bovine hmgb 1  (Chondrex Inc)


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    Chondrex Inc bovine hmgb 1
    Intraperitoneal pretreatment with propionic acid ameliorates liver IRI in mice. (A) WT mice were divided into two groups. Mice in the PA group were intraperitoneally pretreated with PA (5 mmol/kg in saline) 2 h prior to liver ischemia, whereas mice in the saline group were pretreated with saline. Then, mice in both groups were performed liver IRI model. (B) The sALT level after 6 h of reperfusion (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (C) Macroscopic findings after 6 h of reperfusion in saline- and PA -pretreated mice. Regions (bleeding and swelling) of macroscopic changes induced by IR insult are circled by dotted lines. (D) Representative liver histology (H&E staining) after IR insult (magnification ×400). Congestion area was shown in circle by yellow dot. (E) Suzuki’s histological grading in each group (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (F) Quantitative RT-PCR detection of inflammatory cytokines (TNF-α, IL-6, CXCL-1, CXCL-2, IL-1β, and IL-10) at 6 h of reperfusion. Data were normalized to β-actin gene expression (n = 6 mice/group; *P < .05, **P < .01) (Power calculation: TNF-α; 0.998, IL-6; 0.980, CXCL-2; 1.000, IL-1β; 0.996). The reduction of CXCL-1 and IL-10 in PA-treated group compared to saline-treated group was not significant. (G) The levels of serum <t>HMGB-1</t> at 6 h after reperfusion in saline- and PA -pretreated mice (n = 8 mice/group; **P < .01) (Power calculation: 1.000).
    Bovine Hmgb 1, supplied by Chondrex Inc, 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/result/bovine hmgb 1/product/Chondrex Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    bovine hmgb 1 - by Bioz Stars, 2023-09
    86/100 stars

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    1) Product Images from "Propionic Acid, Induced in Gut by an Inulin Diet, Suppresses Inflammation and Ameliorates Liver Ischemia and Reperfusion Injury in Mice"

    Article Title: Propionic Acid, Induced in Gut by an Inulin Diet, Suppresses Inflammation and Ameliorates Liver Ischemia and Reperfusion Injury in Mice

    Journal: Frontiers in Immunology

    doi: 10.3389/fimmu.2022.862503

    Intraperitoneal pretreatment with propionic acid ameliorates liver IRI in mice. (A) WT mice were divided into two groups. Mice in the PA group were intraperitoneally pretreated with PA (5 mmol/kg in saline) 2 h prior to liver ischemia, whereas mice in the saline group were pretreated with saline. Then, mice in both groups were performed liver IRI model. (B) The sALT level after 6 h of reperfusion (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (C) Macroscopic findings after 6 h of reperfusion in saline- and PA -pretreated mice. Regions (bleeding and swelling) of macroscopic changes induced by IR insult are circled by dotted lines. (D) Representative liver histology (H&E staining) after IR insult (magnification ×400). Congestion area was shown in circle by yellow dot. (E) Suzuki’s histological grading in each group (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (F) Quantitative RT-PCR detection of inflammatory cytokines (TNF-α, IL-6, CXCL-1, CXCL-2, IL-1β, and IL-10) at 6 h of reperfusion. Data were normalized to β-actin gene expression (n = 6 mice/group; *P < .05, **P < .01) (Power calculation: TNF-α; 0.998, IL-6; 0.980, CXCL-2; 1.000, IL-1β; 0.996). The reduction of CXCL-1 and IL-10 in PA-treated group compared to saline-treated group was not significant. (G) The levels of serum HMGB-1 at 6 h after reperfusion in saline- and PA -pretreated mice (n = 8 mice/group; **P < .01) (Power calculation: 1.000).
    Figure Legend Snippet: Intraperitoneal pretreatment with propionic acid ameliorates liver IRI in mice. (A) WT mice were divided into two groups. Mice in the PA group were intraperitoneally pretreated with PA (5 mmol/kg in saline) 2 h prior to liver ischemia, whereas mice in the saline group were pretreated with saline. Then, mice in both groups were performed liver IRI model. (B) The sALT level after 6 h of reperfusion (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (C) Macroscopic findings after 6 h of reperfusion in saline- and PA -pretreated mice. Regions (bleeding and swelling) of macroscopic changes induced by IR insult are circled by dotted lines. (D) Representative liver histology (H&E staining) after IR insult (magnification ×400). Congestion area was shown in circle by yellow dot. (E) Suzuki’s histological grading in each group (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (F) Quantitative RT-PCR detection of inflammatory cytokines (TNF-α, IL-6, CXCL-1, CXCL-2, IL-1β, and IL-10) at 6 h of reperfusion. Data were normalized to β-actin gene expression (n = 6 mice/group; *P < .05, **P < .01) (Power calculation: TNF-α; 0.998, IL-6; 0.980, CXCL-2; 1.000, IL-1β; 0.996). The reduction of CXCL-1 and IL-10 in PA-treated group compared to saline-treated group was not significant. (G) The levels of serum HMGB-1 at 6 h after reperfusion in saline- and PA -pretreated mice (n = 8 mice/group; **P < .01) (Power calculation: 1.000).

    Techniques Used: Staining, Quantitative RT-PCR, Expressing

    PA suppressed HMGB-1-mediated activation of peritoneal macrophages. Peritoneal macrophages from WT mice stimulated by HMGB-1 (1 µg/mL) were cultured with or without the pretreatment with PA (1, 2, 5, and 10 mM, respectively) for 48 h. (A) TNF-α release was measured by ELISA (n = 3 samples/group; ****P < .0001) (Power calculation: 1.000). (B) Western blot assisted analyses of NF-κB signaling and MAPK signaling molecules in the macrophages stimulated by HMGB-1 (1 µg/mL) 30 min after the pretreatment with PA (5 mM). β-actin was used as the internal control.
    Figure Legend Snippet: PA suppressed HMGB-1-mediated activation of peritoneal macrophages. Peritoneal macrophages from WT mice stimulated by HMGB-1 (1 µg/mL) were cultured with or without the pretreatment with PA (1, 2, 5, and 10 mM, respectively) for 48 h. (A) TNF-α release was measured by ELISA (n = 3 samples/group; ****P < .0001) (Power calculation: 1.000). (B) Western blot assisted analyses of NF-κB signaling and MAPK signaling molecules in the macrophages stimulated by HMGB-1 (1 µg/mL) 30 min after the pretreatment with PA (5 mM). β-actin was used as the internal control.

    Techniques Used: Activation Assay, Cell Culture, Enzyme-linked Immunosorbent Assay, Western Blot

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    Chondrex Inc bovine hmgb 1
    Intraperitoneal pretreatment with propionic acid ameliorates liver IRI in mice. (A) WT mice were divided into two groups. Mice in the PA group were intraperitoneally pretreated with PA (5 mmol/kg in saline) 2 h prior to liver ischemia, whereas mice in the saline group were pretreated with saline. Then, mice in both groups were performed liver IRI model. (B) The sALT level after 6 h of reperfusion (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (C) Macroscopic findings after 6 h of reperfusion in saline- and PA -pretreated mice. Regions (bleeding and swelling) of macroscopic changes induced by IR insult are circled by dotted lines. (D) Representative liver histology (H&E staining) after IR insult (magnification ×400). Congestion area was shown in circle by yellow dot. (E) Suzuki’s histological grading in each group (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (F) Quantitative RT-PCR detection of inflammatory cytokines (TNF-α, IL-6, CXCL-1, CXCL-2, IL-1β, and IL-10) at 6 h of reperfusion. Data were normalized to β-actin gene expression (n = 6 mice/group; *P < .05, **P < .01) (Power calculation: TNF-α; 0.998, IL-6; 0.980, CXCL-2; 1.000, IL-1β; 0.996). The reduction of CXCL-1 and IL-10 in PA-treated group compared to saline-treated group was not significant. (G) The levels of serum <t>HMGB-1</t> at 6 h after reperfusion in saline- and PA -pretreated mice (n = 8 mice/group; **P < .01) (Power calculation: 1.000).
    Bovine Hmgb 1, supplied by Chondrex Inc, 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/result/bovine hmgb 1/product/Chondrex Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    bovine hmgb 1 - by Bioz Stars, 2023-09
    86/100 stars
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    Intraperitoneal pretreatment with propionic acid ameliorates liver IRI in mice. (A) WT mice were divided into two groups. Mice in the PA group were intraperitoneally pretreated with PA (5 mmol/kg in saline) 2 h prior to liver ischemia, whereas mice in the saline group were pretreated with saline. Then, mice in both groups were performed liver IRI model. (B) The sALT level after 6 h of reperfusion (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (C) Macroscopic findings after 6 h of reperfusion in saline- and PA -pretreated mice. Regions (bleeding and swelling) of macroscopic changes induced by IR insult are circled by dotted lines. (D) Representative liver histology (H&E staining) after IR insult (magnification ×400). Congestion area was shown in circle by yellow dot. (E) Suzuki’s histological grading in each group (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (F) Quantitative RT-PCR detection of inflammatory cytokines (TNF-α, IL-6, CXCL-1, CXCL-2, IL-1β, and IL-10) at 6 h of reperfusion. Data were normalized to β-actin gene expression (n = 6 mice/group; *P < .05, **P < .01) (Power calculation: TNF-α; 0.998, IL-6; 0.980, CXCL-2; 1.000, IL-1β; 0.996). The reduction of CXCL-1 and IL-10 in PA-treated group compared to saline-treated group was not significant. (G) The levels of serum HMGB-1 at 6 h after reperfusion in saline- and PA -pretreated mice (n = 8 mice/group; **P < .01) (Power calculation: 1.000).

    Journal: Frontiers in Immunology

    Article Title: Propionic Acid, Induced in Gut by an Inulin Diet, Suppresses Inflammation and Ameliorates Liver Ischemia and Reperfusion Injury in Mice

    doi: 10.3389/fimmu.2022.862503

    Figure Lengend Snippet: Intraperitoneal pretreatment with propionic acid ameliorates liver IRI in mice. (A) WT mice were divided into two groups. Mice in the PA group were intraperitoneally pretreated with PA (5 mmol/kg in saline) 2 h prior to liver ischemia, whereas mice in the saline group were pretreated with saline. Then, mice in both groups were performed liver IRI model. (B) The sALT level after 6 h of reperfusion (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (C) Macroscopic findings after 6 h of reperfusion in saline- and PA -pretreated mice. Regions (bleeding and swelling) of macroscopic changes induced by IR insult are circled by dotted lines. (D) Representative liver histology (H&E staining) after IR insult (magnification ×400). Congestion area was shown in circle by yellow dot. (E) Suzuki’s histological grading in each group (n = 8 mice/group; ****P < .0001) (Power calculation: 1.000). (F) Quantitative RT-PCR detection of inflammatory cytokines (TNF-α, IL-6, CXCL-1, CXCL-2, IL-1β, and IL-10) at 6 h of reperfusion. Data were normalized to β-actin gene expression (n = 6 mice/group; *P < .05, **P < .01) (Power calculation: TNF-α; 0.998, IL-6; 0.980, CXCL-2; 1.000, IL-1β; 0.996). The reduction of CXCL-1 and IL-10 in PA-treated group compared to saline-treated group was not significant. (G) The levels of serum HMGB-1 at 6 h after reperfusion in saline- and PA -pretreated mice (n = 8 mice/group; **P < .01) (Power calculation: 1.000).

    Article Snippet: Then, bovine HMGB-1 (Chondrex, Redmond, WA, USA) (1 µg/mL) was added to the macrophages.

    Techniques: Staining, Quantitative RT-PCR, Expressing

    PA suppressed HMGB-1-mediated activation of peritoneal macrophages. Peritoneal macrophages from WT mice stimulated by HMGB-1 (1 µg/mL) were cultured with or without the pretreatment with PA (1, 2, 5, and 10 mM, respectively) for 48 h. (A) TNF-α release was measured by ELISA (n = 3 samples/group; ****P < .0001) (Power calculation: 1.000). (B) Western blot assisted analyses of NF-κB signaling and MAPK signaling molecules in the macrophages stimulated by HMGB-1 (1 µg/mL) 30 min after the pretreatment with PA (5 mM). β-actin was used as the internal control.

    Journal: Frontiers in Immunology

    Article Title: Propionic Acid, Induced in Gut by an Inulin Diet, Suppresses Inflammation and Ameliorates Liver Ischemia and Reperfusion Injury in Mice

    doi: 10.3389/fimmu.2022.862503

    Figure Lengend Snippet: PA suppressed HMGB-1-mediated activation of peritoneal macrophages. Peritoneal macrophages from WT mice stimulated by HMGB-1 (1 µg/mL) were cultured with or without the pretreatment with PA (1, 2, 5, and 10 mM, respectively) for 48 h. (A) TNF-α release was measured by ELISA (n = 3 samples/group; ****P < .0001) (Power calculation: 1.000). (B) Western blot assisted analyses of NF-κB signaling and MAPK signaling molecules in the macrophages stimulated by HMGB-1 (1 µg/mL) 30 min after the pretreatment with PA (5 mM). β-actin was used as the internal control.

    Article Snippet: Then, bovine HMGB-1 (Chondrex, Redmond, WA, USA) (1 µg/mL) was added to the macrophages.

    Techniques: Activation Assay, Cell Culture, Enzyme-linked Immunosorbent Assay, Western Blot