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itraq-based proteomic analysis  (BioTools Co)

 
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    BioTools Co itraq-based proteomic analysis
    Itraq Based Proteomic Analysis, supplied by BioTools Co, 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+proteomic+analysis/itraq+based+proteomic+analysis/pm35109908-96-19-21
    Average 90 stars, based on 1 article reviews
    itraq-based proteomic analysis - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Western Blot:

    Article Title: HDAC6 involves in regulating the lncRNA-microRNA-mRNA network to promote the proliferation of glioblastoma cells.
    Article Snippet: Briefly, 50 pmol desthiobiotin-labeled (PierceTM RNA 3′ End Biotinylation Kit, Thermo Fisher Scientific) androgen receptor (AR) 3′-untranslated regions (UTR) and LINC00461 were captured by 50 μL streptavidin magnetic beads and then interacted with 200 μg lysate extracted from parental and TMZ-resistant Pt#3 cells. .. Elution of RNA-binding protein complexes was applied for western blotting and isobaric tags for relative and absolute quantitation (iTRAQ)-based proteomic analysis (Biotools Co. Ltd., New Taipei City, Taiwan). ..

    Quantitation Assay:

    Article Title: HDAC6 involves in regulating the lncRNA-microRNA-mRNA network to promote the proliferation of glioblastoma cells.
    Article Snippet: Briefly, 50 pmol desthiobiotin-labeled (PierceTM RNA 3′ End Biotinylation Kit, Thermo Fisher Scientific) androgen receptor (AR) 3′-untranslated regions (UTR) and LINC00461 were captured by 50 μL streptavidin magnetic beads and then interacted with 200 μg lysate extracted from parental and TMZ-resistant Pt#3 cells. .. Elution of RNA-binding protein complexes was applied for western blotting and isobaric tags for relative and absolute quantitation (iTRAQ)-based proteomic analysis (Biotools Co. Ltd., New Taipei City, Taiwan). ..

    Multiplex sample analysis:

    Article Title: HDAC6 involves in regulating the lncRNA-microRNA-mRNA network to promote the proliferation of glioblastoma cells.
    Article Snippet: Briefly, 50 pmol desthiobiotin-labeled (PierceTM RNA 3′ End Biotinylation Kit, Thermo Fisher Scientific) androgen receptor (AR) 3′-untranslated regions (UTR) and LINC00461 were captured by 50 μL streptavidin magnetic beads and then interacted with 200 μg lysate extracted from parental and TMZ-resistant Pt#3 cells. .. Elution of RNA-binding protein complexes was applied for western blotting and isobaric tags for relative and absolute quantitation (iTRAQ)-based proteomic analysis (Biotools Co. Ltd., New Taipei City, Taiwan). ..



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    Genechem itraq-based proteomics analysis
    (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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    Image Search Results


    (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