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rabbit anti ho1  (Proteintech)


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    Structured Review

    Proteintech rabbit anti ho1
    Rabbit Anti Ho1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1892 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+ho1/HO-1%2FHMOX1+Antibody/pm41894401-103-7-11
    Average 96 stars, based on 1892 article reviews
    rabbit anti ho1 - by Bioz Stars, 2026-10
    96/100 stars

    Images

    Related Articles

    Immunofluorescence:

    Article Title: Sirt6 overexpression relieves ferroptosis and delays the progression of diabetic nephropathy via Nrf2/GPX4 pathway
    Article Snippet: .. Immunofluorescence assay Podocytes grown on cover slides were fixed with 4% formaldehyde for 30 min at room temperature, permeabilized 10 min with PbS containing 0.1% triton X-100, blocked for 10% fetal calf serum for 30 min at 37 °C. the samples were incubated with rabbit anti-Sirt6 polyclonal antibody (1:100, 13572-1-aP, Proteintech, Wuhan, China), rabbit anti-Nrf2 (1:50, 16396-1-aP, Proteintech), mouse anti-GPX4 (1:100, 67763-1-Ig, Proteintech), rabbit anti-Sod2 (1:50, 24127-1-aP, Proteintech), rabbit anti-Ho1 (1:200, 10701-1-aP, Proteintech) overnight at 4 °C, and then incubated with goat anti-rabbit or goat anti-mouse IgG H&L secondary antibody at 37 °C for 2h. .. Finally, cells were stained with daPI (Southernbiotech, uSa) for 5 min.

    Incubation:

    Article Title: Sirt6 overexpression relieves ferroptosis and delays the progression of diabetic nephropathy via Nrf2/GPX4 pathway
    Article Snippet: .. Immunofluorescence assay Podocytes grown on cover slides were fixed with 4% formaldehyde for 30 min at room temperature, permeabilized 10 min with PbS containing 0.1% triton X-100, blocked for 10% fetal calf serum for 30 min at 37 °C. the samples were incubated with rabbit anti-Sirt6 polyclonal antibody (1:100, 13572-1-aP, Proteintech, Wuhan, China), rabbit anti-Nrf2 (1:50, 16396-1-aP, Proteintech), mouse anti-GPX4 (1:100, 67763-1-Ig, Proteintech), rabbit anti-Sod2 (1:50, 24127-1-aP, Proteintech), rabbit anti-Ho1 (1:200, 10701-1-aP, Proteintech) overnight at 4 °C, and then incubated with goat anti-rabbit or goat anti-mouse IgG H&L secondary antibody at 37 °C for 2h. .. Finally, cells were stained with daPI (Southernbiotech, uSa) for 5 min.

    Article Title: Identification of autophagy-related key biomarkers in caerulein induced acute pancreatitis: In silico and in vivo study
    Article Snippet: .. The rabbit anti-Calpastatin (12250–1-AP, Proteintech, WuHan, China), rabbit anti-Ho1 (10701–1-AP, Proteintech, WuHan, China), rabbit anti-Sestrin2 (10795–1-AP, Proteintech, WuHan, China), rabbit anti-Npc1 (13926–1-AP, Proteintech, WuHan, China), rabbit anti-Nfe2l2 (16396–1-AP, Proteintech, WuHan, China), rabbit anti-P21, mouse anti-Kras (sc-30, Santa Cruz, CA, USA) and mouse anti-β-actin (sc-47778, Santa Cruz, CA, USA) were used separately in Tris buffered physiological saline (TBST) overnight at 4°C and incubated with the corresponding secondary antibodies for 1h the next day. ..

    Article Title: Identification of autophagy-related key biomarkers in caerulein induced acute pancreatitis: In silico and in vivo study.
    Article Snippet: .. The rabbit anti-Calpastatin (12250–1-AP, Proteintech, WuHan, China), rabbit anti-Ho1 (10701– 1-AP, Proteintech, WuHan, China), rabbit anti-Sestrin2 (10795–1-AP, Proteintech, WuHan, China), rabbit anti-Npc1 (13926– 1-AP, Proteintech, WuHan, China), rabbit anti-Nfe2l2 (16396–1-AP, Proteintech, WuHan, China), rabbit anti-P21, mouse anti-Kras (sc-30, Santa Cruz, CA, USA) and mouse anti-β-actin (sc-47778, Santa Cruz, CA, USA) were used separately in Tris buffered physiological saline (TBST) overnight at 4°C and incubated with the corresponding secondary antibodies for 1h the next day. ..

    Article Title: Sirt6 overexpression relieves ferroptosis and delays the progression of diabetic nephropathy via Nrf2/GPX4 pathway
    Article Snippet: .. The samples were incubated with rabbit anti-Sirt6 polyclonal antibody (1:100, 13572-1-AP, Proteintech, Wuhan, China), rabbit anti-Nrf2 (1:50, 16396-1-AP, Proteintech), mouse anti-GPX4 (1:100, 67763-1-Ig, Proteintech), rabbit anti-SOD2 (1:50, 24127-1-AP, Proteintech), rabbit anti-HO1 (1:200, 10701-1-AP, Proteintech) overnight at 4 °C, and then incubated with goat anti-rabbit or goat anti-mouse IgG H&L secondary antibody at 37 °C for 2h. .. Finally, cells were stained with DAPI (SouthernBiotech, USA) for 5 min.

    Saline:

    Article Title: Identification of autophagy-related key biomarkers in caerulein induced acute pancreatitis: In silico and in vivo study
    Article Snippet: .. The rabbit anti-Calpastatin (12250–1-AP, Proteintech, WuHan, China), rabbit anti-Ho1 (10701–1-AP, Proteintech, WuHan, China), rabbit anti-Sestrin2 (10795–1-AP, Proteintech, WuHan, China), rabbit anti-Npc1 (13926–1-AP, Proteintech, WuHan, China), rabbit anti-Nfe2l2 (16396–1-AP, Proteintech, WuHan, China), rabbit anti-P21, mouse anti-Kras (sc-30, Santa Cruz, CA, USA) and mouse anti-β-actin (sc-47778, Santa Cruz, CA, USA) were used separately in Tris buffered physiological saline (TBST) overnight at 4°C and incubated with the corresponding secondary antibodies for 1h the next day. ..

    Article Title: Identification of autophagy-related key biomarkers in caerulein induced acute pancreatitis: In silico and in vivo study.
    Article Snippet: .. The rabbit anti-Calpastatin (12250–1-AP, Proteintech, WuHan, China), rabbit anti-Ho1 (10701– 1-AP, Proteintech, WuHan, China), rabbit anti-Sestrin2 (10795–1-AP, Proteintech, WuHan, China), rabbit anti-Npc1 (13926– 1-AP, Proteintech, WuHan, China), rabbit anti-Nfe2l2 (16396–1-AP, Proteintech, WuHan, China), rabbit anti-P21, mouse anti-Kras (sc-30, Santa Cruz, CA, USA) and mouse anti-β-actin (sc-47778, Santa Cruz, CA, USA) were used separately in Tris buffered physiological saline (TBST) overnight at 4°C and incubated with the corresponding secondary antibodies for 1h the next day. ..



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    Oxidative stress and inflammation level increased in the hippocampus in COPD-related depression in rat model. (A) The antioxidant protein expression images of rat hippocampus. (B-D) Qualitative analysis of Nrf2, <t>HO1</t> and NQO1. (E) The Bcl2/Bax expression images of rat hippocampus. (F) Qualitative analysis of Bcl2/Bax. (G,H) qualitative analysis of p-NFκB and TNF-α. (I) The p-NFκB and TNF-α protein expression images of rat hippocampus. Data are presented as mean ± SEM, n=3. All statistical tests were conducted using two-way ANOVA. *, P<0.05, **, P<0.01, ***, P<0.001. ANOVA, analysis of variance; COPD, chronic obstructive pulmonary disease; CS, cigarette smoke; CTL, control; HO1, heme-oxygenase-1; NQO1, quinone oxidoreductase 1; Nrf2, nuclear factor erythroid 2-related factor 2; OVX, ovariectomy; p-NFκB, phosphorylated nuclear factor kappa B; SEM, standard error of the mean; TNF-α, tumor necrosis factor α.
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    Oxidative stress and inflammation level increased in the hippocampus in COPD-related depression in rat model. (A) The antioxidant protein expression images of rat hippocampus. (B-D) Qualitative analysis of Nrf2, <t>HO1</t> and NQO1. (E) The Bcl2/Bax expression images of rat hippocampus. (F) Qualitative analysis of Bcl2/Bax. (G,H) qualitative analysis of p-NFκB and TNF-α. (I) The p-NFκB and TNF-α protein expression images of rat hippocampus. Data are presented as mean ± SEM, n=3. All statistical tests were conducted using two-way ANOVA. *, P<0.05, **, P<0.01, ***, P<0.001. ANOVA, analysis of variance; COPD, chronic obstructive pulmonary disease; CS, cigarette smoke; CTL, control; HO1, heme-oxygenase-1; NQO1, quinone oxidoreductase 1; Nrf2, nuclear factor erythroid 2-related factor 2; OVX, ovariectomy; p-NFκB, phosphorylated nuclear factor kappa B; SEM, standard error of the mean; TNF-α, tumor necrosis factor α.
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    Oxidative stress and inflammation level increased in the hippocampus in COPD-related depression in rat model. (A) The antioxidant protein expression images of rat hippocampus. (B-D) Qualitative analysis of Nrf2, <t>HO1</t> and NQO1. (E) The Bcl2/Bax expression images of rat hippocampus. (F) Qualitative analysis of Bcl2/Bax. (G,H) qualitative analysis of p-NFκB and TNF-α. (I) The p-NFκB and TNF-α protein expression images of rat hippocampus. Data are presented as mean ± SEM, n=3. All statistical tests were conducted using two-way ANOVA. *, P<0.05, **, P<0.01, ***, P<0.001. ANOVA, analysis of variance; COPD, chronic obstructive pulmonary disease; CS, cigarette smoke; CTL, control; HO1, heme-oxygenase-1; NQO1, quinone oxidoreductase 1; Nrf2, nuclear factor erythroid 2-related factor 2; OVX, ovariectomy; p-NFκB, phosphorylated nuclear factor kappa B; SEM, standard error of the mean; TNF-α, tumor necrosis factor α.
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    Image Search Results


    Oxidative stress and inflammation level increased in the hippocampus in COPD-related depression in rat model. (A) The antioxidant protein expression images of rat hippocampus. (B-D) Qualitative analysis of Nrf2, HO1 and NQO1. (E) The Bcl2/Bax expression images of rat hippocampus. (F) Qualitative analysis of Bcl2/Bax. (G,H) qualitative analysis of p-NFκB and TNF-α. (I) The p-NFκB and TNF-α protein expression images of rat hippocampus. Data are presented as mean ± SEM, n=3. All statistical tests were conducted using two-way ANOVA. *, P<0.05, **, P<0.01, ***, P<0.001. ANOVA, analysis of variance; COPD, chronic obstructive pulmonary disease; CS, cigarette smoke; CTL, control; HO1, heme-oxygenase-1; NQO1, quinone oxidoreductase 1; Nrf2, nuclear factor erythroid 2-related factor 2; OVX, ovariectomy; p-NFκB, phosphorylated nuclear factor kappa B; SEM, standard error of the mean; TNF-α, tumor necrosis factor α.

    Journal: Journal of Thoracic Disease

    Article Title: Protective effects of estradiol on neuroinflammation in chronic obstructive pulmonary disease related depression

    doi: 10.21037/jtd-2025-247

    Figure Lengend Snippet: Oxidative stress and inflammation level increased in the hippocampus in COPD-related depression in rat model. (A) The antioxidant protein expression images of rat hippocampus. (B-D) Qualitative analysis of Nrf2, HO1 and NQO1. (E) The Bcl2/Bax expression images of rat hippocampus. (F) Qualitative analysis of Bcl2/Bax. (G,H) qualitative analysis of p-NFκB and TNF-α. (I) The p-NFκB and TNF-α protein expression images of rat hippocampus. Data are presented as mean ± SEM, n=3. All statistical tests were conducted using two-way ANOVA. *, P<0.05, **, P<0.01, ***, P<0.001. ANOVA, analysis of variance; COPD, chronic obstructive pulmonary disease; CS, cigarette smoke; CTL, control; HO1, heme-oxygenase-1; NQO1, quinone oxidoreductase 1; Nrf2, nuclear factor erythroid 2-related factor 2; OVX, ovariectomy; p-NFκB, phosphorylated nuclear factor kappa B; SEM, standard error of the mean; TNF-α, tumor necrosis factor α.

    Article Snippet: The membranes were blocked with 5% non-fat milk in TBST (Tris-buffered saline, 0.1% Tween 20) and then incubated overnight at 4 °C with primary antibodies: β-actin (1:20,000, Proteintech, #66009-1-Ig), nuclear factor erythroid 2-related factor-2 (Nrf2) (1:1,000, Proteintech, #80593-1), quinone oxidoreductase 1 (NQO1) (1:1,000, ABclonal, #A19586), heme-oxygenase-1 (HO1) (1:1,000, ABclonal, #A19062), phosphorylated nuclear factor kappa B (p-NFκB) (1:1,000, CST, #3033S), NFκB(1:1000, CST, #8242S), extracellular signal-regulated kinase 1/2 (ERK1/2) (1:1,000, Cell Signaling Technology, #4695), Phospho-ERK1/2 (1:2,000, Cell Signaling Technology, #4370), c-Jun-N-terminal kinase (JNK) (1:1,000, Cell Signaling Technology, #9252), Phospho-JNK (1:1,000, Cell Signaling Technology, #4668), Phospho-p38 (1:1,000, Cell Signaling Technology, #4511), p38 (1:1,000, Cell Signaling Technology, #9212), tumor necrosis factor α (TNF-α) (1:1,000, ABclonal, #A0277), inducible nitric oxide synthase (iNOS) (1:1,000, ImmunoWay, #YT3169), CD163 (1:1,000, ABclonal, #A8383), and CD86 (1:1,000, ABclonal, #A1199).

    Techniques: Expressing, Control

    E2 promotes BV2 cell MAPKs activation and M1 polarization . (A) WB images of anti-oxidative stress protein level in BV2 cells stimulated with LPS and/or E2. (B-D) qualitative analysis of Nrf2, HO-1 and NQO1. (E) WB images of BV2 cells polarization stimulated with LPS and/or E2. (F,G) Qualitative analysis of CD163 and iNOS. (H) WB images of MAPK signaling pathway protein level in BV2 cells stimulated with LPS and/or E2. (I-K) Qualitative analysis of p-JNK, p-ERK1/2, p-p38. Data are presented as mean ± SEM, n=3. All statistical tests were conducted using two-way ANOVA. *, P<0.05, **, P<0.01, ***, P<0.001. ANOVA, analysis of variance; CTL, control; E2, estradiol; HO1, heme-oxygenase-1; iNOS, inducible nitric oxide synthase; LPS, lipopolysaccharide; NQO1, quinone oxidoreductase 1; Nrf2, nuclear factor erythroid 2-related factor 2; p-ERK1/2, phosphorylated extracellular signal-regulated kinase 1/2; p-JNK, phosphorylated c-Jun-N-terminal kinase; SEM, standard error of the mean; WB, Western blotting.

    Journal: Journal of Thoracic Disease

    Article Title: Protective effects of estradiol on neuroinflammation in chronic obstructive pulmonary disease related depression

    doi: 10.21037/jtd-2025-247

    Figure Lengend Snippet: E2 promotes BV2 cell MAPKs activation and M1 polarization . (A) WB images of anti-oxidative stress protein level in BV2 cells stimulated with LPS and/or E2. (B-D) qualitative analysis of Nrf2, HO-1 and NQO1. (E) WB images of BV2 cells polarization stimulated with LPS and/or E2. (F,G) Qualitative analysis of CD163 and iNOS. (H) WB images of MAPK signaling pathway protein level in BV2 cells stimulated with LPS and/or E2. (I-K) Qualitative analysis of p-JNK, p-ERK1/2, p-p38. Data are presented as mean ± SEM, n=3. All statistical tests were conducted using two-way ANOVA. *, P<0.05, **, P<0.01, ***, P<0.001. ANOVA, analysis of variance; CTL, control; E2, estradiol; HO1, heme-oxygenase-1; iNOS, inducible nitric oxide synthase; LPS, lipopolysaccharide; NQO1, quinone oxidoreductase 1; Nrf2, nuclear factor erythroid 2-related factor 2; p-ERK1/2, phosphorylated extracellular signal-regulated kinase 1/2; p-JNK, phosphorylated c-Jun-N-terminal kinase; SEM, standard error of the mean; WB, Western blotting.

    Article Snippet: The membranes were blocked with 5% non-fat milk in TBST (Tris-buffered saline, 0.1% Tween 20) and then incubated overnight at 4 °C with primary antibodies: β-actin (1:20,000, Proteintech, #66009-1-Ig), nuclear factor erythroid 2-related factor-2 (Nrf2) (1:1,000, Proteintech, #80593-1), quinone oxidoreductase 1 (NQO1) (1:1,000, ABclonal, #A19586), heme-oxygenase-1 (HO1) (1:1,000, ABclonal, #A19062), phosphorylated nuclear factor kappa B (p-NFκB) (1:1,000, CST, #3033S), NFκB(1:1000, CST, #8242S), extracellular signal-regulated kinase 1/2 (ERK1/2) (1:1,000, Cell Signaling Technology, #4695), Phospho-ERK1/2 (1:2,000, Cell Signaling Technology, #4370), c-Jun-N-terminal kinase (JNK) (1:1,000, Cell Signaling Technology, #9252), Phospho-JNK (1:1,000, Cell Signaling Technology, #4668), Phospho-p38 (1:1,000, Cell Signaling Technology, #4511), p38 (1:1,000, Cell Signaling Technology, #9212), tumor necrosis factor α (TNF-α) (1:1,000, ABclonal, #A0277), inducible nitric oxide synthase (iNOS) (1:1,000, ImmunoWay, #YT3169), CD163 (1:1,000, ABclonal, #A8383), and CD86 (1:1,000, ABclonal, #A1199).

    Techniques: Activation Assay, Control, Western Blot