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Diagnostic BioSystems polyvuetm plus kit
Polyvuetm Plus Kit, supplied by Diagnostic BioSystems, 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/codex+staining+kit/polyvuetm+plus+kit/pm38667457-67-10-16
Average 90 stars, based on 1 article reviews
polyvuetm plus kit - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Immunohistochemical staining:

Article Title: Overexpression of Connexin 40 in the Vascular Endothelial Cells of Placenta with Acute Chorioamnionitis.
Article Snippet: .. Immunohistochemical staining was performed following the protocol from Diagnostic BioSystems PolyVueTM Plus Kit (Code No. PVP250D, Diagnostic BioSystems, Pleasanton, CA, USA). .. Primary antibodies were diluted to optimal concentration using the antibody diluent, Dako REALTM (Code No. S2022, Dako, Groschup, Denmark).

Staining:

Article Title: Overexpression of Connexin 40 in the Vascular Endothelial Cells of Placenta with Acute Chorioamnionitis.
Article Snippet: .. Immunohistochemical staining was performed following the protocol from Diagnostic BioSystems PolyVueTM Plus Kit (Code No. PVP250D, Diagnostic BioSystems, Pleasanton, CA, USA). .. Primary antibodies were diluted to optimal concentration using the antibody diluent, Dako REALTM (Code No. S2022, Dako, Groschup, Denmark).

other:

Article Title: Overexpression of Connexin 40 in the Vascular Endothelial Cells of Placenta with Acute Chorioamnionitis.
Article Snippet: Sections were then incubated with PolyVueTM (Enhancer) (Code No. PVP250D, Diagnostic BioSystems, Pleasanton, CA 94588, USA) for 30 min followed by washing.



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KITL regulates PSC state and pancreas tissue homeostasis. A, Volcano plot of all upregulated, nonsignificant, and downregulated differentially expressed genes (DEG) as defined by the Wald test ( P .adj < 0.05 and log 2 FC > 1) from Kitl overexpression ( Kitl OE) ImPSC-1 bulk RNA-seq dataset with representative gene labels included. Data represent three biological repeats. B, Gene ontology (GO) analysis of upregulated and downregulated genes in immortalized PSCs (ImPSC-1) overexpressing Kitl . Top 10 enrichment categories ranked by adjusted P values plotted in each direction. C, qRT-PCR analysis of indicated DEGs in ImPSC-1 expressing stable Kitl knockdown (sh Kitl ) or overexpression ( Kitl OE). PLKO vector (shCtrl) and fluorescence overexpression ( Egfp OE) serves as the respective control. D, Representative images of <t>CODEX</t> <t>staining</t> (left) and quantification (right) for GFP (green) and CD31 (red) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 3–4 mice per arm). Scale bar, 100 μm. E, Representative images of CODEX composite staining (left) and quantification (right) for CD45 (white) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 4 mice per arm). Scale bar, 50 μm. F, Representative images of IHC staining for GFP (green), c-KIT receptor (KIT, red), and VIM (magenta) in healthy murine pancreas from Rosa26 mTmG/+ ;Fabp4-Cre mice. Scale bar, 10 μm. G, Representative images of IHC staining for CD31 (green) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. H, Representative images of IHC staining for panCK (white) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. I, Representative hematoxylin and eosin images between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. J, Representative images of IHC staining (left) for panCK (green) and amylase (red) between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 10 μm. PanCK quantification on right ( n = 3 mice per arm). K, Representative IHC images (left) and quantification (right) for CD45 staining between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. L, Representative images (left) and quantification (right) for CD68 staining in caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mouse pancreas. The same co-stained tissue section is shown in K and L . Scale bar, 100 μm. For comparisons of two groups, an unpaired t test was used. For comparisons of more than two groups with one independent variable, the one-way ANOVA test was used. Data are represented as mean ± SEM; *, P ≤ 0.05; **, P ≤ 0.01; ***, P ≤ 0.001; ****, P ≤ 0.0001; FC, fold changes; ns, not significant; panc area, pancreas.
Codex Staining Kit, supplied by Akoya Biosciences, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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KITL regulates PSC state and pancreas tissue homeostasis. A, Volcano plot of all upregulated, nonsignificant, and downregulated differentially expressed genes (DEG) as defined by the Wald test ( P .adj < 0.05 and log 2 FC > 1) from Kitl overexpression ( Kitl OE) ImPSC-1 bulk RNA-seq dataset with representative gene labels included. Data represent three biological repeats. B, Gene ontology (GO) analysis of upregulated and downregulated genes in immortalized PSCs (ImPSC-1) overexpressing Kitl . Top 10 enrichment categories ranked by adjusted P values plotted in each direction. C, qRT-PCR analysis of indicated DEGs in ImPSC-1 expressing stable Kitl knockdown (sh Kitl ) or overexpression ( Kitl OE). PLKO vector (shCtrl) and fluorescence overexpression ( Egfp OE) serves as the respective control. D, Representative images of <t>CODEX</t> <t>staining</t> (left) and quantification (right) for GFP (green) and CD31 (red) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 3–4 mice per arm). Scale bar, 100 μm. E, Representative images of CODEX composite staining (left) and quantification (right) for CD45 (white) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 4 mice per arm). Scale bar, 50 μm. F, Representative images of IHC staining for GFP (green), c-KIT receptor (KIT, red), and VIM (magenta) in healthy murine pancreas from Rosa26 mTmG/+ ;Fabp4-Cre mice. Scale bar, 10 μm. G, Representative images of IHC staining for CD31 (green) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. H, Representative images of IHC staining for panCK (white) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. I, Representative hematoxylin and eosin images between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. J, Representative images of IHC staining (left) for panCK (green) and amylase (red) between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 10 μm. PanCK quantification on right ( n = 3 mice per arm). K, Representative IHC images (left) and quantification (right) for CD45 staining between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. L, Representative images (left) and quantification (right) for CD68 staining in caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mouse pancreas. The same co-stained tissue section is shown in K and L . Scale bar, 100 μm. For comparisons of two groups, an unpaired t test was used. For comparisons of more than two groups with one independent variable, the one-way ANOVA test was used. Data are represented as mean ± SEM; *, P ≤ 0.05; **, P ≤ 0.01; ***, P ≤ 0.001; ****, P ≤ 0.0001; FC, fold changes; ns, not significant; panc area, pancreas.
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KITL regulates PSC state and pancreas tissue homeostasis. A, Volcano plot of all upregulated, nonsignificant, and downregulated differentially expressed genes (DEG) as defined by the Wald test ( P .adj < 0.05 and log 2 FC > 1) from Kitl overexpression ( Kitl OE) ImPSC-1 bulk RNA-seq dataset with representative gene labels included. Data represent three biological repeats. B, Gene ontology (GO) analysis of upregulated and downregulated genes in immortalized PSCs (ImPSC-1) overexpressing Kitl . Top 10 enrichment categories ranked by adjusted P values plotted in each direction. C, qRT-PCR analysis of indicated DEGs in ImPSC-1 expressing stable Kitl knockdown (sh Kitl ) or overexpression ( Kitl OE). PLKO vector (shCtrl) and fluorescence overexpression ( Egfp OE) serves as the respective control. D, Representative images of <t>CODEX</t> <t>staining</t> (left) and quantification (right) for GFP (green) and CD31 (red) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 3–4 mice per arm). Scale bar, 100 μm. E, Representative images of CODEX composite staining (left) and quantification (right) for CD45 (white) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 4 mice per arm). Scale bar, 50 μm. F, Representative images of IHC staining for GFP (green), c-KIT receptor (KIT, red), and VIM (magenta) in healthy murine pancreas from Rosa26 mTmG/+ ;Fabp4-Cre mice. Scale bar, 10 μm. G, Representative images of IHC staining for CD31 (green) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. H, Representative images of IHC staining for panCK (white) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. I, Representative hematoxylin and eosin images between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. J, Representative images of IHC staining (left) for panCK (green) and amylase (red) between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 10 μm. PanCK quantification on right ( n = 3 mice per arm). K, Representative IHC images (left) and quantification (right) for CD45 staining between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. L, Representative images (left) and quantification (right) for CD68 staining in caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mouse pancreas. The same co-stained tissue section is shown in K and L . Scale bar, 100 μm. For comparisons of two groups, an unpaired t test was used. For comparisons of more than two groups with one independent variable, the one-way ANOVA test was used. Data are represented as mean ± SEM; *, P ≤ 0.05; **, P ≤ 0.01; ***, P ≤ 0.001; ****, P ≤ 0.0001; FC, fold changes; ns, not significant; panc area, pancreas.
Codex Staining Kit, supplied by Technical Manufacturing Company, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


KITL regulates PSC state and pancreas tissue homeostasis. A, Volcano plot of all upregulated, nonsignificant, and downregulated differentially expressed genes (DEG) as defined by the Wald test ( P .adj < 0.05 and log 2 FC > 1) from Kitl overexpression ( Kitl OE) ImPSC-1 bulk RNA-seq dataset with representative gene labels included. Data represent three biological repeats. B, Gene ontology (GO) analysis of upregulated and downregulated genes in immortalized PSCs (ImPSC-1) overexpressing Kitl . Top 10 enrichment categories ranked by adjusted P values plotted in each direction. C, qRT-PCR analysis of indicated DEGs in ImPSC-1 expressing stable Kitl knockdown (sh Kitl ) or overexpression ( Kitl OE). PLKO vector (shCtrl) and fluorescence overexpression ( Egfp OE) serves as the respective control. D, Representative images of CODEX staining (left) and quantification (right) for GFP (green) and CD31 (red) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 3–4 mice per arm). Scale bar, 100 μm. E, Representative images of CODEX composite staining (left) and quantification (right) for CD45 (white) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 4 mice per arm). Scale bar, 50 μm. F, Representative images of IHC staining for GFP (green), c-KIT receptor (KIT, red), and VIM (magenta) in healthy murine pancreas from Rosa26 mTmG/+ ;Fabp4-Cre mice. Scale bar, 10 μm. G, Representative images of IHC staining for CD31 (green) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. H, Representative images of IHC staining for panCK (white) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. I, Representative hematoxylin and eosin images between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. J, Representative images of IHC staining (left) for panCK (green) and amylase (red) between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 10 μm. PanCK quantification on right ( n = 3 mice per arm). K, Representative IHC images (left) and quantification (right) for CD45 staining between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. L, Representative images (left) and quantification (right) for CD68 staining in caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mouse pancreas. The same co-stained tissue section is shown in K and L . Scale bar, 100 μm. For comparisons of two groups, an unpaired t test was used. For comparisons of more than two groups with one independent variable, the one-way ANOVA test was used. Data are represented as mean ± SEM; *, P ≤ 0.05; **, P ≤ 0.01; ***, P ≤ 0.001; ****, P ≤ 0.0001; FC, fold changes; ns, not significant; panc area, pancreas.

Journal: Cancer Discovery

Article Title: Stromal KITL/SCF Maintains Pancreas Tissue Homeostasis and Restrains Tumor Progression

doi: 10.1158/2159-8290.CD-24-1079

Figure Lengend Snippet: KITL regulates PSC state and pancreas tissue homeostasis. A, Volcano plot of all upregulated, nonsignificant, and downregulated differentially expressed genes (DEG) as defined by the Wald test ( P .adj < 0.05 and log 2 FC > 1) from Kitl overexpression ( Kitl OE) ImPSC-1 bulk RNA-seq dataset with representative gene labels included. Data represent three biological repeats. B, Gene ontology (GO) analysis of upregulated and downregulated genes in immortalized PSCs (ImPSC-1) overexpressing Kitl . Top 10 enrichment categories ranked by adjusted P values plotted in each direction. C, qRT-PCR analysis of indicated DEGs in ImPSC-1 expressing stable Kitl knockdown (sh Kitl ) or overexpression ( Kitl OE). PLKO vector (shCtrl) and fluorescence overexpression ( Egfp OE) serves as the respective control. D, Representative images of CODEX staining (left) and quantification (right) for GFP (green) and CD31 (red) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 3–4 mice per arm). Scale bar, 100 μm. E, Representative images of CODEX composite staining (left) and quantification (right) for CD45 (white) in normal pancreas from Fabp4-Cre or Kitl fl/fl ;Fabp4-Cre mouse model ( n = 4 mice per arm). Scale bar, 50 μm. F, Representative images of IHC staining for GFP (green), c-KIT receptor (KIT, red), and VIM (magenta) in healthy murine pancreas from Rosa26 mTmG/+ ;Fabp4-Cre mice. Scale bar, 10 μm. G, Representative images of IHC staining for CD31 (green) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. H, Representative images of IHC staining for panCK (white) and c-KIT receptor (KIT, red) in healthy murine pancreas. Scale bar, 10 μm. I, Representative hematoxylin and eosin images between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. J, Representative images of IHC staining (left) for panCK (green) and amylase (red) between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 10 μm. PanCK quantification on right ( n = 3 mice per arm). K, Representative IHC images (left) and quantification (right) for CD45 staining between caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mice. Scale bar, 100 μm. L, Representative images (left) and quantification (right) for CD68 staining in caerulein-treated Fabp4-Cre and Kitl fl/fl ;Fabp4-Cre mouse pancreas. The same co-stained tissue section is shown in K and L . Scale bar, 100 μm. For comparisons of two groups, an unpaired t test was used. For comparisons of more than two groups with one independent variable, the one-way ANOVA test was used. Data are represented as mean ± SEM; *, P ≤ 0.05; **, P ≤ 0.01; ***, P ≤ 0.001; ****, P ≤ 0.0001; FC, fold changes; ns, not significant; panc area, pancreas.

Article Snippet: In brief, 5-μm FFPE pancreas sections were mounted onto 22 × 22 mm glass coverslips (Electron Microscopy Sciences) coated in 0.1% poly-L-lysine (Sigma-Aldrich) and stained with using CODEX Staining Kit (Akoya Biosciences).

Techniques: Over Expression, RNA Sequencing, Quantitative RT-PCR, Expressing, Knockdown, Plasmid Preparation, Fluorescence, Control, Staining, Immunohistochemistry