in this study was 0.5 µM. Measurement time points were 0 h, 1 h, 6 h, 8 h, 12 h, 24 h and 36 h. The DUB inhibitor, PR-619, partially repressed the salbutamol -induced increase of SMN protein.

    Article Snippet: SMN2 transcript levels were measured at 0 m (pretreatment), 5 m, 15 m, 30 m, 1 h, 2 h, 4 h, 8 h, 12 h, 24 h and 36 h. SMN protein levels were measured at 0 h (pretreatment), 1 h, 6 h, 8 h, 12 h, 24 h and 36 h. The mechanism whereby salbutamol increased SMN protein levels was further investigated by adding PKA inhibitor 14–22 amide cell-permeable, myristoylated (Calbiochem; Darmstadt, Germany) (final concentration; 1 µM) and DUB inhibitor PR-619 (LifeSensors, Malvern, PA, USA) (final concentration; 10 µM), respectively, to SMA fibroblast cells with salbutamol (final concentration; 0.5 µM), and incubating for 36 h.

    Techniques: Concentration Assay

    Effect of several inhaled drugs on multidrug resistance-associated protein-1 (MRP1) activity and expression. (A) Efflux studies from alveolar type 1-like (AT1-like) cell monolayers show significant and dose-dependent reduction of carboxyfluorescein (CF) efflux in the presence of budesonide. (B) Immunoblot analysis shows that treatment of NCI-H441 cells with budesonide (5 or 10 μM) or salbutamol sulfate (100 μM) for up to 6 days has no effect on MRP1 abundance. Data are represented as means + SD, n ≥ 6, ** P ≤ 0.01, *** P ≤ 0.001. One-way ANOVA followed by Bonferroni’s post hoc comparisons test was used.

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Tobacco Smoke and Inhaled Drugs Alter Expression and Activity of Multidrug Resistance-Associated Protein-1 (MRP1) in Human Distal Lung Epithelial Cells in vitro

    doi: 10.3389/fbioe.2020.01030

    Figure Lengend Snippet: Effect of several inhaled drugs on multidrug resistance-associated protein-1 (MRP1) activity and expression. (A) Efflux studies from alveolar type 1-like (AT1-like) cell monolayers show significant and dose-dependent reduction of carboxyfluorescein (CF) efflux in the presence of budesonide. (B) Immunoblot analysis shows that treatment of NCI-H441 cells with budesonide (5 or 10 μM) or salbutamol sulfate (100 μM) for up to 6 days has no effect on MRP1 abundance. Data are represented as means + SD, n ≥ 6, ** P ≤ 0.01, *** P ≤ 0.001. One-way ANOVA followed by Bonferroni’s post hoc comparisons test was used.

    Article Snippet: In addition, the analysis was used to determine the effect of CSE, budesonide and salbutamol sulfate on MRP1 abundance in NCI-H441 cells.

    Techniques: Activity Assay, Expressing

    Tetanus toxin-mediated silencing of HDB disrupts odor habituation and discrimination without affecting general cognitive abilities. (A) Schematic of the stereotaxic injection. (B) The odor habituation/discrimination test (OHOD) performed in an open-field arena (60 x 60 cm). The circle in the middle of the arena indicates a petri dish containing a paper with odorant covered with fresh bedding. 2-phenylethanol (rose odor) and vanillin were used in habituation and discrimination trials, accordingly. (C) Investigation time (time spent at petri dish, 120 or 240 sec trial duration and 2 min. ITI) of control and HDB silenced mice during odor habituation and discrimination trials (see also Fig. 1 ). (D) Schematic of the stereotaxic injection. (E) Latency (time to reach the petri dish) and investigation time of control and HDB silenced mice during odor habituation and discrimination trials with shorter trial durations. (F) Schematic stereotaxic injection and sequence of experiments. (G) Latency and Investigation time of control and HDB silenced mice during odor habituation and discrimination trials before (blue) and after TeTn virus injection. (H) Schematic of test sequence and stereotaxic injection. (I) Buried food test was conducted in home cage. The ellipse indicates a hidden food pellet. (J) Latency in finding the food pellet of control and HDB silenced mice during buried food test. (K) The puzzle box test paradigm. Left: the arena is divided by black-painted Plexiglas into the start and goal compartments. Right: a timeline of the experiment; the compartments are connected by a door opening (trial 1), open underpass (trials 2-4), underpass blocked by sawdust (trials 5-7), or underpass blocked by a cardboard plug (trials 8-10). (L) Latency (time to enter the goal compartment) of control and HDB silenced mice. 1-way ANOVA followed by Dunnett’s posttest (*) and t-test (#) of sham-injected (n=6) and TeTn-injected (n=6) mice. #, *p

    Journal: bioRxiv

    Article Title: The diagonal band of broca continually regulates olfactory-mediated behaviors by modulating odor-evoked responses within the olfactory bulb

    doi: 10.1101/2020.11.07.372649

    Figure Lengend Snippet: Tetanus toxin-mediated silencing of HDB disrupts odor habituation and discrimination without affecting general cognitive abilities. (A) Schematic of the stereotaxic injection. (B) The odor habituation/discrimination test (OHOD) performed in an open-field arena (60 x 60 cm). The circle in the middle of the arena indicates a petri dish containing a paper with odorant covered with fresh bedding. 2-phenylethanol (rose odor) and vanillin were used in habituation and discrimination trials, accordingly. (C) Investigation time (time spent at petri dish, 120 or 240 sec trial duration and 2 min. ITI) of control and HDB silenced mice during odor habituation and discrimination trials (see also Fig. 1 ). (D) Schematic of the stereotaxic injection. (E) Latency (time to reach the petri dish) and investigation time of control and HDB silenced mice during odor habituation and discrimination trials with shorter trial durations. (F) Schematic stereotaxic injection and sequence of experiments. (G) Latency and Investigation time of control and HDB silenced mice during odor habituation and discrimination trials before (blue) and after TeTn virus injection. (H) Schematic of test sequence and stereotaxic injection. (I) Buried food test was conducted in home cage. The ellipse indicates a hidden food pellet. (J) Latency in finding the food pellet of control and HDB silenced mice during buried food test. (K) The puzzle box test paradigm. Left: the arena is divided by black-painted Plexiglas into the start and goal compartments. Right: a timeline of the experiment; the compartments are connected by a door opening (trial 1), open underpass (trials 2-4), underpass blocked by sawdust (trials 5-7), or underpass blocked by a cardboard plug (trials 8-10). (L) Latency (time to enter the goal compartment) of control and HDB silenced mice. 1-way ANOVA followed by Dunnett’s posttest (*) and t-test (#) of sham-injected (n=6) and TeTn-injected (n=6) mice. #, *p

    Article Snippet: 100 µl of a 1:1000 dilution of 2-phenylethanol was utilized for experiments.

    Techniques: Injection, Mouse Assay, Sequencing