pentanol  (Millipore)

 
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  • 95
    Name:
    2 Pentanol
    Description:

    Catalog Number:
    76942
    Price:
    None
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    Structured Review

    Millipore pentanol
    2 Pentanol

    https://www.bioz.com/result/pentanol/product/Millipore
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    pentanol - by Bioz Stars, 2021-05
    95/100 stars

    Images

    1) Product Images from "A Simple Connectivity Scheme for Sparse Coding in an Olfactory System"

    Article Title: A Simple Connectivity Scheme for Sparse Coding in an Olfactory System

    Journal: The Journal of Neuroscience

    doi: 10.1523/JNEUROSCI.4171-06.2007

    Intracellular voltage in single KCs is correlated with local field potentials. A , Reconstruction of the dendritic tree of a KC within the mushroom body calyx (top) and of two PNs (red and green) filled simultaneously within the same antennal lobe (bottom). PN somata and axons lie above and below the plane of glomerular projections. PNs and KC were stained by intracellular injection of Lucifer yellow. B , Simultaneous recording of mushroom body LFP (top, red), KC intracellular voltage (middle, black) and six single-unit PNs (bottom, raster plots) in response to an odor ( cis- 3-hexen-1-ol, horizontal bar indicates odor delivery; top) and at baseline (bottom). Note V m oscillations in response to odor and correlation between Vm and LFP. Calibrations: vertical, 10 mV (V m ), 1 mV (LFP); horizontal, 1 s. C–E , KC membrane potential is highly correlated with the LFP. C , D , Examples of filtered KC V m (KC f ) and LFP recorded simultaneously, and sliding cross-correlograms averaged over nine such trials (bottom). Note frequent covariations of amplitude between KC and LFP in both odor ( C ; pentanol, black bar) and baseline ( D ) conditions. KC f and LFP filtered with the same 5–50 Hz bandpass digital filter. The look-up table represents correlation coefficients: ( C ) −0.4 (blue) to +0.4 (red); ( D ) −0.07 (blue) to +0.07 (red). Calibrations: vertical, 1mV (KCf), 100μV (LFP); horizontal, 1 s. E , Plot of peak correlation coefficients between LFP and V m traces (5 ms time bins) versus time delay for which correlation coefficient is maximal (Δ t max ), for 42 KCs (red triangles) and 22 PNs (blue squares). Each Δ t max is the median over 7–20 trials (pentanol, 512 trials total). KCs and PNs lock to the LFP at different phases; the relevant parameter is the variance of Δ t max , indicating tightness of coupling between single-cell membrane voltage and LFP.
    Figure Legend Snippet: Intracellular voltage in single KCs is correlated with local field potentials. A , Reconstruction of the dendritic tree of a KC within the mushroom body calyx (top) and of two PNs (red and green) filled simultaneously within the same antennal lobe (bottom). PN somata and axons lie above and below the plane of glomerular projections. PNs and KC were stained by intracellular injection of Lucifer yellow. B , Simultaneous recording of mushroom body LFP (top, red), KC intracellular voltage (middle, black) and six single-unit PNs (bottom, raster plots) in response to an odor ( cis- 3-hexen-1-ol, horizontal bar indicates odor delivery; top) and at baseline (bottom). Note V m oscillations in response to odor and correlation between Vm and LFP. Calibrations: vertical, 10 mV (V m ), 1 mV (LFP); horizontal, 1 s. C–E , KC membrane potential is highly correlated with the LFP. C , D , Examples of filtered KC V m (KC f ) and LFP recorded simultaneously, and sliding cross-correlograms averaged over nine such trials (bottom). Note frequent covariations of amplitude between KC and LFP in both odor ( C ; pentanol, black bar) and baseline ( D ) conditions. KC f and LFP filtered with the same 5–50 Hz bandpass digital filter. The look-up table represents correlation coefficients: ( C ) −0.4 (blue) to +0.4 (red); ( D ) −0.07 (blue) to +0.07 (red). Calibrations: vertical, 1mV (KCf), 100μV (LFP); horizontal, 1 s. E , Plot of peak correlation coefficients between LFP and V m traces (5 ms time bins) versus time delay for which correlation coefficient is maximal (Δ t max ), for 42 KCs (red triangles) and 22 PNs (blue squares). Each Δ t max is the median over 7–20 trials (pentanol, 512 trials total). KCs and PNs lock to the LFP at different phases; the relevant parameter is the variance of Δ t max , indicating tightness of coupling between single-cell membrane voltage and LFP.

    Techniques Used: Staining, Injection, Mass Spectrometry

    Related Articles

    other:

    Article Title: Initial Studies Using Aliphatic β-Nitro Alcohols for Therapeutic Corneal Cross-Linking
    Article Snippet: 2-Nitroethanol (2ne), 2-nitro-1-propanol (2nprop), 3-nitro-2-pentanol (3n2pent) [mixture of (±) threo and (±) erythro], dextran T500, NaH2 PO4 , Na2 HPO4 , penicillin (5000 U/mL)/streptomycin (5000 μ g/mL), and ethylenediaminetetraacetic acid (EDTA) were obtained from Sigma Chemical (St. Louis, MO).

    Article Title: Enantioselective Transesterification Catalysis by Nanosized Serine Protease Subtilisin Carlsberg Particles in Tetrahydrofuran
    Article Snippet: Subtilisin Carlsberg (SC), MβCD, 2-butanol ( 1 ), 2-pentanol ( 2 ), 2-hexanol ( 3 ), 2-heptanol ( 4 ), 2-octanol ( 5 ), 3-methyl-2-butanol ( 6 ), 4-methyl-2-pentanol ( 7 ), 5-methyl-2-hexanol ( 8 ), 6-methyl-2-heptanol ( 9 ), 4-phenyl-2-butanol ( 10 ), 4,4-dimethyl-2-pentanol ( 11 ), 4-methyl-4-phenyl-2-pentanol ( 12 ), 1-phenyl-1-propanol ( 13 ), and 1-p-tolyl-1-propanol ( 14 ) were from Sigma-Aldrich (St. Louis, MO).

    Article Title: Comparison of flavour fingerprint, electronic nose and multivariate analysis for discrimination of extra virgin olive oils
    Article Snippet: Chemicals 4-methyl-2-pentanol was purchased from Sigma-Aldrich (St Louis, MO, USA).

    Article Title: Using the Griess colorimetric nitrite assay for measuring aliphatic ?-nitroalcohols
    Article Snippet: 2-nitroethanol (2ne), 2-nitro-1-propanol (2nprop), 3-nitro-2-pentanol (3n2pent), NaH2 PO4 , Na2 HPO4 , sulfanilic acid (SA), N-ethylenediamine hydrochloride (NED), were all obtained from the Sigma-Aldrich Chemical Co (St. Louis, MO).

    Incubation:

    Article Title: In Vitro Bioassay-Guided Identification of Anticancer Properties from Moringa oleifera Lam. Leaf against the MDA-MB-231 Cell Line
    Article Snippet: MDA-MB-231 cells were plated into 24-well plates at the density of 5 × 104 cells/well. .. Cells were incubated with MOL extract (150 µg/mL), fractions no. 1–11 (150 µg/mL), 7-octenoic acid (2.5 and 4 mg/mL), oleamide (70 and 100 μg/mL), 1-phenyl-2-pentanol (600 and 700 μg/mL), or doxorubicin (1.5 μM) for 24 h. Cell apoptosis was examined by staining with Muse™ Annexin V and Dead Cell reagent (EMD Millipore, Billerica, MA, USA; cat. no. MCH100105). ..

    Staining:

    Article Title: In Vitro Bioassay-Guided Identification of Anticancer Properties from Moringa oleifera Lam. Leaf against the MDA-MB-231 Cell Line
    Article Snippet: MDA-MB-231 cells were plated into 24-well plates at the density of 5 × 104 cells/well. .. Cells were incubated with MOL extract (150 µg/mL), fractions no. 1–11 (150 µg/mL), 7-octenoic acid (2.5 and 4 mg/mL), oleamide (70 and 100 μg/mL), 1-phenyl-2-pentanol (600 and 700 μg/mL), or doxorubicin (1.5 μM) for 24 h. Cell apoptosis was examined by staining with Muse™ Annexin V and Dead Cell reagent (EMD Millipore, Billerica, MA, USA; cat. no. MCH100105). ..

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  • 92
    Millipore nb001
    Antitumor effect of MDL-12330A is not linked to inhibition of adenylate cyclase activity. (A) SNU601 and SNU638 cells were exposed to other type of adenylate cyclase inhibitors NKY80 and <t>NB001</t> at indicated concentrations for 24 h, and cell viability was assessed by the EZ-cytox assay. (B) SNU601 and SNU638 cells were incubated with NKY80 or NB001 at 0, 10, 30 and 50 µM for 24 h, and cell lysates were prepared and analyzed by immunoblotting with an antibody to DR5 and BiP.
    Nb001, supplied by Millipore, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nb001/product/Millipore
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    95
    Millipore 4 methyl 4 phenyl 2 pentanol
    Results of the computational modeling of the tetrahedral intermediates of ( R )- (A) and ( S <t>)-4-methyl-4-phenyl-2-pentanol</t> (B). It is apparent that only the S -enantiomer side chain comfortably fits into the substrate binding pocket (residues shown in green).
    4 Methyl 4 Phenyl 2 Pentanol, supplied by Millipore, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/4 methyl 4 phenyl 2 pentanol/product/Millipore
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    4 methyl 4 phenyl 2 pentanol - by Bioz Stars, 2021-05
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    94
    Millipore 1 phenyl 2 entanol
    7-octenoic acid (7-Oct), oleamide (Ole), and <t>1-phenyl-2-pentanol</t> (1-Phe) induced apoptosis and cell cycle arrest in MDA-MB-231 cells. ( A ) Hoechst 33258 staining. ( B , C ) Apoptosis analysis using AnnexinV/7-AAD staining. ( D ) Western blot analysis. ( E , F ) Cycle cell progression. Cells were incubated with 7-octenoic acid (2.5 mg/mL), oleamide (70 µg/mL), 1-phenyl-2-pentanol (600 µg/mL), or doxorubicin (Dox; 1.5 µM) for 24 h in all experiments. Data represent the mean ± SEM of three independent experiments. (* p
    1 Phenyl 2 Entanol, 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/1 phenyl 2 entanol/product/Millipore
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    1 phenyl 2 entanol - by Bioz Stars, 2021-05
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    Image Search Results


    Antitumor effect of MDL-12330A is not linked to inhibition of adenylate cyclase activity. (A) SNU601 and SNU638 cells were exposed to other type of adenylate cyclase inhibitors NKY80 and NB001 at indicated concentrations for 24 h, and cell viability was assessed by the EZ-cytox assay. (B) SNU601 and SNU638 cells were incubated with NKY80 or NB001 at 0, 10, 30 and 50 µM for 24 h, and cell lysates were prepared and analyzed by immunoblotting with an antibody to DR5 and BiP.

    Journal: The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology

    Article Title: MDL-12330A potentiates TRAIL-induced apoptosis in gastric cancer cells through CHOP-mediated DR5 upregulation

    doi: 10.4196/kjpp.2017.21.4.397

    Figure Lengend Snippet: Antitumor effect of MDL-12330A is not linked to inhibition of adenylate cyclase activity. (A) SNU601 and SNU638 cells were exposed to other type of adenylate cyclase inhibitors NKY80 and NB001 at indicated concentrations for 24 h, and cell viability was assessed by the EZ-cytox assay. (B) SNU601 and SNU638 cells were incubated with NKY80 or NB001 at 0, 10, 30 and 50 µM for 24 h, and cell lysates were prepared and analyzed by immunoblotting with an antibody to DR5 and BiP.

    Article Snippet: MDL-12330A, NKY80 and NB001 were purchased from Sigma (MO) and caspase inhibitors were purchased from Calbiochem (CA).

    Techniques: Inhibition, Activity Assay, Incubation

    Repeated ethanol (EtOH) selectively enhanced GluN2B-NMDAR phosphorylation in the DMS in WT, but not AC1KO (KO) mice or mice pretreated with NB001 ( n = 3–5/group). Averaged data (left) and representative immunoblots compiled from groups of images from different parts of the same gel (right) are depicted for DMS (A), DLS (B), or NAc (C) lysates prepared following repeated saline (sal) or EtOH treatment and probed for total and pTyr-1472-GluN2B. (A) A significant increase in pGluN2B levels in the DMS of WT mice was observed following repeated EtOH treatment relative to saline-treated controls, which was absent in AC1KO and NB001 pretreated mice. (B) Repeated ethanol treatment decreased levels of pGluN2B in the DLS equivalently across WT, AC1KO, and NB001-treated mice. (C) No changes in pGluN2B levels in the NAc were observed in response to ethanol or absence of AC1 signaling. Total GluN2B levels were unaffected by AC1 status or ethanol treatment in all three regions. Significance determined by two-way ANOVA and Sidak’s post hoc test, * P

    Journal: The Journal of Pharmacology and Experimental Therapeutics

    Article Title: Adenylyl Cyclase 1 Is Required for Ethanol-Induced Locomotor Sensitization and Associated Increases in NMDA Receptor Phosphorylation and Function in the Dorsal Medial Striatum

    doi: 10.1124/jpet.117.242321

    Figure Lengend Snippet: Repeated ethanol (EtOH) selectively enhanced GluN2B-NMDAR phosphorylation in the DMS in WT, but not AC1KO (KO) mice or mice pretreated with NB001 ( n = 3–5/group). Averaged data (left) and representative immunoblots compiled from groups of images from different parts of the same gel (right) are depicted for DMS (A), DLS (B), or NAc (C) lysates prepared following repeated saline (sal) or EtOH treatment and probed for total and pTyr-1472-GluN2B. (A) A significant increase in pGluN2B levels in the DMS of WT mice was observed following repeated EtOH treatment relative to saline-treated controls, which was absent in AC1KO and NB001 pretreated mice. (B) Repeated ethanol treatment decreased levels of pGluN2B in the DLS equivalently across WT, AC1KO, and NB001-treated mice. (C) No changes in pGluN2B levels in the NAc were observed in response to ethanol or absence of AC1 signaling. Total GluN2B levels were unaffected by AC1 status or ethanol treatment in all three regions. Significance determined by two-way ANOVA and Sidak’s post hoc test, * P

    Article Snippet: Ethanol (200 proof; Fisher Scientific, Waltham, MA) and NB001 (SML0060; Sigma-Aldrich, St. Louis, MO) were diluted in sterile saline for injection to 20% (v/v) and 1 mg/ml solutions, respectively.

    Techniques: Mouse Assay, Western Blot

    Intact acute, but absence of sensitized ethanol (EtOH) locomotor response in AC1KO mice (A–C), n = 6–7/group, and WT mice pretreated with the selective inhibitor NB001 (D–F), 10 mg/kg, n = 8–9/group. Average locomotor activity (A and D) and time course following acute (B and E) or challenge (C and F) EtOH (2.0 g/kg) after repeated home cage EtOH administration (2.5 g/kg, 10 injections). Data reported as percentage change relative to respective saline-only controls. WT EtOH-treated mice displayed an acute locomotor response relative to saline-only WT controls, which was significantly enhanced following sensitization. AC1KO and NB001-treated WT mice demonstrated a comparable acute locomotor response to WT EtOH controls, but failed to display a further potentiation in this response following sensitization. Locomotor activity on the acute and challenge day was unaltered by pretreatment with NB001 alone (NB001 + saline). Significance determined by two-way RM ANOVA and Sidak’s post hoc test, * P ≤ 0.05, compared with respective saline-treated controls; ¥ P

    Journal: The Journal of Pharmacology and Experimental Therapeutics

    Article Title: Adenylyl Cyclase 1 Is Required for Ethanol-Induced Locomotor Sensitization and Associated Increases in NMDA Receptor Phosphorylation and Function in the Dorsal Medial Striatum

    doi: 10.1124/jpet.117.242321

    Figure Lengend Snippet: Intact acute, but absence of sensitized ethanol (EtOH) locomotor response in AC1KO mice (A–C), n = 6–7/group, and WT mice pretreated with the selective inhibitor NB001 (D–F), 10 mg/kg, n = 8–9/group. Average locomotor activity (A and D) and time course following acute (B and E) or challenge (C and F) EtOH (2.0 g/kg) after repeated home cage EtOH administration (2.5 g/kg, 10 injections). Data reported as percentage change relative to respective saline-only controls. WT EtOH-treated mice displayed an acute locomotor response relative to saline-only WT controls, which was significantly enhanced following sensitization. AC1KO and NB001-treated WT mice demonstrated a comparable acute locomotor response to WT EtOH controls, but failed to display a further potentiation in this response following sensitization. Locomotor activity on the acute and challenge day was unaltered by pretreatment with NB001 alone (NB001 + saline). Significance determined by two-way RM ANOVA and Sidak’s post hoc test, * P ≤ 0.05, compared with respective saline-treated controls; ¥ P

    Article Snippet: Ethanol (200 proof; Fisher Scientific, Waltham, MA) and NB001 (SML0060; Sigma-Aldrich, St. Louis, MO) were diluted in sterile saline for injection to 20% (v/v) and 1 mg/ml solutions, respectively.

    Techniques: Mouse Assay, Activity Assay

    Results of the computational modeling of the tetrahedral intermediates of ( R )- (A) and ( S )-4-methyl-4-phenyl-2-pentanol (B). It is apparent that only the S -enantiomer side chain comfortably fits into the substrate binding pocket (residues shown in green).

    Journal: Tetrahedron

    Article Title: Enantioselective Transesterification Catalysis by Nanosized Serine Protease Subtilisin Carlsberg Particles in Tetrahydrofuran

    doi: 10.1016/j.tet.2010.01.053

    Figure Lengend Snippet: Results of the computational modeling of the tetrahedral intermediates of ( R )- (A) and ( S )-4-methyl-4-phenyl-2-pentanol (B). It is apparent that only the S -enantiomer side chain comfortably fits into the substrate binding pocket (residues shown in green).

    Article Snippet: Subtilisin Carlsberg (SC), MβCD, 2-butanol ( 1 ), 2-pentanol ( 2 ), 2-hexanol ( 3 ), 2-heptanol ( 4 ), 2-octanol ( 5 ), 3-methyl-2-butanol ( 6 ), 4-methyl-2-pentanol ( 7 ), 5-methyl-2-hexanol ( 8 ), 6-methyl-2-heptanol ( 9 ), 4-phenyl-2-butanol ( 10 ), 4,4-dimethyl-2-pentanol ( 11 ), 4-methyl-4-phenyl-2-pentanol ( 12 ), 1-phenyl-1-propanol ( 13 ), and 1-p-tolyl-1-propanol ( 14 ) were from Sigma-Aldrich (St. Louis, MO).

    Techniques: Binding Assay

    7-octenoic acid (7-Oct), oleamide (Ole), and 1-phenyl-2-pentanol (1-Phe) induced apoptosis and cell cycle arrest in MDA-MB-231 cells. ( A ) Hoechst 33258 staining. ( B , C ) Apoptosis analysis using AnnexinV/7-AAD staining. ( D ) Western blot analysis. ( E , F ) Cycle cell progression. Cells were incubated with 7-octenoic acid (2.5 mg/mL), oleamide (70 µg/mL), 1-phenyl-2-pentanol (600 µg/mL), or doxorubicin (Dox; 1.5 µM) for 24 h in all experiments. Data represent the mean ± SEM of three independent experiments. (* p

    Journal: Pharmaceuticals

    Article Title: In Vitro Bioassay-Guided Identification of Anticancer Properties from Moringa oleifera Lam. Leaf against the MDA-MB-231 Cell Line

    doi: 10.3390/ph13120464

    Figure Lengend Snippet: 7-octenoic acid (7-Oct), oleamide (Ole), and 1-phenyl-2-pentanol (1-Phe) induced apoptosis and cell cycle arrest in MDA-MB-231 cells. ( A ) Hoechst 33258 staining. ( B , C ) Apoptosis analysis using AnnexinV/7-AAD staining. ( D ) Western blot analysis. ( E , F ) Cycle cell progression. Cells were incubated with 7-octenoic acid (2.5 mg/mL), oleamide (70 µg/mL), 1-phenyl-2-pentanol (600 µg/mL), or doxorubicin (Dox; 1.5 µM) for 24 h in all experiments. Data represent the mean ± SEM of three independent experiments. (* p

    Article Snippet: Oleamide, 7-octenoic acid, and 1-phenyl-2-entanol were from Sigma Aldrich (St. Louis, MO, USA).

    Techniques: Multiple Displacement Amplification, Staining, Western Blot, Incubation

    Effect of 7-octenoic acid, oleamide, and 1-phenyl-2-pentanol in vitro cell migration. ( A ) MDA-MB-231 cells were scratch wounded and incubated with compounds, doxorubicin, or complete medium (control). The wound areas were imaged at 0, 6, 12, and 24 h post-scratching. ( B ) Wound area (%) summarized from triplicate data. One-way ANOVA test was performed with multiple comparison corrections (Dunnett test). Data represent the mean ± SEM of three independent experiments. (* p

    Journal: Pharmaceuticals

    Article Title: In Vitro Bioassay-Guided Identification of Anticancer Properties from Moringa oleifera Lam. Leaf against the MDA-MB-231 Cell Line

    doi: 10.3390/ph13120464

    Figure Lengend Snippet: Effect of 7-octenoic acid, oleamide, and 1-phenyl-2-pentanol in vitro cell migration. ( A ) MDA-MB-231 cells were scratch wounded and incubated with compounds, doxorubicin, or complete medium (control). The wound areas were imaged at 0, 6, 12, and 24 h post-scratching. ( B ) Wound area (%) summarized from triplicate data. One-way ANOVA test was performed with multiple comparison corrections (Dunnett test). Data represent the mean ± SEM of three independent experiments. (* p

    Article Snippet: Oleamide, 7-octenoic acid, and 1-phenyl-2-entanol were from Sigma Aldrich (St. Louis, MO, USA).

    Techniques: In Vitro, Migration, Multiple Displacement Amplification, Incubation