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itraq-based quantitative proteomics analysis  (Dawley Inc)

 
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    Dawley Inc itraq-based quantitative proteomics analysis
    Itraq Based Quantitative Proteomics Analysis, supplied by Dawley Inc, 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/product/itraq-based+proteomics+analysis/itraq+based+quantitative+proteomics+analysis/pm39181731-242-7-10
    Average 90 stars, based on 1 article reviews
    itraq-based quantitative proteomics analysis - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Multiplex sample analysis:

    Article Title: Per- and polyfluoroalkyl substances as persistent pollutants with metabolic and endocrine-disrupting impacts.
    Article Snippet: PFASs have been found to disrupt The widespread use of perand polyfluoroalkyl substances (PFASs), and their resistance to degradation, renders human exposure to them inevitable.. PFAS exposure disturbs endocrine function, potentially affecting cognitive development in newborns through thyroid dysfunction during pregnancy.. Recent studies reveal varyingmale and female reproductive toxicity across PFASclasses,with alternative analogs affecting sperm parameters and legacy PFASs correlating with conditions like endometriosis.

    Quantitative Proteomics:

    Article Title: Per- and polyfluoroalkyl substances as persistent pollutants with metabolic and endocrine-disrupting impacts.
    Article Snippet: PFASs have been found to disrupt The widespread use of perand polyfluoroalkyl substances (PFASs), and their resistance to degradation, renders human exposure to them inevitable.. PFAS exposure disturbs endocrine function, potentially affecting cognitive development in newborns through thyroid dysfunction during pregnancy.. Recent studies reveal varyingmale and female reproductive toxicity across PFASclasses,with alternative analogs affecting sperm parameters and legacy PFASs correlating with conditions like endometriosis.



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    (A,B) iTRAQ-based <t>proteomics</t> analysis. (A) Apoptosis promotors Casp9 , Casp8 , Bak1, and Dap were significantly down-regulated by YKL-40, while the apoptosis inhibitor Aven was significantly up-regulated. (B) Volcano Plot . Molecules down-regulated by YKL-40 are presented in the upper left area (green down arrow) while those up-regulated are shown in the upper right area (red up arrow), and those involved in apoptosis regulation are marked with up/down solid arrows. The most significant fold change ( FC ) on the expression level of these molecules was caused by Casp9 ( FC = 0.6411), followed by Aven ( FC = 1.3006). (C,D) Caspase-9 expression levels detected in BMDM and aorta tissues of Ldlr −/- mice. YKL-40 significantly down-regulated the activation level of caspase-9. (E) In RAW264.7, which was upregulated by Ykl-40 , the activation level of caspase-9 was significantly lower than that in control group ( p = 0.0054) while the expression level of Aven was significantly higher than in controls ( p = 0.0031). There was no significant difference in caspase-9 activation and Aven expression level between the Ykl40 downregulated group and normal controls ( p > 0.05). (F) Genetic expression relative fold changes of Casp9 , Dap , Aven and Bak1. No significant difference was indicated on Casp9 in BMDM after being treated by YKL-40 recombinant protein, but Aven was significantly up-regulated. (G) Casp9 , Aven expression levels were significantly upregulated in Ykl40 upregulated RAW264.7 ( p = 0.0154, p < 0.0001) and downregulated in the Ykl40 downregulated group ( p = 0.0039, p = 0.0037).
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    (A,B) iTRAQ-based proteomics analysis. (A) Apoptosis promotors Casp9 , Casp8 , Bak1, and Dap were significantly down-regulated by YKL-40, while the apoptosis inhibitor Aven was significantly up-regulated. (B) Volcano Plot . Molecules down-regulated by YKL-40 are presented in the upper left area (green down arrow) while those up-regulated are shown in the upper right area (red up arrow), and those involved in apoptosis regulation are marked with up/down solid arrows. The most significant fold change ( FC ) on the expression level of these molecules was caused by Casp9 ( FC = 0.6411), followed by Aven ( FC = 1.3006). (C,D) Caspase-9 expression levels detected in BMDM and aorta tissues of Ldlr −/- mice. YKL-40 significantly down-regulated the activation level of caspase-9. (E) In RAW264.7, which was upregulated by Ykl-40 , the activation level of caspase-9 was significantly lower than that in control group ( p = 0.0054) while the expression level of Aven was significantly higher than in controls ( p = 0.0031). There was no significant difference in caspase-9 activation and Aven expression level between the Ykl40 downregulated group and normal controls ( p > 0.05). (F) Genetic expression relative fold changes of Casp9 , Dap , Aven and Bak1. No significant difference was indicated on Casp9 in BMDM after being treated by YKL-40 recombinant protein, but Aven was significantly up-regulated. (G) Casp9 , Aven expression levels were significantly upregulated in Ykl40 upregulated RAW264.7 ( p = 0.0154, p < 0.0001) and downregulated in the Ykl40 downregulated group ( p = 0.0039, p = 0.0037).

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: YKL-40 Aggravates Early-Stage Atherosclerosis by Inhibiting Macrophage Apoptosis in an Aven-dependent Way

    doi: 10.3389/fcell.2021.752773

    Figure Lengend Snippet: (A,B) iTRAQ-based proteomics analysis. (A) Apoptosis promotors Casp9 , Casp8 , Bak1, and Dap were significantly down-regulated by YKL-40, while the apoptosis inhibitor Aven was significantly up-regulated. (B) Volcano Plot . Molecules down-regulated by YKL-40 are presented in the upper left area (green down arrow) while those up-regulated are shown in the upper right area (red up arrow), and those involved in apoptosis regulation are marked with up/down solid arrows. The most significant fold change ( FC ) on the expression level of these molecules was caused by Casp9 ( FC = 0.6411), followed by Aven ( FC = 1.3006). (C,D) Caspase-9 expression levels detected in BMDM and aorta tissues of Ldlr −/- mice. YKL-40 significantly down-regulated the activation level of caspase-9. (E) In RAW264.7, which was upregulated by Ykl-40 , the activation level of caspase-9 was significantly lower than that in control group ( p = 0.0054) while the expression level of Aven was significantly higher than in controls ( p = 0.0031). There was no significant difference in caspase-9 activation and Aven expression level between the Ykl40 downregulated group and normal controls ( p > 0.05). (F) Genetic expression relative fold changes of Casp9 , Dap , Aven and Bak1. No significant difference was indicated on Casp9 in BMDM after being treated by YKL-40 recombinant protein, but Aven was significantly up-regulated. (G) Casp9 , Aven expression levels were significantly upregulated in Ykl40 upregulated RAW264.7 ( p = 0.0154, p < 0.0001) and downregulated in the Ykl40 downregulated group ( p = 0.0039, p = 0.0037).

    Article Snippet: iTRAQ-based proteomics analysis (Genechem Co.,Ltd., Shanghai, China) were performed to screen out the potential downstream target molecules of YKL-40.

    Techniques: Expressing, Activation Assay, Recombinant