polyclonal rabbit antibody against gal 3  (Boster Bio)


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    Boster Bio polyclonal rabbit antibody against gal 3
    Polyclonal Rabbit Antibody Against Gal 3, supplied by Boster Bio, 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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    goat against rabbit cy3  (Boster Bio)


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    Boster Bio goat against rabbit cy3
    Goat Against Rabbit Cy3, supplied by Boster Bio, 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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    rabbit primary antibodies against collagen i  (Boster Bio)


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    Boster Bio rabbit primary antibodies against collagen i
    Rabbit Primary Antibodies Against Collagen I, supplied by Boster Bio, 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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    rabbit monoclonal antibody against slc24a2  (Boster Bio)


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    Boster Bio rabbit monoclonal antibody against slc24a2
    Rabbit Monoclonal Antibody Against Slc24a2, supplied by Boster Bio, 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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    rabbit against rat  (Boster Bio)


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    Boster Bio rabbit against rat
    Rabbit Against Rat, supplied by Boster Bio, 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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    rabbit polyclonal antibodies against cyp2e1  (Boster Bio)


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    Boster Bio rabbit polyclonal antibodies against cyp2e1
    Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on <t>cytochrome</t> <t>P450</t> <t>2E1</t> <t>(CYP2E1)</t> activity in liver microsomes from rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13), and liver microsomes were collected. After in vitro incubation with microsomes, the metabolic rate was expressed as the ratio of 6-OH-chlorzoxazone to chlorzoxazone and weighted by the control group. Data represent the mean ± S.D. of n = 10 rats. The asterisks above the bars indicate differences between groups.
    Rabbit Polyclonal Antibodies Against Cyp2e1, supplied by Boster Bio, 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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    1) Product Images from "New insights into the downregulation of cytochrome P450 2E1 via nuclear factor κB-dependent pathways in immune-mediated liver injury"

    Article Title: New insights into the downregulation of cytochrome P450 2E1 via nuclear factor κB-dependent pathways in immune-mediated liver injury

    Journal: Heliyon

    doi: 10.1016/j.heliyon.2023.e22641

    Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on cytochrome P450 2E1 (CYP2E1) activity in liver microsomes from rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13), and liver microsomes were collected. After in vitro incubation with microsomes, the metabolic rate was expressed as the ratio of 6-OH-chlorzoxazone to chlorzoxazone and weighted by the control group. Data represent the mean ± S.D. of n = 10 rats. The asterisks above the bars indicate differences between groups.
    Figure Legend Snippet: Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on cytochrome P450 2E1 (CYP2E1) activity in liver microsomes from rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13), and liver microsomes were collected. After in vitro incubation with microsomes, the metabolic rate was expressed as the ratio of 6-OH-chlorzoxazone to chlorzoxazone and weighted by the control group. Data represent the mean ± S.D. of n = 10 rats. The asterisks above the bars indicate differences between groups.

    Techniques Used: Activity Assay, In Vitro, Incubation

    Effects of PDTC treatment on the expression of PKC, CREB, P-CREB, CYP2E1, NF-κB, and IκBα in immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13). Liver proteins were extracted to determine the expression of PKC, CREB, P-CREB, CYP2E1, NF-κB, and IκBα. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by Western blot analysis using anti-PKC, anti-CREB, anti-P-CREB, anti-CYP2E1 anti–NF–κB and anti-IκBα antibodies. The results were normalised to the levels of GAPDH and β-tubulin. Western blotting images showing the protein expression of (A) PKC, (B) P-CREB, (C) CREB, (D) CYP2E1, (E) NF-κB, and (F) IκBα in the rat liver. Image Quant software was used to quantify expression. Data are expressed as the mean ± S.D. of three independent experiments (n = 3). The asterisks above the bars indicate differences between groups. Comparisons between groups were performed using one-way ANOVA followed by Tukey's test. Abbreviations: PDTC, ammonium pyrrolidine dithiocarbamate; PKC, protein kinase C; CREB, cAMP-response element binding protein, P-CREB, phospho-CREB; CYP2E1, cytochrome P450 2E1; NF-κB, nuclear factor κB; IκBα, an inhibitor of NF-κB subunit alpha; BCG, Bacillus Calmette–Guerin; SDS-PAGE, sodium dodecyl sulphate-polyacrylamide gel electrophoresis; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; ANOVA, analysis of variance.
    Figure Legend Snippet: Effects of PDTC treatment on the expression of PKC, CREB, P-CREB, CYP2E1, NF-κB, and IκBα in immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13). Liver proteins were extracted to determine the expression of PKC, CREB, P-CREB, CYP2E1, NF-κB, and IκBα. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by Western blot analysis using anti-PKC, anti-CREB, anti-P-CREB, anti-CYP2E1 anti–NF–κB and anti-IκBα antibodies. The results were normalised to the levels of GAPDH and β-tubulin. Western blotting images showing the protein expression of (A) PKC, (B) P-CREB, (C) CREB, (D) CYP2E1, (E) NF-κB, and (F) IκBα in the rat liver. Image Quant software was used to quantify expression. Data are expressed as the mean ± S.D. of three independent experiments (n = 3). The asterisks above the bars indicate differences between groups. Comparisons between groups were performed using one-way ANOVA followed by Tukey's test. Abbreviations: PDTC, ammonium pyrrolidine dithiocarbamate; PKC, protein kinase C; CREB, cAMP-response element binding protein, P-CREB, phospho-CREB; CYP2E1, cytochrome P450 2E1; NF-κB, nuclear factor κB; IκBα, an inhibitor of NF-κB subunit alpha; BCG, Bacillus Calmette–Guerin; SDS-PAGE, sodium dodecyl sulphate-polyacrylamide gel electrophoresis; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; ANOVA, analysis of variance.

    Techniques Used: Expressing, SDS Page, Western Blot, Software, Binding Assay, Polyacrylamide Gel Electrophoresis

    Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on CYP2E1 and CREB mRNA expression in rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13). (A) BCG-mediated immuno-stimulation decreases the expression of CYP2E1 ( P < 0.01); conversely, PDTC treatment gradually recovers the CYP2E1 expression profile, with the high-dose group recovering to a level similar to that of the control group ( P < 0.05). (B) Low, medium, and high doses of PDTC downregulate CREB expression, with the high-dose group showing the most significant difference ( P < 0.05) Data represent the mean ± S.D. of n = 10 rats. P- values above scatter charts indicate differences between groups. Comparisons between groups were performed using one-way ANOVA followed by Tukey's test.
    Figure Legend Snippet: Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on CYP2E1 and CREB mRNA expression in rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13). (A) BCG-mediated immuno-stimulation decreases the expression of CYP2E1 ( P < 0.01); conversely, PDTC treatment gradually recovers the CYP2E1 expression profile, with the high-dose group recovering to a level similar to that of the control group ( P < 0.05). (B) Low, medium, and high doses of PDTC downregulate CREB expression, with the high-dose group showing the most significant difference ( P < 0.05) Data represent the mean ± S.D. of n = 10 rats. P- values above scatter charts indicate differences between groups. Comparisons between groups were performed using one-way ANOVA followed by Tukey's test.

    Techniques Used: Expressing

    polyclonal antibody against rabbit igg hrp  (Boster Bio)


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    Boster Bio polyclonal antibody against rabbit igg hrp
    Polyclonal Antibody Against Rabbit Igg Hrp, supplied by Boster Bio, 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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    antibodies against rabbit mouse  (Boster Bio)


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    Boster Bio antibodies against rabbit mouse
    Antibodies Against Rabbit Mouse, supplied by Boster Bio, 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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    rabbit primary antibody against cd68  (Boster Bio)


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    Boster Bio rabbit primary antibody against cd68
    Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of <t>CD68</t> (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
    Rabbit Primary Antibody Against Cd68, supplied by Boster Bio, 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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    1) Product Images from "Oxymatrine blocks the NLRP3 inflammasome pathway, partly downregulating the inflammatory responses of M1 macrophages differentiated from THP-1 monocytes"

    Article Title: Oxymatrine blocks the NLRP3 inflammasome pathway, partly downregulating the inflammatory responses of M1 macrophages differentiated from THP-1 monocytes

    Journal: Biochemistry and Biophysics Reports

    doi: 10.1016/j.bbrep.2023.101482

    Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
    Figure Legend Snippet: Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Techniques Used: Immunofluorescence, Staining

    rabbit primary antibody against cd86  (Boster Bio)


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    Boster Bio rabbit primary antibody against cd86
    Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of <t>CD86</t> (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
    Rabbit Primary Antibody Against Cd86, supplied by Boster Bio, 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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    1) Product Images from "Oxymatrine blocks the NLRP3 inflammasome pathway, partly downregulating the inflammatory responses of M1 macrophages differentiated from THP-1 monocytes "

    Article Title: Oxymatrine blocks the NLRP3 inflammasome pathway, partly downregulating the inflammatory responses of M1 macrophages differentiated from THP-1 monocytes

    Journal: Biochemistry and Biophysics Reports

    doi: 10.1016/j.bbrep.2023.101482

    Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
    Figure Legend Snippet: Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Techniques Used: Immunofluorescence, Staining

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    Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on <t>cytochrome</t> <t>P450</t> <t>2E1</t> <t>(CYP2E1)</t> activity in liver microsomes from rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13), and liver microsomes were collected. After in vitro incubation with microsomes, the metabolic rate was expressed as the ratio of 6-OH-chlorzoxazone to chlorzoxazone and weighted by the control group. Data represent the mean ± S.D. of n = 10 rats. The asterisks above the bars indicate differences between groups.
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    Boster Bio rabbit primary antibody against cd68
    Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of <t>CD68</t> (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
    Rabbit Primary Antibody Against Cd68, supplied by Boster Bio, 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/rabbit primary antibody against cd68/product/Boster Bio
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit primary antibody against cd68 - by Bioz Stars, 2024-06
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    86
    Boster Bio rabbit primary antibody against cd86
    Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of <t>CD86</t> (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
    Rabbit Primary Antibody Against Cd86, supplied by Boster Bio, 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/rabbit primary antibody against cd86/product/Boster Bio
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit primary antibody against cd86 - by Bioz Stars, 2024-06
    86/100 stars
      Buy from Supplier

    Image Search Results


    Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on cytochrome P450 2E1 (CYP2E1) activity in liver microsomes from rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13), and liver microsomes were collected. After in vitro incubation with microsomes, the metabolic rate was expressed as the ratio of 6-OH-chlorzoxazone to chlorzoxazone and weighted by the control group. Data represent the mean ± S.D. of n = 10 rats. The asterisks above the bars indicate differences between groups.

    Journal: Heliyon

    Article Title: New insights into the downregulation of cytochrome P450 2E1 via nuclear factor κB-dependent pathways in immune-mediated liver injury

    doi: 10.1016/j.heliyon.2023.e22641

    Figure Lengend Snippet: Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on cytochrome P450 2E1 (CYP2E1) activity in liver microsomes from rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13), and liver microsomes were collected. After in vitro incubation with microsomes, the metabolic rate was expressed as the ratio of 6-OH-chlorzoxazone to chlorzoxazone and weighted by the control group. Data represent the mean ± S.D. of n = 10 rats. The asterisks above the bars indicate differences between groups.

    Article Snippet: Enzyme-linked immunosorbent assay (ELISA) kits for measuring the levels of rat tumour necrosis factor-alpha (TNF-α), interleukin (IL)-1β, phosphodiesterase (PDE4), and cAMP, BCA protein kit, the sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) preparation kit, as well as rabbit polyclonal antibodies against CYP2E1 (catalogue number: PB0186), PKC (catalogue number: PBM0401), CREB (catalogue number: PB0513), phospho-CREB (P-CREB, catalogue number: P00577), NF-κB (catalogue number: BA0610), glyceraldehyde-3-phosphate dehydrogenase (GAPDH; catalogue number: BA2913), and β-tubulin (catalogue number: A01857-1), were purchased from Wuhan Boster Biological Engineering Co. Ltd. (Hubei, China).

    Techniques: Activity Assay, In Vitro, Incubation

    Effects of PDTC treatment on the expression of PKC, CREB, P-CREB, CYP2E1, NF-κB, and IκBα in immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13). Liver proteins were extracted to determine the expression of PKC, CREB, P-CREB, CYP2E1, NF-κB, and IκBα. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by Western blot analysis using anti-PKC, anti-CREB, anti-P-CREB, anti-CYP2E1 anti–NF–κB and anti-IκBα antibodies. The results were normalised to the levels of GAPDH and β-tubulin. Western blotting images showing the protein expression of (A) PKC, (B) P-CREB, (C) CREB, (D) CYP2E1, (E) NF-κB, and (F) IκBα in the rat liver. Image Quant software was used to quantify expression. Data are expressed as the mean ± S.D. of three independent experiments (n = 3). The asterisks above the bars indicate differences between groups. Comparisons between groups were performed using one-way ANOVA followed by Tukey's test. Abbreviations: PDTC, ammonium pyrrolidine dithiocarbamate; PKC, protein kinase C; CREB, cAMP-response element binding protein, P-CREB, phospho-CREB; CYP2E1, cytochrome P450 2E1; NF-κB, nuclear factor κB; IκBα, an inhibitor of NF-κB subunit alpha; BCG, Bacillus Calmette–Guerin; SDS-PAGE, sodium dodecyl sulphate-polyacrylamide gel electrophoresis; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; ANOVA, analysis of variance.

    Journal: Heliyon

    Article Title: New insights into the downregulation of cytochrome P450 2E1 via nuclear factor κB-dependent pathways in immune-mediated liver injury

    doi: 10.1016/j.heliyon.2023.e22641

    Figure Lengend Snippet: Effects of PDTC treatment on the expression of PKC, CREB, P-CREB, CYP2E1, NF-κB, and IκBα in immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13). Liver proteins were extracted to determine the expression of PKC, CREB, P-CREB, CYP2E1, NF-κB, and IκBα. Equal amounts (30 μg) of protein were subjected to SDS-PAGE followed by Western blot analysis using anti-PKC, anti-CREB, anti-P-CREB, anti-CYP2E1 anti–NF–κB and anti-IκBα antibodies. The results were normalised to the levels of GAPDH and β-tubulin. Western blotting images showing the protein expression of (A) PKC, (B) P-CREB, (C) CREB, (D) CYP2E1, (E) NF-κB, and (F) IκBα in the rat liver. Image Quant software was used to quantify expression. Data are expressed as the mean ± S.D. of three independent experiments (n = 3). The asterisks above the bars indicate differences between groups. Comparisons between groups were performed using one-way ANOVA followed by Tukey's test. Abbreviations: PDTC, ammonium pyrrolidine dithiocarbamate; PKC, protein kinase C; CREB, cAMP-response element binding protein, P-CREB, phospho-CREB; CYP2E1, cytochrome P450 2E1; NF-κB, nuclear factor κB; IκBα, an inhibitor of NF-κB subunit alpha; BCG, Bacillus Calmette–Guerin; SDS-PAGE, sodium dodecyl sulphate-polyacrylamide gel electrophoresis; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; ANOVA, analysis of variance.

    Article Snippet: Enzyme-linked immunosorbent assay (ELISA) kits for measuring the levels of rat tumour necrosis factor-alpha (TNF-α), interleukin (IL)-1β, phosphodiesterase (PDE4), and cAMP, BCA protein kit, the sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) preparation kit, as well as rabbit polyclonal antibodies against CYP2E1 (catalogue number: PB0186), PKC (catalogue number: PBM0401), CREB (catalogue number: PB0513), phospho-CREB (P-CREB, catalogue number: P00577), NF-κB (catalogue number: BA0610), glyceraldehyde-3-phosphate dehydrogenase (GAPDH; catalogue number: BA2913), and β-tubulin (catalogue number: A01857-1), were purchased from Wuhan Boster Biological Engineering Co. Ltd. (Hubei, China).

    Techniques: Expressing, SDS Page, Western Blot, Software, Binding Assay, Polyacrylamide Gel Electrophoresis

    Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on CYP2E1 and CREB mRNA expression in rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13). (A) BCG-mediated immuno-stimulation decreases the expression of CYP2E1 ( P < 0.01); conversely, PDTC treatment gradually recovers the CYP2E1 expression profile, with the high-dose group recovering to a level similar to that of the control group ( P < 0.05). (B) Low, medium, and high doses of PDTC downregulate CREB expression, with the high-dose group showing the most significant difference ( P < 0.05) Data represent the mean ± S.D. of n = 10 rats. P- values above scatter charts indicate differences between groups. Comparisons between groups were performed using one-way ANOVA followed by Tukey's test.

    Journal: Heliyon

    Article Title: New insights into the downregulation of cytochrome P450 2E1 via nuclear factor κB-dependent pathways in immune-mediated liver injury

    doi: 10.1016/j.heliyon.2023.e22641

    Figure Lengend Snippet: Effects of ammonium pyrrolidine dithiocarbamate (PDTC) treatment on CYP2E1 and CREB mRNA expression in rats with immune-mediated liver injury. Rats were administered injections of BCG (125 mg/kg, i.v. on day 1) or BCG (125 mg/kg, i.v. on day 1) + PDTC (25, 50, or 100 mg/kg/d, i.p. on days 11, 12, and 13). (A) BCG-mediated immuno-stimulation decreases the expression of CYP2E1 ( P < 0.01); conversely, PDTC treatment gradually recovers the CYP2E1 expression profile, with the high-dose group recovering to a level similar to that of the control group ( P < 0.05). (B) Low, medium, and high doses of PDTC downregulate CREB expression, with the high-dose group showing the most significant difference ( P < 0.05) Data represent the mean ± S.D. of n = 10 rats. P- values above scatter charts indicate differences between groups. Comparisons between groups were performed using one-way ANOVA followed by Tukey's test.

    Article Snippet: Enzyme-linked immunosorbent assay (ELISA) kits for measuring the levels of rat tumour necrosis factor-alpha (TNF-α), interleukin (IL)-1β, phosphodiesterase (PDE4), and cAMP, BCA protein kit, the sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) preparation kit, as well as rabbit polyclonal antibodies against CYP2E1 (catalogue number: PB0186), PKC (catalogue number: PBM0401), CREB (catalogue number: PB0513), phospho-CREB (P-CREB, catalogue number: P00577), NF-κB (catalogue number: BA0610), glyceraldehyde-3-phosphate dehydrogenase (GAPDH; catalogue number: BA2913), and β-tubulin (catalogue number: A01857-1), were purchased from Wuhan Boster Biological Engineering Co. Ltd. (Hubei, China).

    Techniques: Expressing

    Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (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: Oxymatrine blocks the NLRP3 inflammasome pathway, partly downregulating the inflammatory responses of M1 macrophages differentiated from THP-1 monocytes

    doi: 10.1016/j.bbrep.2023.101482

    Figure Lengend Snippet: Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: For immunofluorescence staining, the cells were fixed with 4% paraformaldehyde (PFA) (Biosharp, Anhui, China) and incubated with diluted rabbit primary antibody against CD68 (1:300) (Boster, Wuhan, China) overnight at 4 °C.

    Techniques: Immunofluorescence, Staining

    Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (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: Oxymatrine blocks the NLRP3 inflammasome pathway, partly downregulating the inflammatory responses of M1 macrophages differentiated from THP-1 monocytes

    doi: 10.1016/j.bbrep.2023.101482

    Figure Lengend Snippet: Morphological images of cells in different states and identification of M0 and M1 macrophages. (A) Morphology of THP-1 cells, M0 macrophages, and M1 macrophages. Scale bar: 200 μm. THP-1 monocytes were round, translucent, and suspended; M0 macrophages were clustered and adherent; M1 macrophages were adherent and can extend pseudopodias. (B) Immunofluorescence staining on M0 cells. Scale bar: 50 μm. Colocalization of CD68 (red) and DAPI (blue). (C) Immunofluorescence staining of M1 cells. Scale bar: 50 μm. Colocalization of CD86 (red) and DAPI (blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: A rabbit primary antibody against CD86 (1:300) (Boster, Wuhan, China) was used to identify M1 cells using the protocol described in section .

    Techniques: Immunofluorescence, Staining