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  • 92
    ATCC s heerlen atcc 15792
    S Heerlen Atcc 15792, supplied by ATCC, 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/s heerlen atcc 15792/product/ATCC
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    s heerlen atcc 15792 - by Bioz Stars, 2024-02
    92/100 stars
      Buy from Supplier

    93
    Proteintech s100a8
    Confocal microscopy (lung, liver, spleen, brain) of PKH67-labeled Panc02 EXO and Panc02-H7 EXO tissue distribution (green) 24 hpi. (A) PKH-67-labeled liposomes served as controls (scale bar=100 μm). Histogram shows exosome tissue distribution quantification (n=5/group). CD45, p-Stat3, and CD11b IF staining in liver sections from controls (left) and mice treated with Panc02 EXOs(middle) or Panc02-H7 EXOs (right) for 12 d without tumor challenge. (B) Histogram shows infiltrating CD45 + cell quantification. FN and α-SMA IF staining in liver sections from controls (top) and mice treated with Panc02 EXOs(middle) or Panc02-H7 EXOs (bottom) for 12 d without tumor challenge. (C) Histogram shows infiltrating α-SMA + hStCs and FN expression quantification(400× magnification; n=5/group). Western blotting analysis showed upregulated <t>S100A8</t> and S100A9 in livers treated with Panc02-H7-derived exosomes. Histogram shows expression of the three proteins in three groupsas determined by densitometric analysis (n=3/group). (D) Pancreatic cancer-derived exosomes induce MDSC accumulation in peripheral blood. (E) Representative flow cytometric plots (left) and quantification (right) of CD11b + GR1 + MDSCs (n=5/group). *P<0.05, **P<0.01,***P<0.001.
    S100a8, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/s100a8/product/Proteintech
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    s100a8 - by Bioz Stars, 2024-02
    93/100 stars
      Buy from Supplier

    93
    Proteintech mouse anti s100a8 antibody
    PPI network and the significant module of DEGs. (A) The PPI network of DEGs. (B) The significant module was obtained from PPI network constructed using Cytoscape with 13 nodes and 57 edges. <t>S100A8</t> is marked in yellow, and downregulated genes are marked in green.
    Mouse Anti S100a8 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti s100a8 antibody/product/Proteintech
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mouse anti s100a8 antibody - by Bioz Stars, 2024-02
    93/100 stars
      Buy from Supplier

    93
    Proteintech anti kdm3a
    Sequential recruitment of histone modifying enzymes by BRG1. (A–D) EAhy926 cells were transfected with siRNA targeting BRG1 or scrambled siRNA (SCR) followed by treatment with Ang II (1 μM). Cells were harvested at indicated time points and ChIP assays were performed with anti-acetyl H3 (A) , anti-dimethyl H3K9 (B) , anti-p300 (C) , or <t>anti-KDM3A</t> (D) . All experiments were repeated three times and one representative experiment is shown. Error bars represent SD (* p < 0.05, one-way ANOVA with post hoc Scheffe test).
    Anti Kdm3a, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti kdm3a/product/Proteintech
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti kdm3a - by Bioz Stars, 2024-02
    93/100 stars
      Buy from Supplier

    Image Search Results


    Confocal microscopy (lung, liver, spleen, brain) of PKH67-labeled Panc02 EXO and Panc02-H7 EXO tissue distribution (green) 24 hpi. (A) PKH-67-labeled liposomes served as controls (scale bar=100 μm). Histogram shows exosome tissue distribution quantification (n=5/group). CD45, p-Stat3, and CD11b IF staining in liver sections from controls (left) and mice treated with Panc02 EXOs(middle) or Panc02-H7 EXOs (right) for 12 d without tumor challenge. (B) Histogram shows infiltrating CD45 + cell quantification. FN and α-SMA IF staining in liver sections from controls (top) and mice treated with Panc02 EXOs(middle) or Panc02-H7 EXOs (bottom) for 12 d without tumor challenge. (C) Histogram shows infiltrating α-SMA + hStCs and FN expression quantification(400× magnification; n=5/group). Western blotting analysis showed upregulated S100A8 and S100A9 in livers treated with Panc02-H7-derived exosomes. Histogram shows expression of the three proteins in three groupsas determined by densitometric analysis (n=3/group). (D) Pancreatic cancer-derived exosomes induce MDSC accumulation in peripheral blood. (E) Representative flow cytometric plots (left) and quantification (right) of CD11b + GR1 + MDSCs (n=5/group). *P<0.05, **P<0.01,***P<0.001.

    Journal: Oncotarget

    Article Title: Pancreatic cancer-derived exosomes promote tumor metastasis and liver pre-metastatic niche formation

    doi: 10.18632/oncotarget.18831

    Figure Lengend Snippet: Confocal microscopy (lung, liver, spleen, brain) of PKH67-labeled Panc02 EXO and Panc02-H7 EXO tissue distribution (green) 24 hpi. (A) PKH-67-labeled liposomes served as controls (scale bar=100 μm). Histogram shows exosome tissue distribution quantification (n=5/group). CD45, p-Stat3, and CD11b IF staining in liver sections from controls (left) and mice treated with Panc02 EXOs(middle) or Panc02-H7 EXOs (right) for 12 d without tumor challenge. (B) Histogram shows infiltrating CD45 + cell quantification. FN and α-SMA IF staining in liver sections from controls (top) and mice treated with Panc02 EXOs(middle) or Panc02-H7 EXOs (bottom) for 12 d without tumor challenge. (C) Histogram shows infiltrating α-SMA + hStCs and FN expression quantification(400× magnification; n=5/group). Western blotting analysis showed upregulated S100A8 and S100A9 in livers treated with Panc02-H7-derived exosomes. Histogram shows expression of the three proteins in three groupsas determined by densitometric analysis (n=3/group). (D) Pancreatic cancer-derived exosomes induce MDSC accumulation in peripheral blood. (E) Representative flow cytometric plots (left) and quantification (right) of CD11b + GR1 + MDSCs (n=5/group). *P<0.05, **P<0.01,***P<0.001.

    Article Snippet: Primary antibodies against fibronectin (1:100),α-SMA (1:50), S100A8 (1:50), S100A9 (1:50), and F4/80 (1:50) were purchased from Proteintech (Wuhan, China).

    Techniques: Confocal Microscopy, Labeling, Staining, Expressing, Western Blot, Derivative Assay

    IHC analysis and histopathological examination of macrophages (F4/80), hStCs (α-SMA), and neutrophils in liver metastatic niches of naïve mice and mice treated with PBS, Panc02 EXOs, or Panc02-H7 EXOs at 30d post-SOI (arrow shows neutrophils in liver) (A) . Representative histogram shows quantification of F4/80 + macrophages, α-SMA + hStCs, and neutrophils (B) . Identification of FN, S100A8, and S100A9 as inflammatory mediators, and collagen deposition in the liver metastatic niche (C) . Representative histogram shows FN and MTS quantification (D) . Representative histogram shows S100A8 and S100A9 quantification (E) . n=6/group.**P<0.01,***P<0.001.10 fields assessed per sample. FOV, field of view.

    Journal: Oncotarget

    Article Title: Pancreatic cancer-derived exosomes promote tumor metastasis and liver pre-metastatic niche formation

    doi: 10.18632/oncotarget.18831

    Figure Lengend Snippet: IHC analysis and histopathological examination of macrophages (F4/80), hStCs (α-SMA), and neutrophils in liver metastatic niches of naïve mice and mice treated with PBS, Panc02 EXOs, or Panc02-H7 EXOs at 30d post-SOI (arrow shows neutrophils in liver) (A) . Representative histogram shows quantification of F4/80 + macrophages, α-SMA + hStCs, and neutrophils (B) . Identification of FN, S100A8, and S100A9 as inflammatory mediators, and collagen deposition in the liver metastatic niche (C) . Representative histogram shows FN and MTS quantification (D) . Representative histogram shows S100A8 and S100A9 quantification (E) . n=6/group.**P<0.01,***P<0.001.10 fields assessed per sample. FOV, field of view.

    Article Snippet: Primary antibodies against fibronectin (1:100),α-SMA (1:50), S100A8 (1:50), S100A9 (1:50), and F4/80 (1:50) were purchased from Proteintech (Wuhan, China).

    Techniques:

    PPI network and the significant module of DEGs. (A) The PPI network of DEGs. (B) The significant module was obtained from PPI network constructed using Cytoscape with 13 nodes and 57 edges. S100A8 is marked in yellow, and downregulated genes are marked in green.

    Journal: Frontiers in Immunology

    Article Title: Glomerular Expression of S100A8 in Lupus Nephritis: An Integrated Bioinformatics Analysis

    doi: 10.3389/fimmu.2022.843576

    Figure Lengend Snippet: PPI network and the significant module of DEGs. (A) The PPI network of DEGs. (B) The significant module was obtained from PPI network constructed using Cytoscape with 13 nodes and 57 edges. S100A8 is marked in yellow, and downregulated genes are marked in green.

    Article Snippet: The mouse anti-S100A8 antibody (Proteintech Group, Inc., Chicago, IL, USA) was used.

    Techniques: Construct

    Clinical and laboratory information of the LN patients.

    Journal: Frontiers in Immunology

    Article Title: Glomerular Expression of S100A8 in Lupus Nephritis: An Integrated Bioinformatics Analysis

    doi: 10.3389/fimmu.2022.843576

    Figure Lengend Snippet: Clinical and laboratory information of the LN patients.

    Article Snippet: The mouse anti-S100A8 antibody (Proteintech Group, Inc., Chicago, IL, USA) was used.

    Techniques:

    Glomerular expression of S100A8 in various ISN/RPS class LN patients.

    Journal: Frontiers in Immunology

    Article Title: Glomerular Expression of S100A8 in Lupus Nephritis: An Integrated Bioinformatics Analysis

    doi: 10.3389/fimmu.2022.843576

    Figure Lengend Snippet: Glomerular expression of S100A8 in various ISN/RPS class LN patients.

    Article Snippet: The mouse anti-S100A8 antibody (Proteintech Group, Inc., Chicago, IL, USA) was used.

    Techniques: Expressing

    Glomerular expression of  S100A8  in various ISN/RPS class LN patients.

    Journal: Frontiers in Immunology

    Article Title: Glomerular Expression of S100A8 in Lupus Nephritis: An Integrated Bioinformatics Analysis

    doi: 10.3389/fimmu.2022.843576

    Figure Lengend Snippet: Glomerular expression of S100A8 in various ISN/RPS class LN patients.

    Article Snippet: The mouse anti-S100A8 antibody (Proteintech Group, Inc., Chicago, IL, USA) was used.

    Techniques: Expressing

    The correlation of glomerular expression of S100A8 with clinical and laboratory data. *P < 0.05; **P < 0.01;***P < 0.001.

    Journal: Frontiers in Immunology

    Article Title: Glomerular Expression of S100A8 in Lupus Nephritis: An Integrated Bioinformatics Analysis

    doi: 10.3389/fimmu.2022.843576

    Figure Lengend Snippet: The correlation of glomerular expression of S100A8 with clinical and laboratory data. *P < 0.05; **P < 0.01;***P < 0.001.

    Article Snippet: The mouse anti-S100A8 antibody (Proteintech Group, Inc., Chicago, IL, USA) was used.

    Techniques: Expressing

    Sequential recruitment of histone modifying enzymes by BRG1. (A–D) EAhy926 cells were transfected with siRNA targeting BRG1 or scrambled siRNA (SCR) followed by treatment with Ang II (1 μM). Cells were harvested at indicated time points and ChIP assays were performed with anti-acetyl H3 (A) , anti-dimethyl H3K9 (B) , anti-p300 (C) , or anti-KDM3A (D) . All experiments were repeated three times and one representative experiment is shown. Error bars represent SD (* p < 0.05, one-way ANOVA with post hoc Scheffe test).

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: BRG1 Stimulates Endothelial Derived Alarmin MRP8 to Promote Macrophage Infiltration in an Animal Model of Cardiac Hypertrophy

    doi: 10.3389/fcell.2020.00569

    Figure Lengend Snippet: Sequential recruitment of histone modifying enzymes by BRG1. (A–D) EAhy926 cells were transfected with siRNA targeting BRG1 or scrambled siRNA (SCR) followed by treatment with Ang II (1 μM). Cells were harvested at indicated time points and ChIP assays were performed with anti-acetyl H3 (A) , anti-dimethyl H3K9 (B) , anti-p300 (C) , or anti-KDM3A (D) . All experiments were repeated three times and one representative experiment is shown. Error bars represent SD (* p < 0.05, one-way ANOVA with post hoc Scheffe test).

    Article Snippet: Western blot analyses were performed with anti-BRG1 (Santa Cruz, sc-10768), anti-MRP8 (Proteintech, 15792-1-AP), anti-HIF-1α (Santa Cruz, sc-10790), anti-p300 (Santa Cruz, sc-585), anti-KDM3A (Proteintech, 15792-1-AP), and anti-β-actin (Sigma, A2228) antibodies.

    Techniques: Transfection

    p300 and KDM3A contributes to MRP8 trans- activation. (A–C) EAhy926 cells were transfected with indicated siRNAs or scrambled siRNA (SCR) followed by treatment with Ang II (1 μM). MRP8 expression was examined by qPCR and Western. Macrophage migration was examined by transwell assay. (D) A schematic model.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: BRG1 Stimulates Endothelial Derived Alarmin MRP8 to Promote Macrophage Infiltration in an Animal Model of Cardiac Hypertrophy

    doi: 10.3389/fcell.2020.00569

    Figure Lengend Snippet: p300 and KDM3A contributes to MRP8 trans- activation. (A–C) EAhy926 cells were transfected with indicated siRNAs or scrambled siRNA (SCR) followed by treatment with Ang II (1 μM). MRP8 expression was examined by qPCR and Western. Macrophage migration was examined by transwell assay. (D) A schematic model.

    Article Snippet: Western blot analyses were performed with anti-BRG1 (Santa Cruz, sc-10768), anti-MRP8 (Proteintech, 15792-1-AP), anti-HIF-1α (Santa Cruz, sc-10790), anti-p300 (Santa Cruz, sc-585), anti-KDM3A (Proteintech, 15792-1-AP), and anti-β-actin (Sigma, A2228) antibodies.

    Techniques: Activation Assay, Transfection, Expressing, Western Blot, Migration, Transwell Assay