rabbit anti-nox2 Search Results


90
Epitomics corp prohibitin antibody
Prohibitin Antibody, supplied by Epitomics corp, 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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Abnova rabbit anti-nox2
Rabbit Anti Nox2, supplied by Abnova, 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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Average 90 stars, based on 1 article reviews
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Bioworld Antibodies rabbit polyclonal anti-nox4
Rabbit Polyclonal Anti Nox4, supplied by Bioworld Antibodies, 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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86
Huabio Inc anti nox2 gp91phox recombinant rabbit monoclonal antibody
Bayesian networks and KEGG suggest a CCF-biased reorganization toward CR3-SYK-NOX/NET pathways relative to IPA/AmB. The network analysis highlights recurrent CCF-associated hub genes, including Itgam, Syk, Rac2, and <t>Cybb,</t> together with pathway enrichment linked to oxidative and NET-related responses. ( A ) Hub gene networks identified in the IPA, CCF, and AmB groups by Bayesian network analysis. Genes were ranked by DEGREE value, with the top 10% defined as hub genes and marked in color; nodes with DEGREE >6 were placed at the core of the network. ( B ) KEGG pathway enrichment of hub genes in each group. Pathways were ranked by −log 10 ( p value). Bar colors represent different groups: IPA (dark blue), CCF (dark red), and AmB (light blue). The red box denotes the most significantly enriched KEGG pathway in the CCF group. ( C ) FPKM values of key CCF-regulated genes at +2, +4, and +6 dpi. Statistical analysis was conducted comparing all groups to the CCF group. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 indicate levels of statistical significance. ( D ) qPCR validation of key CCF-regulated genes in each group. Statistical analysis was conducted using one-way ANOVA, comparing all groups to the CCF group. * p < 0.05, ** p < 0.01, **** p < 0.0001 indicate levels of statistical significance. Data are presented as mean ± SD from n = 3 mice per group.
Anti Nox2 Gp91phox Recombinant Rabbit Monoclonal Antibody, supplied by Huabio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Bayesian networks and KEGG suggest a CCF-biased reorganization toward CR3-SYK-NOX/NET pathways relative to IPA/AmB. The network analysis highlights recurrent CCF-associated hub genes, including Itgam, Syk, Rac2, and Cybb, together with pathway enrichment linked to oxidative and NET-related responses. ( A ) Hub gene networks identified in the IPA, CCF, and AmB groups by Bayesian network analysis. Genes were ranked by DEGREE value, with the top 10% defined as hub genes and marked in color; nodes with DEGREE >6 were placed at the core of the network. ( B ) KEGG pathway enrichment of hub genes in each group. Pathways were ranked by −log 10 ( p value). Bar colors represent different groups: IPA (dark blue), CCF (dark red), and AmB (light blue). The red box denotes the most significantly enriched KEGG pathway in the CCF group. ( C ) FPKM values of key CCF-regulated genes at +2, +4, and +6 dpi. Statistical analysis was conducted comparing all groups to the CCF group. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 indicate levels of statistical significance. ( D ) qPCR validation of key CCF-regulated genes in each group. Statistical analysis was conducted using one-way ANOVA, comparing all groups to the CCF group. * p < 0.05, ** p < 0.01, **** p < 0.0001 indicate levels of statistical significance. Data are presented as mean ± SD from n = 3 mice per group.

Journal: Current Issues in Molecular Biology

Article Title: Coptis chinensis Franch. Suppresses Invasive Pulmonary Aspergillosis by Augmenting NADPH-Dependent Neutrophil Extracellular Traps via Dual Modulation of Complement Activation and Gut Microbiota

doi: 10.3390/cimb48040424

Figure Lengend Snippet: Bayesian networks and KEGG suggest a CCF-biased reorganization toward CR3-SYK-NOX/NET pathways relative to IPA/AmB. The network analysis highlights recurrent CCF-associated hub genes, including Itgam, Syk, Rac2, and Cybb, together with pathway enrichment linked to oxidative and NET-related responses. ( A ) Hub gene networks identified in the IPA, CCF, and AmB groups by Bayesian network analysis. Genes were ranked by DEGREE value, with the top 10% defined as hub genes and marked in color; nodes with DEGREE >6 were placed at the core of the network. ( B ) KEGG pathway enrichment of hub genes in each group. Pathways were ranked by −log 10 ( p value). Bar colors represent different groups: IPA (dark blue), CCF (dark red), and AmB (light blue). The red box denotes the most significantly enriched KEGG pathway in the CCF group. ( C ) FPKM values of key CCF-regulated genes at +2, +4, and +6 dpi. Statistical analysis was conducted comparing all groups to the CCF group. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 indicate levels of statistical significance. ( D ) qPCR validation of key CCF-regulated genes in each group. Statistical analysis was conducted using one-way ANOVA, comparing all groups to the CCF group. * p < 0.05, ** p < 0.01, **** p < 0.0001 indicate levels of statistical significance. Data are presented as mean ± SD from n = 3 mice per group.

Article Snippet: Primary antibodies used in Western Blot included Beta Actin Monoclonal antibody (66009-1-Ig, Proteintech, Wuhan, China), NCF4/p40phox Rabbit pAb (A2096, Abclonal, Wuhan, China), Anti-NOX2/gp91phox Recombinant Rabbit Monoclonal Antibody (ET1611-44, Huabio, Hangzhou, China), RAC2 Rabbit pAb (A1139, Abclonal, China) and Anti-NCF1/p47phox Rabbit pAb (GB11724, Servicebio, Wuhan, China).

Techniques: Biomarker Discovery

CCF enhances NOX2 components and its benefit is partially attenuated by apocynin, consistent with oxidative pathway involvement. This figure combines protein, survival, and fungal-burden data to show partial pharmacological support for the role of oxidative responses in CCF-mediated protection. ( A ) Protein expression of NADPH oxidase subunits in lung tissue at +4 dpi as detected by Western blot. I, IPA group; C, CCF group; A, AmB group; M, Marker. Data are presented as mean ± SD from n = 5 mice per group. ( B ) Densitometric quantification of protein levels normalized to β-ACTIN. Statistical analysis was performed using one-way ANOVA with multiple comparisons. * p < 0.05. Data are presented as mean ± SD from n = 5 mice per group. ( C ) Survival curves of mice up to +8 dpi. CCF significantly improved survival compared to the IPA group. Co-treatment with the NADPH oxidase inhibitor apocynin partially reversed this effect. * p < 0.05, ** p < 0.01. Survival data were analyzed using the Kaplan–Meier method with n = 10 mice per group. ( D ) Fungal burden in lung tissues at +4 dpi measured by colony-forming unit counts. Statistical analysis was performed using one-way ANOVA with multiple comparisons. * p < 0.05. Data are presented as mean ± SD from n = 5 mice per group.

Journal: Current Issues in Molecular Biology

Article Title: Coptis chinensis Franch. Suppresses Invasive Pulmonary Aspergillosis by Augmenting NADPH-Dependent Neutrophil Extracellular Traps via Dual Modulation of Complement Activation and Gut Microbiota

doi: 10.3390/cimb48040424

Figure Lengend Snippet: CCF enhances NOX2 components and its benefit is partially attenuated by apocynin, consistent with oxidative pathway involvement. This figure combines protein, survival, and fungal-burden data to show partial pharmacological support for the role of oxidative responses in CCF-mediated protection. ( A ) Protein expression of NADPH oxidase subunits in lung tissue at +4 dpi as detected by Western blot. I, IPA group; C, CCF group; A, AmB group; M, Marker. Data are presented as mean ± SD from n = 5 mice per group. ( B ) Densitometric quantification of protein levels normalized to β-ACTIN. Statistical analysis was performed using one-way ANOVA with multiple comparisons. * p < 0.05. Data are presented as mean ± SD from n = 5 mice per group. ( C ) Survival curves of mice up to +8 dpi. CCF significantly improved survival compared to the IPA group. Co-treatment with the NADPH oxidase inhibitor apocynin partially reversed this effect. * p < 0.05, ** p < 0.01. Survival data were analyzed using the Kaplan–Meier method with n = 10 mice per group. ( D ) Fungal burden in lung tissues at +4 dpi measured by colony-forming unit counts. Statistical analysis was performed using one-way ANOVA with multiple comparisons. * p < 0.05. Data are presented as mean ± SD from n = 5 mice per group.

Article Snippet: Primary antibodies used in Western Blot included Beta Actin Monoclonal antibody (66009-1-Ig, Proteintech, Wuhan, China), NCF4/p40phox Rabbit pAb (A2096, Abclonal, Wuhan, China), Anti-NOX2/gp91phox Recombinant Rabbit Monoclonal Antibody (ET1611-44, Huabio, Hangzhou, China), RAC2 Rabbit pAb (A1139, Abclonal, China) and Anti-NCF1/p47phox Rabbit pAb (GB11724, Servicebio, Wuhan, China).

Techniques: Expressing, Western Blot, Marker

CCF-treated mice show microbiota remodeling with enrichment of Clostridium sp., and observed Cybb/Syk associations are non-causal. The main features of this figure are the distinct clustering of gut microbial communities across groups, the selective enrichment of Clostridium sp. in the CCF group, and its positive correlation with the redox-related host genes Cybb and Syk . ( A ) Alpha diversity analysis using the Chao1 index and Shannon index reveals significant differences among CN, IPA, CCF, and AmB groups. ( B ) Principal coordinates analysis (PCoA) based on weighted UniFrac distances demonstrates distinct clustering of gut microbial communities across groups. ( C ) Taxonomic composition profiles at the family genus, and species levels. Bar plots display the relative abundance of dominant taxa within each group. ( D ) Histogram of LDA scores (log 10 ) for discriminative features, indicating significantly enriched taxa in each group. The colors represent different groups: CN (blue), IPA (red), CCF (green), and AmB (purple). ( E ) Cladogram representing the phylogenetic distribution of differentially abundant taxa among the groups. Colored nodes represent taxa significantly enriched in the corresponding groups: CN (blue), IPA (red), CCF (green), and AmB (purple). From inner to outer circles represent phylum, class, order, family, genus, and species levels. Taxa connected by the same color belong to the same species. ( F ) Comparison of the abundances of significantly different biomarkers: g__ Parasutterella and s__ Lactobacillus in the CN group, s__ Clostridium_sp in the CCF group, g__ Clostridia in the AmB group, and significantly deleted biomarkers g__ Muribaculaceae and g__ Lachnospiraceae in the CCF group. ( G ) Spearman correlation analysis between Clostridium sp. abundance and the expression levels of NADPH oxidase-related genes. Scatter plots show strong positive correlations with Cybb (R = 0.81, p = 0.0076) and Syk (R = 0.75, p = 0.021).

Journal: Current Issues in Molecular Biology

Article Title: Coptis chinensis Franch. Suppresses Invasive Pulmonary Aspergillosis by Augmenting NADPH-Dependent Neutrophil Extracellular Traps via Dual Modulation of Complement Activation and Gut Microbiota

doi: 10.3390/cimb48040424

Figure Lengend Snippet: CCF-treated mice show microbiota remodeling with enrichment of Clostridium sp., and observed Cybb/Syk associations are non-causal. The main features of this figure are the distinct clustering of gut microbial communities across groups, the selective enrichment of Clostridium sp. in the CCF group, and its positive correlation with the redox-related host genes Cybb and Syk . ( A ) Alpha diversity analysis using the Chao1 index and Shannon index reveals significant differences among CN, IPA, CCF, and AmB groups. ( B ) Principal coordinates analysis (PCoA) based on weighted UniFrac distances demonstrates distinct clustering of gut microbial communities across groups. ( C ) Taxonomic composition profiles at the family genus, and species levels. Bar plots display the relative abundance of dominant taxa within each group. ( D ) Histogram of LDA scores (log 10 ) for discriminative features, indicating significantly enriched taxa in each group. The colors represent different groups: CN (blue), IPA (red), CCF (green), and AmB (purple). ( E ) Cladogram representing the phylogenetic distribution of differentially abundant taxa among the groups. Colored nodes represent taxa significantly enriched in the corresponding groups: CN (blue), IPA (red), CCF (green), and AmB (purple). From inner to outer circles represent phylum, class, order, family, genus, and species levels. Taxa connected by the same color belong to the same species. ( F ) Comparison of the abundances of significantly different biomarkers: g__ Parasutterella and s__ Lactobacillus in the CN group, s__ Clostridium_sp in the CCF group, g__ Clostridia in the AmB group, and significantly deleted biomarkers g__ Muribaculaceae and g__ Lachnospiraceae in the CCF group. ( G ) Spearman correlation analysis between Clostridium sp. abundance and the expression levels of NADPH oxidase-related genes. Scatter plots show strong positive correlations with Cybb (R = 0.81, p = 0.0076) and Syk (R = 0.75, p = 0.021).

Article Snippet: Primary antibodies used in Western Blot included Beta Actin Monoclonal antibody (66009-1-Ig, Proteintech, Wuhan, China), NCF4/p40phox Rabbit pAb (A2096, Abclonal, Wuhan, China), Anti-NOX2/gp91phox Recombinant Rabbit Monoclonal Antibody (ET1611-44, Huabio, Hangzhou, China), RAC2 Rabbit pAb (A1139, Abclonal, China) and Anti-NCF1/p47phox Rabbit pAb (GB11724, Servicebio, Wuhan, China).

Techniques: Comparison, Expressing