il 6 mrna Search Results


il-6 mrna  (MacVector inc)
90
MacVector inc il-6 mrna
Il 6 Mrna, supplied by MacVector inc, 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/il+6+mrna/pm27793010-104-34-27?v=MacVector+inc
Average 90 stars, based on 1 article reviews
il-6 mrna - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
xplore human il-6 mrna assay  (Endogen Inc)
90
Endogen Inc xplore human il-6 mrna assay
Xplore Human Il 6 Mrna Assay, supplied by Endogen Inc, 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/il+6+mrna/pm11766126-93-6-15?v=Endogen+Inc
Average 90 stars, based on 1 article reviews
xplore human il-6 mrna assay - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
cox-2 mrna  (MolBio Diagnostics)
90
MolBio Diagnostics cox-2 mrna
Cox 2 Mrna, supplied by MolBio Diagnostics, 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/il+6+mrna/pmc00538736-408-17-10?v=MolBio+Diagnostics
Average 90 stars, based on 1 article reviews
cox-2 mrna - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
il-6 mrna fish probe (red)  (Ribobio co)
90
Ribobio co il-6 mrna fish probe (red)
Activation of circulating monocytes in monkeys with acute liver failure. A, ELISA measurement of serum levels of sCD 163 in the treated monkeys at indicated times; n = 7; *** P < .001. B, Representative photomicrographs of the results of immunohistochemical staining to identify resident KC s ( CD 68+) and recruited hepatic macrophages ( MAC 387+) in liver tissues. C, Quantitation of CD 68+ and MAC 387+ macrophages. The numbers of CD 68+ and MAC 387+ cells were counted in 10 consecutive high‐power fields in 3 monkeys. For each section, 10 randomly chosen portal tracts or areas of central veins were assessed at high magnification (×400), and the cumulative number of positive cells in 10 HPF was recorded. Data represent the means ± SEM ; n = 7; ** P < .01, *** P < .001. D, Double immunofluorescence staining for CD 68 and Ki67 in liver tissues. Note that the Ki67‐positive cells (indicated by arrowheads) are hepatocytes but not CD 68+ KC s (arrows). E, <t>FISH</t> assay for IL ‐6 <t>mRNA</t> in biopsy liver tissues at different time points. Macrophages are indicated by arrows identified by their shape, size and lobular location. F, Transcript levels of IL ‐6 in liver homogenates, circulating monocytes, and lymphocytes. Each bar represents data obtained from at least 3 independent quantitative PCR experiments. Data represent the means ± SEM ; n > 3; NS , not significant. *** P < .001. G, Flow cytometric analysis of activated monocytes ( CD 14+ CD 16+ CCR 2+) in subsets of peripheral blood monocyte. Data represent the means ± SEM ; n = 7; *** P < .001
Il 6 Mrna Fish Probe (Red), supplied by Ribobio co, 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/il+6+mrna/pmc06111866-75-0-7?v=Ribobio+co
Average 90 stars, based on 1 article reviews
il-6 mrna fish probe (red) - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
il-6, il-8 protein and mrna  (Millar Inc)
90
Millar Inc il-6, il-8 protein and mrna
Activation of circulating monocytes in monkeys with acute liver failure. A, ELISA measurement of serum levels of sCD 163 in the treated monkeys at indicated times; n = 7; *** P < .001. B, Representative photomicrographs of the results of immunohistochemical staining to identify resident KC s ( CD 68+) and recruited hepatic macrophages ( MAC 387+) in liver tissues. C, Quantitation of CD 68+ and MAC 387+ macrophages. The numbers of CD 68+ and MAC 387+ cells were counted in 10 consecutive high‐power fields in 3 monkeys. For each section, 10 randomly chosen portal tracts or areas of central veins were assessed at high magnification (×400), and the cumulative number of positive cells in 10 HPF was recorded. Data represent the means ± SEM ; n = 7; ** P < .01, *** P < .001. D, Double immunofluorescence staining for CD 68 and Ki67 in liver tissues. Note that the Ki67‐positive cells (indicated by arrowheads) are hepatocytes but not CD 68+ KC s (arrows). E, <t>FISH</t> assay for IL ‐6 <t>mRNA</t> in biopsy liver tissues at different time points. Macrophages are indicated by arrows identified by their shape, size and lobular location. F, Transcript levels of IL ‐6 in liver homogenates, circulating monocytes, and lymphocytes. Each bar represents data obtained from at least 3 independent quantitative PCR experiments. Data represent the means ± SEM ; n > 3; NS , not significant. *** P < .001. G, Flow cytometric analysis of activated monocytes ( CD 14+ CD 16+ CCR 2+) in subsets of peripheral blood monocyte. Data represent the means ± SEM ; n = 7; *** P < .001
Il 6, Il 8 Protein And Mrna, supplied by Millar Inc, 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/il+6+mrna/pmc07006114-9-38-0?v=Millar+Inc
Average 90 stars, based on 1 article reviews
il-6, il-8 protein and mrna - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
il 6 mrna  (Genechem)
86
Genechem il 6 mrna
Activation of circulating monocytes in monkeys with acute liver failure. A, ELISA measurement of serum levels of sCD 163 in the treated monkeys at indicated times; n = 7; *** P < .001. B, Representative photomicrographs of the results of immunohistochemical staining to identify resident KC s ( CD 68+) and recruited hepatic macrophages ( MAC 387+) in liver tissues. C, Quantitation of CD 68+ and MAC 387+ macrophages. The numbers of CD 68+ and MAC 387+ cells were counted in 10 consecutive high‐power fields in 3 monkeys. For each section, 10 randomly chosen portal tracts or areas of central veins were assessed at high magnification (×400), and the cumulative number of positive cells in 10 HPF was recorded. Data represent the means ± SEM ; n = 7; ** P < .01, *** P < .001. D, Double immunofluorescence staining for CD 68 and Ki67 in liver tissues. Note that the Ki67‐positive cells (indicated by arrowheads) are hepatocytes but not CD 68+ KC s (arrows). E, <t>FISH</t> assay for IL ‐6 <t>mRNA</t> in biopsy liver tissues at different time points. Macrophages are indicated by arrows identified by their shape, size and lobular location. F, Transcript levels of IL ‐6 in liver homogenates, circulating monocytes, and lymphocytes. Each bar represents data obtained from at least 3 independent quantitative PCR experiments. Data represent the means ± SEM ; n > 3; NS , not significant. *** P < .001. G, Flow cytometric analysis of activated monocytes ( CD 14+ CD 16+ CCR 2+) in subsets of peripheral blood monocyte. Data represent the means ± SEM ; n = 7; *** P < .001
Il 6 Mrna, supplied by Genechem, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/il+6+mrna/pm41200189-108-12-18?v=Genechem
Average 86 stars, based on 1 article reviews
il 6 mrna - by Bioz Stars, 2026-07
86/100 stars
  Buy from Supplier
il-6 mrna expression  (Knoell Germany)
90
Knoell Germany il-6 mrna expression
Activation of circulating monocytes in monkeys with acute liver failure. A, ELISA measurement of serum levels of sCD 163 in the treated monkeys at indicated times; n = 7; *** P < .001. B, Representative photomicrographs of the results of immunohistochemical staining to identify resident KC s ( CD 68+) and recruited hepatic macrophages ( MAC 387+) in liver tissues. C, Quantitation of CD 68+ and MAC 387+ macrophages. The numbers of CD 68+ and MAC 387+ cells were counted in 10 consecutive high‐power fields in 3 monkeys. For each section, 10 randomly chosen portal tracts or areas of central veins were assessed at high magnification (×400), and the cumulative number of positive cells in 10 HPF was recorded. Data represent the means ± SEM ; n = 7; ** P < .01, *** P < .001. D, Double immunofluorescence staining for CD 68 and Ki67 in liver tissues. Note that the Ki67‐positive cells (indicated by arrowheads) are hepatocytes but not CD 68+ KC s (arrows). E, <t>FISH</t> assay for IL ‐6 <t>mRNA</t> in biopsy liver tissues at different time points. Macrophages are indicated by arrows identified by their shape, size and lobular location. F, Transcript levels of IL ‐6 in liver homogenates, circulating monocytes, and lymphocytes. Each bar represents data obtained from at least 3 independent quantitative PCR experiments. Data represent the means ± SEM ; n > 3; NS , not significant. *** P < .001. G, Flow cytometric analysis of activated monocytes ( CD 14+ CD 16+ CCR 2+) in subsets of peripheral blood monocyte. Data represent the means ± SEM ; n = 7; *** P < .001
Il 6 Mrna Expression, supplied by Knoell Germany, 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/il+6+mrna/pm36536187-75-28-21?v=Knoell+Germany
Average 90 stars, based on 1 article reviews
il-6 mrna expression - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
il-6 mrna  (TriLink)
90
TriLink il-6 mrna
Activation of circulating monocytes in monkeys with acute liver failure. A, ELISA measurement of serum levels of sCD 163 in the treated monkeys at indicated times; n = 7; *** P < .001. B, Representative photomicrographs of the results of immunohistochemical staining to identify resident KC s ( CD 68+) and recruited hepatic macrophages ( MAC 387+) in liver tissues. C, Quantitation of CD 68+ and MAC 387+ macrophages. The numbers of CD 68+ and MAC 387+ cells were counted in 10 consecutive high‐power fields in 3 monkeys. For each section, 10 randomly chosen portal tracts or areas of central veins were assessed at high magnification (×400), and the cumulative number of positive cells in 10 HPF was recorded. Data represent the means ± SEM ; n = 7; ** P < .01, *** P < .001. D, Double immunofluorescence staining for CD 68 and Ki67 in liver tissues. Note that the Ki67‐positive cells (indicated by arrowheads) are hepatocytes but not CD 68+ KC s (arrows). E, <t>FISH</t> assay for IL ‐6 <t>mRNA</t> in biopsy liver tissues at different time points. Macrophages are indicated by arrows identified by their shape, size and lobular location. F, Transcript levels of IL ‐6 in liver homogenates, circulating monocytes, and lymphocytes. Each bar represents data obtained from at least 3 independent quantitative PCR experiments. Data represent the means ± SEM ; n > 3; NS , not significant. *** P < .001. G, Flow cytometric analysis of activated monocytes ( CD 14+ CD 16+ CCR 2+) in subsets of peripheral blood monocyte. Data represent the means ± SEM ; n = 7; *** P < .001
Il 6 Mrna, supplied by TriLink, 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/il+6+mrna/pm34890489-50-0-5?v=TriLink
Average 90 stars, based on 1 article reviews
il-6 mrna - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


Activation of circulating monocytes in monkeys with acute liver failure. A, ELISA measurement of serum levels of sCD 163 in the treated monkeys at indicated times; n = 7; *** P < .001. B, Representative photomicrographs of the results of immunohistochemical staining to identify resident KC s ( CD 68+) and recruited hepatic macrophages ( MAC 387+) in liver tissues. C, Quantitation of CD 68+ and MAC 387+ macrophages. The numbers of CD 68+ and MAC 387+ cells were counted in 10 consecutive high‐power fields in 3 monkeys. For each section, 10 randomly chosen portal tracts or areas of central veins were assessed at high magnification (×400), and the cumulative number of positive cells in 10 HPF was recorded. Data represent the means ± SEM ; n = 7; ** P < .01, *** P < .001. D, Double immunofluorescence staining for CD 68 and Ki67 in liver tissues. Note that the Ki67‐positive cells (indicated by arrowheads) are hepatocytes but not CD 68+ KC s (arrows). E, FISH assay for IL ‐6 mRNA in biopsy liver tissues at different time points. Macrophages are indicated by arrows identified by their shape, size and lobular location. F, Transcript levels of IL ‐6 in liver homogenates, circulating monocytes, and lymphocytes. Each bar represents data obtained from at least 3 independent quantitative PCR experiments. Data represent the means ± SEM ; n > 3; NS , not significant. *** P < .001. G, Flow cytometric analysis of activated monocytes ( CD 14+ CD 16+ CCR 2+) in subsets of peripheral blood monocyte. Data represent the means ± SEM ; n = 7; *** P < .001

Journal: Journal of Cellular and Molecular Medicine

Article Title: Circulating monocytes accelerate acute liver failure by IL ‐6 secretion in monkey

doi: 10.1111/jcmm.13673

Figure Lengend Snippet: Activation of circulating monocytes in monkeys with acute liver failure. A, ELISA measurement of serum levels of sCD 163 in the treated monkeys at indicated times; n = 7; *** P < .001. B, Representative photomicrographs of the results of immunohistochemical staining to identify resident KC s ( CD 68+) and recruited hepatic macrophages ( MAC 387+) in liver tissues. C, Quantitation of CD 68+ and MAC 387+ macrophages. The numbers of CD 68+ and MAC 387+ cells were counted in 10 consecutive high‐power fields in 3 monkeys. For each section, 10 randomly chosen portal tracts or areas of central veins were assessed at high magnification (×400), and the cumulative number of positive cells in 10 HPF was recorded. Data represent the means ± SEM ; n = 7; ** P < .01, *** P < .001. D, Double immunofluorescence staining for CD 68 and Ki67 in liver tissues. Note that the Ki67‐positive cells (indicated by arrowheads) are hepatocytes but not CD 68+ KC s (arrows). E, FISH assay for IL ‐6 mRNA in biopsy liver tissues at different time points. Macrophages are indicated by arrows identified by their shape, size and lobular location. F, Transcript levels of IL ‐6 in liver homogenates, circulating monocytes, and lymphocytes. Each bar represents data obtained from at least 3 independent quantitative PCR experiments. Data represent the means ± SEM ; n > 3; NS , not significant. *** P < .001. G, Flow cytometric analysis of activated monocytes ( CD 14+ CD 16+ CCR 2+) in subsets of peripheral blood monocyte. Data represent the means ± SEM ; n = 7; *** P < .001

Article Snippet: IL‐6 mRNA FISH Probe (Red), synthesized by Ribobio (Guangzhou, China), was hybridized at 40°C for overnight.

Techniques: Activation Assay, Enzyme-linked Immunosorbent Assay, Immunohistochemical staining, Staining, Quantitation Assay, Double Immunofluorescence Staining, Real-time Polymerase Chain Reaction