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  • 95
    Millipore afb1
    Afb1, supplied by Millipore, used in various techniques. Bioz Stars score: 95/100, based on 280 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/afb1/product/Millipore
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    92
    Alexis Inc afb1
    Afb1, supplied by Alexis Inc, used in various techniques. Bioz Stars score: 92/100, based on 73 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/afb1/product/Alexis Inc
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    92
    Moravek Biochemicals afb1
    Afb1, supplied by Moravek Biochemicals, used in various techniques. Bioz Stars score: 92/100, based on 45 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/afb1/product/Moravek Biochemicals
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    92
    Supelco afb1
    Afb1, supplied by Supelco, used in various techniques. Bioz Stars score: 92/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/afb1/product/Supelco
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    99
    Millipore afb1 standard
    Aflatoxin production in YEP and YES. Conidia of Aspergillus flavus WT strain were grown in YEP and YES liquid for 7 days, and then 1.5 mL cultures were extracted by chloroform. TLC analysis of extracts from both YES and YEP, along with an <t>AFB1</t> standard.
    Afb1 Standard, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 73 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    afb1  (Lpath)
    92
    Lpath afb1
    Aflatoxin production in YEP and YES. Conidia of Aspergillus flavus WT strain were grown in YEP and YES liquid for 7 days, and then 1.5 mL cultures were extracted by chloroform. TLC analysis of extracts from both YES and YEP, along with an <t>AFB1</t> standard.
    Afb1, supplied by Lpath, used in various techniques. Bioz Stars score: 92/100, based on 32 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/afb1/product/Lpath
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    92
    Nanoprobes afb1
    Aflatoxin production in YEP and YES. Conidia of Aspergillus flavus WT strain were grown in YEP and YES liquid for 7 days, and then 1.5 mL cultures were extracted by chloroform. TLC analysis of extracts from both YES and YEP, along with an <t>AFB1</t> standard.
    Afb1, supplied by Nanoprobes, used in various techniques. Bioz Stars score: 92/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/afb1/product/Nanoprobes
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    94
    Cayman Chemical afb1
    Expression of caspase-3 protein in chicken hepatocytes. The cells were pre-treated for 24 h with different concentrations of PEF ranging from 0 to 40 μg/ml and positive control (gallic acid, 10 μM or 1.7 μg/ml). The media were replaced with a medium containing 5 μM of <t>AFB1</t> and the cells incubated for another 48 h. All values represent mean ± standard error from three independent experiments. *** p
    Afb1, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/afb1/product/Cayman Chemical
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    88
    Schiff Nutrition International afb1 dialdehyde
    Expression of caspase-3 protein in chicken hepatocytes. The cells were pre-treated for 24 h with different concentrations of PEF ranging from 0 to 40 μg/ml and positive control (gallic acid, 10 μM or 1.7 μg/ml). The media were replaced with a medium containing 5 μM of <t>AFB1</t> and the cells incubated for another 48 h. All values represent mean ± standard error from three independent experiments. *** p
    Afb1 Dialdehyde, supplied by Schiff Nutrition International, used in various techniques. Bioz Stars score: 88/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Mine Safety Appliances afb1
    The effects of <t>AFB1</t> (5 mM), MSA (10 μg/mL) and different concentrations of MSA (5, 10, 20 and 40 mg/mL) together with AFBı on the number of SCEs and MN in human peripheral lymphocytes. All data are shown as mean ± SE. Statistically significant differences (One-way ANOVA with Dunnett’s multiple comparison test) are as follows; p > 0.05 (not significant, ns), * p
    Afb1, supplied by Mine Safety Appliances, used in various techniques. Bioz Stars score: 91/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Neogen iac afb1
    Comparison of recovery rates for the MNP-mAb conjugates <t>(fMA-AFB1</t> and fMA-ZEN) and immunoaffinity columns <t>(IAC-AFB1</t> and IAC-ZEN) from corn (A) or product X (B) feed samples (n = 3). Recovery rate (%) = (amount of purified mycotoxins/amount of spiked mycotoxins) × 100. * p
    Iac Afb1, supplied by Neogen, 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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    afb1  (Vicam)
    92
    Vicam afb1
    HPLC chromatograms of a: Blank rice sample, b: <t>AFB1</t> standard (3.6 ng/mL) and c: Contaminated puffed corn snack (5 ng/g).
    Afb1, supplied by Vicam, used in various techniques. Bioz Stars score: 92/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Biopure Corporation c17 afb1
    HPLC chromatograms of a: Blank rice sample, b: <t>AFB1</t> standard (3.6 ng/mL) and c: Contaminated puffed corn snack (5 ng/g).
    C17 Afb1, supplied by Biopure Corporation, used in various techniques. Bioz Stars score: 94/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Toronto Research Chemicals afb1 n7 guanine standard
    HPLC chromatograms of a: Blank rice sample, b: <t>AFB1</t> standard (3.6 ng/mL) and c: Contaminated puffed corn snack (5 ng/g).
    Afb1 N7 Guanine Standard, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 92/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Millipore afb1 standard solution
    HPLC chromatograms of a: Blank rice sample, b: <t>AFB1</t> standard (3.6 ng/mL) and c: Contaminated puffed corn snack (5 ng/g).
    Afb1 Standard Solution, supplied by Millipore, used in various techniques. Bioz Stars score: 94/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Millipore aflatoxins afb1
    HPLC chromatograms of a: Blank rice sample, b: <t>AFB1</t> standard (3.6 ng/mL) and c: Contaminated puffed corn snack (5 ng/g).
    Aflatoxins Afb1, supplied by Millipore, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Aflatoxin production in YEP and YES. Conidia of Aspergillus flavus WT strain were grown in YEP and YES liquid for 7 days, and then 1.5 mL cultures were extracted by chloroform. TLC analysis of extracts from both YES and YEP, along with an AFB1 standard.

    Journal: Frontiers in Microbiology

    Article Title: Exploration of the Regulatory Mechanism of Secondary Metabolism by Comparative Transcriptomics in Aspergillus flavus

    doi: 10.3389/fmicb.2018.01568

    Figure Lengend Snippet: Aflatoxin production in YEP and YES. Conidia of Aspergillus flavus WT strain were grown in YEP and YES liquid for 7 days, and then 1.5 mL cultures were extracted by chloroform. TLC analysis of extracts from both YES and YEP, along with an AFB1 standard.

    Article Snippet: The AFB1 concentration of each sample was counted by using a calibration curves and the AFB1 standard (HPLC grade) were purchased from Sigma (Sigma, Germany).

    Techniques: Thin Layer Chromatography

    Frequency shifting associated with the amount of the surface-bound AFB1-BSA recorded in PBS solution (pH = 7.5) with the LW-SAW sensor.

    Journal: Sensors (Basel, Switzerland)

    Article Title: Enhanced Sensitive Love Wave Surface Acoustic Wave Sensor Designed for Immunoassay Formats

    doi: 10.3390/s150510511

    Figure Lengend Snippet: Frequency shifting associated with the amount of the surface-bound AFB1-BSA recorded in PBS solution (pH = 7.5) with the LW-SAW sensor.

    Article Snippet: Materials 11-mercaptoundecanoic acid (11-MUA) and 1-ethyl-3-(3-dimethylaminopropyl carbodiimide) hydrochloride (EDC), bovine serum albumin (BSA), hydrochloric acid and AFB1-BSA bioconjugate were purchased from Sigma–Aldrich.

    Techniques:

    PCA and Multivariate data analysis of AFB1 by different Actinomycete strains at variable time frames.

    Journal: Toxins

    Article Title: Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    doi: 10.3390/toxins7020439

    Figure Lengend Snippet: PCA and Multivariate data analysis of AFB1 by different Actinomycete strains at variable time frames.

    Article Snippet: AFB1 Degradation by Actinomycetes in Liquid Culture 0.2 mL of a 100 µg/mL AFB1 dissolved in methanol (Sigma Aldrich, Dorset, UK.) was added to 2 mL Eppendorf tubes.

    Techniques:

    Chemical structure for AFB1.

    Journal: Toxins

    Article Title: Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    doi: 10.3390/toxins7020439

    Figure Lengend Snippet: Chemical structure for AFB1.

    Article Snippet: AFB1 Degradation by Actinomycetes in Liquid Culture 0.2 mL of a 100 µg/mL AFB1 dissolved in methanol (Sigma Aldrich, Dorset, UK.) was added to 2 mL Eppendorf tubes.

    Techniques:

    The effect of incubation temperature on AFB1 degradation over the first 24 h of culture at pH 6.0. The values are the mean of three replicates and their standard errors. Means with different letters are significantly different according to the Bonferroni Multiple Comparisons Test ( p

    Journal: Toxins

    Article Title: Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    doi: 10.3390/toxins7020439

    Figure Lengend Snippet: The effect of incubation temperature on AFB1 degradation over the first 24 h of culture at pH 6.0. The values are the mean of three replicates and their standard errors. Means with different letters are significantly different according to the Bonferroni Multiple Comparisons Test ( p

    Article Snippet: AFB1 Degradation by Actinomycetes in Liquid Culture 0.2 mL of a 100 µg/mL AFB1 dissolved in methanol (Sigma Aldrich, Dorset, UK.) was added to 2 mL Eppendorf tubes.

    Techniques: Incubation

    PCA analysis of AFB1 degradation by different Actinomycete strains showing the marker metabolites.

    Journal: Toxins

    Article Title: Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    doi: 10.3390/toxins7020439

    Figure Lengend Snippet: PCA analysis of AFB1 degradation by different Actinomycete strains showing the marker metabolites.

    Article Snippet: AFB1 Degradation by Actinomycetes in Liquid Culture 0.2 mL of a 100 µg/mL AFB1 dissolved in methanol (Sigma Aldrich, Dorset, UK.) was added to 2 mL Eppendorf tubes.

    Techniques: Marker

    The effect of culture pH on AFB1 degradation at 30 °C over the first 24 h of incubation. Means with different letters are significantly different according to the Bonferroni Multiple Comparisons Test ( p

    Journal: Toxins

    Article Title: Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    doi: 10.3390/toxins7020439

    Figure Lengend Snippet: The effect of culture pH on AFB1 degradation at 30 °C over the first 24 h of incubation. Means with different letters are significantly different according to the Bonferroni Multiple Comparisons Test ( p

    Article Snippet: AFB1 Degradation by Actinomycetes in Liquid Culture 0.2 mL of a 100 µg/mL AFB1 dissolved in methanol (Sigma Aldrich, Dorset, UK.) was added to 2 mL Eppendorf tubes.

    Techniques: Incubation

    Hypothetical degradation mechanism for AFB1 by R. erythropolis .

    Journal: Toxins

    Article Title: Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    doi: 10.3390/toxins7020439

    Figure Lengend Snippet: Hypothetical degradation mechanism for AFB1 by R. erythropolis .

    Article Snippet: AFB1 Degradation by Actinomycetes in Liquid Culture 0.2 mL of a 100 µg/mL AFB1 dissolved in methanol (Sigma Aldrich, Dorset, UK.) was added to 2 mL Eppendorf tubes.

    Techniques:

    Kinetics of degradation of AFB1 over the first 16 h of incubation at pH 6.

    Journal: Toxins

    Article Title: Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    doi: 10.3390/toxins7020439

    Figure Lengend Snippet: Kinetics of degradation of AFB1 over the first 16 h of incubation at pH 6.

    Article Snippet: AFB1 Degradation by Actinomycetes in Liquid Culture 0.2 mL of a 100 µg/mL AFB1 dissolved in methanol (Sigma Aldrich, Dorset, UK.) was added to 2 mL Eppendorf tubes.

    Techniques: Incubation

    AFB1 degradation by cultures of R. erythropolis ATCC 4277 , S. lividans TK 24 and S. aureofaciens ATCC10762 after 24 h incubation at 30 °C and pH 6.0.

    Journal: Toxins

    Article Title: Metabolomics of the Bio-Degradation Process of Aflatoxin B1 by Actinomycetes at an Initial pH of 6.0

    doi: 10.3390/toxins7020439

    Figure Lengend Snippet: AFB1 degradation by cultures of R. erythropolis ATCC 4277 , S. lividans TK 24 and S. aureofaciens ATCC10762 after 24 h incubation at 30 °C and pH 6.0.

    Article Snippet: AFB1 Degradation by Actinomycetes in Liquid Culture 0.2 mL of a 100 µg/mL AFB1 dissolved in methanol (Sigma Aldrich, Dorset, UK.) was added to 2 mL Eppendorf tubes.

    Techniques: Incubation

    Expression of caspase-3 protein in chicken hepatocytes. The cells were pre-treated for 24 h with different concentrations of PEF ranging from 0 to 40 μg/ml and positive control (gallic acid, 10 μM or 1.7 μg/ml). The media were replaced with a medium containing 5 μM of AFB1 and the cells incubated for another 48 h. All values represent mean ± standard error from three independent experiments. *** p

    Journal: BMC Complementary and Alternative Medicine

    Article Title: Cytoprotective effect of palm kernel cake phenolics against aflatoxin B1-induced cell damage and its underlying mechanism of action

    doi: 10.1186/s12906-015-0921-z

    Figure Lengend Snippet: Expression of caspase-3 protein in chicken hepatocytes. The cells were pre-treated for 24 h with different concentrations of PEF ranging from 0 to 40 μg/ml and positive control (gallic acid, 10 μM or 1.7 μg/ml). The media were replaced with a medium containing 5 μM of AFB1 and the cells incubated for another 48 h. All values represent mean ± standard error from three independent experiments. *** p

    Article Snippet: The cells were incubated for 24 h, and then the media were replaced with the fresh media containing 5 μM of AFB1 (Cayman Chemical Company, Ann Arbor, MI, USA) and incubated for another 48 h. Finally, the viability of the cells was determined by using 3–(4,5–Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay.

    Techniques: Expressing, Positive Control, Incubation

    This diagram illustrates the probable protective mechanisms of PEF in chicken hepatocytes exposed to AFB1

    Journal: BMC Complementary and Alternative Medicine

    Article Title: Cytoprotective effect of palm kernel cake phenolics against aflatoxin B1-induced cell damage and its underlying mechanism of action

    doi: 10.1186/s12906-015-0921-z

    Figure Lengend Snippet: This diagram illustrates the probable protective mechanisms of PEF in chicken hepatocytes exposed to AFB1

    Article Snippet: The cells were incubated for 24 h, and then the media were replaced with the fresh media containing 5 μM of AFB1 (Cayman Chemical Company, Ann Arbor, MI, USA) and incubated for another 48 h. Finally, the viability of the cells was determined by using 3–(4,5–Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay.

    Techniques:

    Flow cytometry analyses of chicken hepatocytes pretreated with phenolic-enriched fraction (PEF) and exposed to 5 μM of AFB1. The a, b, c, d and e showed cells pretreated with 0, 5, 10, 20 and 40 μg/ml of PEF, respectively. The f indicated that the cells were pretreated with gallic acid at the concentration of 10 μM or 1.7 μg/ml

    Journal: BMC Complementary and Alternative Medicine

    Article Title: Cytoprotective effect of palm kernel cake phenolics against aflatoxin B1-induced cell damage and its underlying mechanism of action

    doi: 10.1186/s12906-015-0921-z

    Figure Lengend Snippet: Flow cytometry analyses of chicken hepatocytes pretreated with phenolic-enriched fraction (PEF) and exposed to 5 μM of AFB1. The a, b, c, d and e showed cells pretreated with 0, 5, 10, 20 and 40 μg/ml of PEF, respectively. The f indicated that the cells were pretreated with gallic acid at the concentration of 10 μM or 1.7 μg/ml

    Article Snippet: The cells were incubated for 24 h, and then the media were replaced with the fresh media containing 5 μM of AFB1 (Cayman Chemical Company, Ann Arbor, MI, USA) and incubated for another 48 h. Finally, the viability of the cells was determined by using 3–(4,5–Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay.

    Techniques: Flow Cytometry, Cytometry, Concentration Assay

    This diagram illustrates the events taking place in un-treated chicken hepatocytes exposed to AFB1

    Journal: BMC Complementary and Alternative Medicine

    Article Title: Cytoprotective effect of palm kernel cake phenolics against aflatoxin B1-induced cell damage and its underlying mechanism of action

    doi: 10.1186/s12906-015-0921-z

    Figure Lengend Snippet: This diagram illustrates the events taking place in un-treated chicken hepatocytes exposed to AFB1

    Article Snippet: The cells were incubated for 24 h, and then the media were replaced with the fresh media containing 5 μM of AFB1 (Cayman Chemical Company, Ann Arbor, MI, USA) and incubated for another 48 h. Finally, the viability of the cells was determined by using 3–(4,5–Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay.

    Techniques:

    The cytoprotective activity of PEF and gallic acid against AFB1-cell damage. All values are means ± S.E.M of three independent experiments. The cells were pre-treated with different concentrations of PEF and gallic acid as positive control (10 μM or 1.7 μg/ml) for 24 h and then the media were replaced with a medium containing 5 μM of AFB1 and the cells were incubated for another 48 h. The experiment was performed in triplicate. *** p

    Journal: BMC Complementary and Alternative Medicine

    Article Title: Cytoprotective effect of palm kernel cake phenolics against aflatoxin B1-induced cell damage and its underlying mechanism of action

    doi: 10.1186/s12906-015-0921-z

    Figure Lengend Snippet: The cytoprotective activity of PEF and gallic acid against AFB1-cell damage. All values are means ± S.E.M of three independent experiments. The cells were pre-treated with different concentrations of PEF and gallic acid as positive control (10 μM or 1.7 μg/ml) for 24 h and then the media were replaced with a medium containing 5 μM of AFB1 and the cells were incubated for another 48 h. The experiment was performed in triplicate. *** p

    Article Snippet: The cells were incubated for 24 h, and then the media were replaced with the fresh media containing 5 μM of AFB1 (Cayman Chemical Company, Ann Arbor, MI, USA) and incubated for another 48 h. Finally, the viability of the cells was determined by using 3–(4,5–Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay.

    Techniques: Activity Assay, Positive Control, Incubation

    Expression of nrf2 protein in chicken hepatocytes. The cells were pre-treated for 24 h with different concentrations of PEF ranging from 0 to 40 μg/ml and positive control (gallic acid, 10 μM or 1.7 μg/ml). The media were replaced with a medium containing 5 μM of AFB1 and the cells were incubated for another 48 h. All values represent means ± SEM from three independent experiments. *** p

    Journal: BMC Complementary and Alternative Medicine

    Article Title: Cytoprotective effect of palm kernel cake phenolics against aflatoxin B1-induced cell damage and its underlying mechanism of action

    doi: 10.1186/s12906-015-0921-z

    Figure Lengend Snippet: Expression of nrf2 protein in chicken hepatocytes. The cells were pre-treated for 24 h with different concentrations of PEF ranging from 0 to 40 μg/ml and positive control (gallic acid, 10 μM or 1.7 μg/ml). The media were replaced with a medium containing 5 μM of AFB1 and the cells were incubated for another 48 h. All values represent means ± SEM from three independent experiments. *** p

    Article Snippet: The cells were incubated for 24 h, and then the media were replaced with the fresh media containing 5 μM of AFB1 (Cayman Chemical Company, Ann Arbor, MI, USA) and incubated for another 48 h. Finally, the viability of the cells was determined by using 3–(4,5–Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay.

    Techniques: Expressing, Positive Control, Incubation

    Expression of Hsp70 protein in chicken hepatocytes. The cells were pre-treated for 24 h with different concentrations of PEF ranging from 0 to 40 μg/ml and positive control (gallic acid, 10 μM or 1.7 μg/ml). The media were replaced with a medium containing 5 μM of AFB1 and the cells were incubated for another 48 h. All values represent means ± SEM from three independent experiments. *** p

    Journal: BMC Complementary and Alternative Medicine

    Article Title: Cytoprotective effect of palm kernel cake phenolics against aflatoxin B1-induced cell damage and its underlying mechanism of action

    doi: 10.1186/s12906-015-0921-z

    Figure Lengend Snippet: Expression of Hsp70 protein in chicken hepatocytes. The cells were pre-treated for 24 h with different concentrations of PEF ranging from 0 to 40 μg/ml and positive control (gallic acid, 10 μM or 1.7 μg/ml). The media were replaced with a medium containing 5 μM of AFB1 and the cells were incubated for another 48 h. All values represent means ± SEM from three independent experiments. *** p

    Article Snippet: The cells were incubated for 24 h, and then the media were replaced with the fresh media containing 5 μM of AFB1 (Cayman Chemical Company, Ann Arbor, MI, USA) and incubated for another 48 h. Finally, the viability of the cells was determined by using 3–(4,5–Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay.

    Techniques: Expressing, Positive Control, Incubation

    The effects of AFB1 (5 mM), MSA (10 μg/mL) and different concentrations of MSA (5, 10, 20 and 40 mg/mL) together with AFBı on the number of SCEs and MN in human peripheral lymphocytes. All data are shown as mean ± SE. Statistically significant differences (One-way ANOVA with Dunnett’s multiple comparison test) are as follows; p > 0.05 (not significant, ns), * p

    Journal: Cytotechnology

    Article Title: Antioxidant and antigenotoxic potencies of Sempervivum armenum on human lymphocytes in vitro

    doi: 10.1007/s10616-016-0030-y

    Figure Lengend Snippet: The effects of AFB1 (5 mM), MSA (10 μg/mL) and different concentrations of MSA (5, 10, 20 and 40 mg/mL) together with AFBı on the number of SCEs and MN in human peripheral lymphocytes. All data are shown as mean ± SE. Statistically significant differences (One-way ANOVA with Dunnett’s multiple comparison test) are as follows; p > 0.05 (not significant, ns), * p

    Article Snippet: The experiments were conducted in seven groups as follows: Group 1: Control, Group 2: AFB1 (5 µM), Group 3: MSA (10 mg/mL), Group 4: AFB1 (5 µM) + MSA (5 mg/mL), Group 5: AFB1 (5 µM) + MSA (10 mg/mL), Group 6: AFB1 (5 µM) + MSA (20 mg/mL), Group 7: AFB1 (5 µM) + MSA (40 mg/mL).

    Techniques:

    Comparison of recovery rates for the MNP-mAb conjugates (fMA-AFB1 and fMA-ZEN) and immunoaffinity columns (IAC-AFB1 and IAC-ZEN) from corn (A) or product X (B) feed samples (n = 3). Recovery rate (%) = (amount of purified mycotoxins/amount of spiked mycotoxins) × 100. * p

    Journal: Journal of Veterinary Science

    Article Title: A novel mycotoxin purification system using magnetic nanoparticles for the recovery of aflatoxin B1 and zearalenone from feed

    doi: 10.4142/jvs.2012.13.4.363

    Figure Lengend Snippet: Comparison of recovery rates for the MNP-mAb conjugates (fMA-AFB1 and fMA-ZEN) and immunoaffinity columns (IAC-AFB1 and IAC-ZEN) from corn (A) or product X (B) feed samples (n = 3). Recovery rate (%) = (amount of purified mycotoxins/amount of spiked mycotoxins) × 100. * p

    Article Snippet: IAC-AFB1 (NeoColumn; Neogen, USA) and IAC-ZEN (Easi-extract zearalenone; R-Biopharm, Germany) were used to isolate AFB1 and ZEN, respectively, and the mycotoxins were purified following the manufacturer's protocol.

    Techniques: Purification

    HPLC chromatograms of a: Blank rice sample, b: AFB1 standard (3.6 ng/mL) and c: Contaminated puffed corn snack (5 ng/g).

    Journal: Iranian Journal of Pharmaceutical Research : IJPR

    Article Title: Analysis of Aflatoxin B1 in Iranian Foods Using HPLC and a Monolithic Column and Estimation of its Dietary Intake

    doi:

    Figure Lengend Snippet: HPLC chromatograms of a: Blank rice sample, b: AFB1 standard (3.6 ng/mL) and c: Contaminated puffed corn snack (5 ng/g).

    Article Snippet: The IAC for AFB1 was purchased from Vicam Company, MA, USA.

    Techniques: High Performance Liquid Chromatography