15-792 Search Results


90
ATCC s heerlen atcc 15792
S Heerlen Atcc 15792, supplied by ATCC, 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/result/s heerlen atcc 15792/product/ATCC
Average 90 stars, based on 1 article reviews
s heerlen atcc 15792 - by Bioz Stars, 2025-02
90/100 stars
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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
s100a8 - by Bioz Stars, 2025-02
93/100 stars
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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
mouse anti s100a8 antibody - by Bioz Stars, 2025-02
93/100 stars
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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
anti kdm3a - by Bioz Stars, 2025-02
93/100 stars
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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