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97
MedChemExpress carboxyfluorescein succinimidyl ester
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Beyotime cfda se fluorescent probe
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Bio-Rad cytoplasm
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Beyotime tracking kit
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Biotium cmfda
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Lumiprobe carboxyfluorescein succinimidyl ester cfda se dye lumitrace cfda se kit lumiprobe moscow russia
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Carboxyfluorescein Succinimidyl Ester Cfda Se Dye Lumitrace Cfda Se Kit Lumiprobe Moscow Russia, supplied by Lumiprobe, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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STEMCELL Technologies Inc 5 (6)- carboxyfluorescein diacetate n- succinimidyl ester (cfda- se)
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
5 (6) Carboxyfluorescein Diacetate N Succinimidyl Ester (Cfda Se), supplied by STEMCELL Technologies 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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STEMCELL Technologies Inc flashtag cfda-se
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Becton Dickinson cfda-se
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Cfda Se, supplied by Becton Dickinson, 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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Michael Bauer International cfda-se
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Federation of European Neuroscience Societies cfda/se staining
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Becton Dickinson carboxy-fluorescein diacetate, succinimidyl eater (cfse
CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and <t>CFSE-positive</t> cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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Image Search Results


CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and CFSE-positive cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Journal: Biochemistry and Biophysics Reports

Article Title: Alterations of the gut microbial community structure modulates the Th17 cells response in a rat model of asphyxial cardiac arrest

doi: 10.1016/j.bbrep.2023.101543

Figure Lengend Snippet: CA/CPR injury induced the Th17 cells response. (A) Th17 cells (CD4 was marked with green and IL-17 was marked with red) were present in the cortex of CA/CPR rat but was absent in the cortex of sham rat after 72 h following CA/CPR. (B) The level of IL-17, IL-6, and TNF-α increased in the serum of rats after 72 h following CA/CPR, compared with the rat in sham group. (C) The proportions of the Th17 cells in the PBMC were evidently enhanced from 1.71 ± 0.67% in the rats of sham group to 4.5 ± 1.2% in rats of CA/CPR group. (D)Th17 cells fluorescently labeled after microinjection in PPs were detected in the PBMC after 72 h following CA/CPR, and CFSE-positive cells derived from labeled PPs of small intestine accounted for 28.33 ± 6.18% of total Th17 cells (* P < 0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: The lymphocytes in the small intestines PPs of rats were labeled with carboxyfluorescein succinimidyl ester (CFSE, MedChemExpress, USA) by microinjection (25 μM in 2 ul of PBS per PP) after 24 h following CA/CPR.

Techniques: Labeling, Microinjection, Derivative Assay