originpro 8® software version 9.75 Search Results


94
Miltenyi Biotec eosinophil isolation buffer
Healthy human eosinophils have a gene expression profile distinct from other MNCs and granulocytes (A) Experimental schema to obtain scRNA-seq of asthmatic and healthy <t>eosinophil</t> and mononuclear cells. (B) UMAP plot of healthy eosinophils, neutrophils, and mononuclear cells ( n = 51,400). (C) Heatmap of averaged expression of top 500 most significant healthy eosinophil marker genes (Padj <0.05, log2FC > 0.25). Scale represents gene expression Z score. (D) Violin plots of gene expression for canonical eosinophil markers. Adjusted p -values from differential expression testing (Wilcoxon rank-sum test). (E) Heatmap of averaged expression of 154 degranulation pathway genes. Scale represents gene expression Z score.
Eosinophil Isolation Buffer, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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JASCO Inc high performance liquid chromatography hplc system
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
High Performance Liquid Chromatography Hplc System, supplied by JASCO Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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OriginLab corp originpro 8® software version 9.75
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Originpro 8® Software Version 9.75, supplied by OriginLab 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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Eppendorf AG thermomixer
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Thermomixer, supplied by Eppendorf AG, 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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gel  (Bio-Rad)
98
Bio-Rad gel
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Gel, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher co2 gas bottle n4.5
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Co2 Gas Bottle N4.5, supplied by Thermo Fisher, 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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CH Instruments likelihood ratio chi-sq
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Likelihood Ratio Chi Sq, supplied by CH Instruments, 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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Bruker Corporation spinworks 2.5
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Spinworks 2.5, supplied by Bruker Corporation, 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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Illumina Inc sentrix humanref-8 expression beadchips
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Sentrix Humanref 8 Expression Beadchips, supplied by Illumina Inc, 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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Alphamed INC theoncologist
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Theoncologist, supplied by Alphamed INC, 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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Millipore borane-pyridine
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
Borane Pyridine, supplied by Millipore, 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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Ubichem Inc 8-bromo-4-chloroquinoline
Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by <t>HPLC.</t> Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.
8 Bromo 4 Chloroquinoline, supplied by Ubichem Inc, 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


Healthy human eosinophils have a gene expression profile distinct from other MNCs and granulocytes (A) Experimental schema to obtain scRNA-seq of asthmatic and healthy eosinophil and mononuclear cells. (B) UMAP plot of healthy eosinophils, neutrophils, and mononuclear cells ( n = 51,400). (C) Heatmap of averaged expression of top 500 most significant healthy eosinophil marker genes (Padj <0.05, log2FC > 0.25). Scale represents gene expression Z score. (D) Violin plots of gene expression for canonical eosinophil markers. Adjusted p -values from differential expression testing (Wilcoxon rank-sum test). (E) Heatmap of averaged expression of 154 degranulation pathway genes. Scale represents gene expression Z score.

Journal: iScience

Article Title: Single-cell RNA-sequencing of circulating eosinophils from asthma patients reveals an inflammatory signature

doi: 10.1016/j.isci.2025.112609

Figure Lengend Snippet: Healthy human eosinophils have a gene expression profile distinct from other MNCs and granulocytes (A) Experimental schema to obtain scRNA-seq of asthmatic and healthy eosinophil and mononuclear cells. (B) UMAP plot of healthy eosinophils, neutrophils, and mononuclear cells ( n = 51,400). (C) Heatmap of averaged expression of top 500 most significant healthy eosinophil marker genes (Padj <0.05, log2FC > 0.25). Scale represents gene expression Z score. (D) Violin plots of gene expression for canonical eosinophil markers. Adjusted p -values from differential expression testing (Wilcoxon rank-sum test). (E) Heatmap of averaged expression of 154 degranulation pathway genes. Scale represents gene expression Z score.

Article Snippet: Siglec-8 APC , REA1045 , 2 , Eosinophil isolation buffer , 130-117-975 , Miltenyi.

Techniques: Gene Expression, Expressing, Marker, Quantitative Proteomics

Healthy eosinophils are heterogeneous and vary in expression of essential effector genes (A) UMAP of all eosinophils ( n = 24,538) colored by patient (left) condition (middle) and cluster (right). (B) UMAP of healthy eosinophils only (left) and bar plot of the fraction of healthy cells per cluster (right). (C) Heatmap of average expression of cluster markers (Padj <0.05, log2FC > 0.25). Scale represents gene expression Z score. (D) Top gene ontology biological process pathways enriched in each cluster (Padj <0.05). (E) Violin plots of expression of primary and secondary granule genes and HLA genes. p values were determined by the Kruskal-Wallace test. (F) Dot plot of top interferon-stimulated gene markers for cluster 3 colored by scaled average expression. Adjusted p value from Wilcoxon rank-sum test.

Journal: iScience

Article Title: Single-cell RNA-sequencing of circulating eosinophils from asthma patients reveals an inflammatory signature

doi: 10.1016/j.isci.2025.112609

Figure Lengend Snippet: Healthy eosinophils are heterogeneous and vary in expression of essential effector genes (A) UMAP of all eosinophils ( n = 24,538) colored by patient (left) condition (middle) and cluster (right). (B) UMAP of healthy eosinophils only (left) and bar plot of the fraction of healthy cells per cluster (right). (C) Heatmap of average expression of cluster markers (Padj <0.05, log2FC > 0.25). Scale represents gene expression Z score. (D) Top gene ontology biological process pathways enriched in each cluster (Padj <0.05). (E) Violin plots of expression of primary and secondary granule genes and HLA genes. p values were determined by the Kruskal-Wallace test. (F) Dot plot of top interferon-stimulated gene markers for cluster 3 colored by scaled average expression. Adjusted p value from Wilcoxon rank-sum test.

Article Snippet: Siglec-8 APC , REA1045 , 2 , Eosinophil isolation buffer , 130-117-975 , Miltenyi.

Techniques: Expressing, Gene Expression

Asthmatic eosinophils have distinct gene expression profiles from healthy eosinophils (A) UMAP plot of down sampled eosinophils from healthy and asthma patients colored by condition (left) and cluster (right). (B) Bar plot of fraction of cells per condition for each cluster. (C) Volcano plot of significant DEGs in healthy vs. asthmatic eosinophils (P adj < 0.05, log2FC > 0.25). The top 5 most significant genes per group are labeled. (D) Violin plots of expression of class I HLA genes, antigen presentation genes, granule genes and CCR3. Adjusted p value from Wilcoxon rank-sum test.

Journal: iScience

Article Title: Single-cell RNA-sequencing of circulating eosinophils from asthma patients reveals an inflammatory signature

doi: 10.1016/j.isci.2025.112609

Figure Lengend Snippet: Asthmatic eosinophils have distinct gene expression profiles from healthy eosinophils (A) UMAP plot of down sampled eosinophils from healthy and asthma patients colored by condition (left) and cluster (right). (B) Bar plot of fraction of cells per condition for each cluster. (C) Volcano plot of significant DEGs in healthy vs. asthmatic eosinophils (P adj < 0.05, log2FC > 0.25). The top 5 most significant genes per group are labeled. (D) Violin plots of expression of class I HLA genes, antigen presentation genes, granule genes and CCR3. Adjusted p value from Wilcoxon rank-sum test.

Article Snippet: Siglec-8 APC , REA1045 , 2 , Eosinophil isolation buffer , 130-117-975 , Miltenyi.

Techniques: Gene Expression, Labeling, Expressing, Immunopeptidomics

Asthmatic eosinophils exhibit an inflammatory gene signature (A) GSEA line plots of enriched hallmark pathways in asthma compared to healthy: hallmark interferon gamma response (left), hallmark interferon alpha response (middle), and hallmark inflammatory response (right). (B) Cord plot of 13 genes in the hallmark interferon gamma response, hallmark interferon alpha response, and hallmark inflammatory response pathways which are significantly overexpressed in asthmatic eosinophils compared to healthy.

Journal: iScience

Article Title: Single-cell RNA-sequencing of circulating eosinophils from asthma patients reveals an inflammatory signature

doi: 10.1016/j.isci.2025.112609

Figure Lengend Snippet: Asthmatic eosinophils exhibit an inflammatory gene signature (A) GSEA line plots of enriched hallmark pathways in asthma compared to healthy: hallmark interferon gamma response (left), hallmark interferon alpha response (middle), and hallmark inflammatory response (right). (B) Cord plot of 13 genes in the hallmark interferon gamma response, hallmark interferon alpha response, and hallmark inflammatory response pathways which are significantly overexpressed in asthmatic eosinophils compared to healthy.

Article Snippet: Siglec-8 APC , REA1045 , 2 , Eosinophil isolation buffer , 130-117-975 , Miltenyi.

Techniques:

Mild and severe asthmatic eosinophils have distinct gene expression profiles (A) UMAP clustering of all eosinophils colored by disease severity. (B) Bar plot of fraction of cells per condition for each cluster. (C) Volcano plot of significant DEGs between mild and severe asthmatic eosinophils (P adj < 0.05, log2FC > 0.25). The top 5 most significant genes per group are labeled.

Journal: iScience

Article Title: Single-cell RNA-sequencing of circulating eosinophils from asthma patients reveals an inflammatory signature

doi: 10.1016/j.isci.2025.112609

Figure Lengend Snippet: Mild and severe asthmatic eosinophils have distinct gene expression profiles (A) UMAP clustering of all eosinophils colored by disease severity. (B) Bar plot of fraction of cells per condition for each cluster. (C) Volcano plot of significant DEGs between mild and severe asthmatic eosinophils (P adj < 0.05, log2FC > 0.25). The top 5 most significant genes per group are labeled.

Article Snippet: Siglec-8 APC , REA1045 , 2 , Eosinophil isolation buffer , 130-117-975 , Miltenyi.

Techniques: Gene Expression, Labeling

Severe asthmatic eosinophils exhibit an inflammatory gene signature (A) Normalized enrichment scores (NES) from GSEA analysis of hallmark gene sets. A negative NES indicates the pathway is enriched in severe eosinophils, and a positive NES indicates the pathway is enriched in mild eosinophils. (B) GSEA line plot (left) and UMAP plot colored by activity score of enriched hallmark interferon alpha response genes (right). (C) GSEA line plot (left) and UMAP plot colored by activity score of enriched hallmark interferon gamma response genes. (D) Selected interferon-stimulated genes which are significantly overrepresented in severe asthmatic eosinophils compared to mild.

Journal: iScience

Article Title: Single-cell RNA-sequencing of circulating eosinophils from asthma patients reveals an inflammatory signature

doi: 10.1016/j.isci.2025.112609

Figure Lengend Snippet: Severe asthmatic eosinophils exhibit an inflammatory gene signature (A) Normalized enrichment scores (NES) from GSEA analysis of hallmark gene sets. A negative NES indicates the pathway is enriched in severe eosinophils, and a positive NES indicates the pathway is enriched in mild eosinophils. (B) GSEA line plot (left) and UMAP plot colored by activity score of enriched hallmark interferon alpha response genes (right). (C) GSEA line plot (left) and UMAP plot colored by activity score of enriched hallmark interferon gamma response genes. (D) Selected interferon-stimulated genes which are significantly overrepresented in severe asthmatic eosinophils compared to mild.

Article Snippet: Siglec-8 APC , REA1045 , 2 , Eosinophil isolation buffer , 130-117-975 , Miltenyi.

Techniques: Activity Assay

Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by HPLC. Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.

Journal: Journal of fungi (Basel, Switzerland)

Article Title: Suppression of Chitin-Triggered Immunity by a New Fungal Chitin-Binding Effector Resulting from Alternative Splicing of a Chitin Deacetylase Gene.

doi: 10.3390/jof8101022

Figure Lengend Snippet: Figure 4. Chitin-binding activity of His-tagged PxCDA3 on different chitin oligomers. For these assays, His-tagged proteins were maintained bound to nickel affinity columns and incubated with a mix of chitin oligomers (GlcNAc)1–7. After washing the columns and elution and denaturation of the proteins, the content of oligomers retained by the proteins was analysed. (A) Analysis of chitin oligomers by HPLC. Chromatograms corresponding to reference oligomers are shown in a box on the right. A representative chromatogram from three independent experiments is shown. The peaks corresponding to chitin pentamers and hexamers are indicated. (B) Analysis of chitin oligomers by H-ESI-MS. Representative chromatograms from three independent experiments are shown. The peaks corresponding to chitin pentamers, hexamers, and heptamers are indicated.

Article Snippet: Fungi 2022, 8, 1022 6 of 20 directly analysed using a Jasco high performance liquid chromatography (HPLC) system equipped with a Luna 5 μm NH2 100 Å column (250 × 4.6 mm) (Phenomenex, Madrid, Spain).

Techniques: Binding Assay, Activity Assay, Incubation