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ho 1  (OriGene)


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    Structured Review

    OriGene ho 1
    SWE 160.1 treatment increased the antioxidant response. ( a ) Western blotting analysis of antioxidant factors <t>(HO-1,</t> SOD-2 and Nrf2) after 48 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Protein levels were normalized to γ-tubulin. ( b ) qRT-PCR analysis of Nrf2, Keap1 and HO-1 mRNA levels after 24 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Gene expression levels represent the relative mRNA expression compared to the untreated cells, normalized to GAPDH mRNA. ( c ) Western blotting of subcellular fractions of control and 48 h SWE 160.1 -treated cells incubated with pNrf2 (Ser40) antibody. Lamin A and GADPH antibodies marked as nuclei (N) and cytoplasmic (C) fractions, respectively. The images are representative of three different experiments. * p < 0.05, ** p < 0.01 vs. untreated control cells.
    Ho 1, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ho+1/Heme+Oxygenase+1+(HMOX1)+Human+qPCR+Primer+Pair/pmc13209369-269-20-24
    Average 94 stars, based on 4 article reviews
    ho 1 - by Bioz Stars, 2026-09
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    Images

    1) Product Images from "Subcritical Water Extract from Grape Pomace Protects Human Bronchial Epithelium Cells by Mitigating Oxidative Stress Through Nrf2 Pathway"

    Article Title: Subcritical Water Extract from Grape Pomace Protects Human Bronchial Epithelium Cells by Mitigating Oxidative Stress Through Nrf2 Pathway

    Journal: Molecules

    doi: 10.3390/molecules31101736

    SWE 160.1 treatment increased the antioxidant response. ( a ) Western blotting analysis of antioxidant factors (HO-1, SOD-2 and Nrf2) after 48 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Protein levels were normalized to γ-tubulin. ( b ) qRT-PCR analysis of Nrf2, Keap1 and HO-1 mRNA levels after 24 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Gene expression levels represent the relative mRNA expression compared to the untreated cells, normalized to GAPDH mRNA. ( c ) Western blotting of subcellular fractions of control and 48 h SWE 160.1 -treated cells incubated with pNrf2 (Ser40) antibody. Lamin A and GADPH antibodies marked as nuclei (N) and cytoplasmic (C) fractions, respectively. The images are representative of three different experiments. * p < 0.05, ** p < 0.01 vs. untreated control cells.
    Figure Legend Snippet: SWE 160.1 treatment increased the antioxidant response. ( a ) Western blotting analysis of antioxidant factors (HO-1, SOD-2 and Nrf2) after 48 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Protein levels were normalized to γ-tubulin. ( b ) qRT-PCR analysis of Nrf2, Keap1 and HO-1 mRNA levels after 24 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Gene expression levels represent the relative mRNA expression compared to the untreated cells, normalized to GAPDH mRNA. ( c ) Western blotting of subcellular fractions of control and 48 h SWE 160.1 -treated cells incubated with pNrf2 (Ser40) antibody. Lamin A and GADPH antibodies marked as nuclei (N) and cytoplasmic (C) fractions, respectively. The images are representative of three different experiments. * p < 0.05, ** p < 0.01 vs. untreated control cells.

    Techniques Used: Western Blot, Quantitative RT-PCR, Gene Expression, Expressing, Control, Incubation

    SWE 160.1 treatment overwhelmed LPS-induced HO-1-reduction. Western blotting analysis of HO-1 enzyme after 48 h of treatment with 2 µg/mL LPS alone or in combination with 100 µg GAE/mL SWE 160.1 . Protein levels were normalized to γ-tubulin. Densitometric analysis, performed using Quantity One software, (version 4.6.6), is shown in the histogram. The result is representative of two independent experiments, with values expressed as mean ± SD. ** p < 0.01 vs. untreated control cells.
    Figure Legend Snippet: SWE 160.1 treatment overwhelmed LPS-induced HO-1-reduction. Western blotting analysis of HO-1 enzyme after 48 h of treatment with 2 µg/mL LPS alone or in combination with 100 µg GAE/mL SWE 160.1 . Protein levels were normalized to γ-tubulin. Densitometric analysis, performed using Quantity One software, (version 4.6.6), is shown in the histogram. The result is representative of two independent experiments, with values expressed as mean ± SD. ** p < 0.01 vs. untreated control cells.

    Techniques Used: Western Blot, Software, Control

    Related Articles

    Incubation:

    Article Title: HO-1 Limits the Efficacy of Vemurafenib/PLX4032 in BRAF V600E Mutated Melanoma Cells Adapted to Physiological Normoxia or Hypoxia
    Article Snippet: Protein cell lysates were denaturated in Laemmli buffer, subjected to SDS-polyacrylamide gel electrophoresis (200 Volt for 50 min) using 4–20% Mini-Protean TGX TM Gels precast (Bio-Rad). .. After blotting, PVDF membranes (GE Healthcare, Amersham Place, UK) were blocked in non-fat dry milk (5% w / v in 1X tTBS) and then incubated with antibodies against ERK, p-ERK (1:1000, rabbit polyclonal antibody, Cell Signaling Technology, Leiden, The Netherlands), HO-1 (1:2000, rabbit polyclonal antibody, ORIGENE, Herford, Germany), Bach1 (1:4000, rabbit polyclonal antibody, Bethyl Lab, Montgomery, TX, USA), and HIF-1α (1:1000, rabbit polyclonal antibody, Abcam, Cambridge, UK). .. Bands were detected by enhanced chemiluminescence (GE Healthcare) after incubation with specific secondary antibodies (1:10,000, anti-rabbit and anti-mouse, GE Healthcare).

    Expressing:

    Article Title: Differentiation impairs Bach1 dependent HO-1 activation and increases sensitivity to oxidative stress in SH-SY5Y neuroblastoma cells
    Article Snippet: Developed films were analysed using a specific software (GelDoc; Bio-Rad). .. To study HO-1 expression, SH-SY5Y cells were grown as wild type or differentiated in 8-well chamber slides and then exposed to 500 μM H 2 O 2 or 50 μM tBHQ for 24 h. By means of a standard technique of immunofluorescence (fixing in cold methanol), HO-1 expression was detected by using anti HO-1 (10 μg/ml rabbit anti HO-1, Origene) and ALEXA 633 (anti rabbit 1:400, Life-Technologies). .. Images were collected by using a three-channel TCS SP2 laser scanning confocal microscope (Leica Mycrosystems).

    Immunofluorescence:

    Article Title: Differentiation impairs Bach1 dependent HO-1 activation and increases sensitivity to oxidative stress in SH-SY5Y neuroblastoma cells
    Article Snippet: Developed films were analysed using a specific software (GelDoc; Bio-Rad). .. To study HO-1 expression, SH-SY5Y cells were grown as wild type or differentiated in 8-well chamber slides and then exposed to 500 μM H 2 O 2 or 50 μM tBHQ for 24 h. By means of a standard technique of immunofluorescence (fixing in cold methanol), HO-1 expression was detected by using anti HO-1 (10 μg/ml rabbit anti HO-1, Origene) and ALEXA 633 (anti rabbit 1:400, Life-Technologies). .. Images were collected by using a three-channel TCS SP2 laser scanning confocal microscope (Leica Mycrosystems).

    Transfection:

    Article Title: Mitochondrial quality-control dysregulation in conditional HO-1 –/– mice
    Article Snippet: HL-1 cardiomyocytes (1 × 10 4 per treatment) were cultured in flasks coated in fibronectin (12.5 mg/l) gelatin (0.02%) containing Claycomb medium (Sigma-Aldrich) supplemented with 10% FBS (PAN Biotech GmbH), 2 mM L-glutamine (PAN Biotech GmbH), 0.1 mM norepinephrine (Sigma-Aldrich), ascorbic acid 0.3 mM (Sigma-Aldrich), 100 U/ml penicillin (Sigma-Aldrich), and 100 μg/ml streptomycin (Sigma-Aldrich) in a humid atmosphere of 5% CO 2 /95% air at 37°C ( 5 ). .. Cells were transfected in 6-well plates at 70%–80% confluence with pGFPCRS vector containing HO-1 oligonucleotide sequence for optimal suppression of HO-1 (Origene, TR30018), HO-1 TrueORF (Origene, MR203944), or NRF-1 TrueORF (Origene, MG208550) using FuGENE-HD (Promega, E2311). ..

    Article Title: Nuclear respiratory factor-1 negatively regulates TGF-β1 and attenuates pulmonary fibrosis
    Article Snippet: .. Cells were transfected in 6-well plates at 70%–80% confluence with pGFPCRS vector containing HO-1 oligonucleotide sequence for optimal suppression of HO-1 (Origene, TR30018), NRF-1 (Origene, TF517273) or CCN5 (Origene, TF511452). .. For overexpression, HO-1 TrueORF (Origene, MR203944), NRF-1 TrueORF (Origene, MG208550), or CCN5 (Origene, RC204636) was used with FuGENE-HD (Promega, E2311).

    Article Title: Adipocyte-activated oxidative and ER stress pathways promote tumor survival in bone via upregulation of Heme Oxygenase 1 and Survivin
    Article Snippet: ARCaP(M) cells, an androgen-repressed metastatic prostate cancer M (‘Mesenchymal’ clone) cells, were purchased from Novicure Biotechnology (Birmingham, AL, USA). .. Both lines were stably transfected with empty vector (E) and HO-1 (H) via myc-DDK vector plasmids (OriGene, Rockville, MD), which contain the neomycin-resistant gene. ..

    Sequencing:

    Article Title: Mitochondrial quality-control dysregulation in conditional HO-1 –/– mice
    Article Snippet: HL-1 cardiomyocytes (1 × 10 4 per treatment) were cultured in flasks coated in fibronectin (12.5 mg/l) gelatin (0.02%) containing Claycomb medium (Sigma-Aldrich) supplemented with 10% FBS (PAN Biotech GmbH), 2 mM L-glutamine (PAN Biotech GmbH), 0.1 mM norepinephrine (Sigma-Aldrich), ascorbic acid 0.3 mM (Sigma-Aldrich), 100 U/ml penicillin (Sigma-Aldrich), and 100 μg/ml streptomycin (Sigma-Aldrich) in a humid atmosphere of 5% CO 2 /95% air at 37°C ( 5 ). .. Cells were transfected in 6-well plates at 70%–80% confluence with pGFPCRS vector containing HO-1 oligonucleotide sequence for optimal suppression of HO-1 (Origene, TR30018), HO-1 TrueORF (Origene, MR203944), or NRF-1 TrueORF (Origene, MG208550) using FuGENE-HD (Promega, E2311). ..

    Article Title: Nuclear respiratory factor-1 negatively regulates TGF-β1 and attenuates pulmonary fibrosis
    Article Snippet: .. Cells were transfected in 6-well plates at 70%–80% confluence with pGFPCRS vector containing HO-1 oligonucleotide sequence for optimal suppression of HO-1 (Origene, TR30018), NRF-1 (Origene, TF517273) or CCN5 (Origene, TF511452). .. For overexpression, HO-1 TrueORF (Origene, MR203944), NRF-1 TrueORF (Origene, MG208550), or CCN5 (Origene, RC204636) was used with FuGENE-HD (Promega, E2311).

    other:

    Article Title: Lipoperoxide Nanoemulsion as Adjuvant in Cisplatin Cancer Therapy: In Vitro Study on Human Colon Adenocarcinoma DLD-1 Cells
    Article Snippet: HO-1 (TA327035) , 32 , Origene, Rockville, MD, USA.

    Stable Transfection:

    Article Title: Adipocyte-activated oxidative and ER stress pathways promote tumor survival in bone via upregulation of Heme Oxygenase 1 and Survivin
    Article Snippet: ARCaP(M) cells, an androgen-repressed metastatic prostate cancer M (‘Mesenchymal’ clone) cells, were purchased from Novicure Biotechnology (Birmingham, AL, USA). .. Both lines were stably transfected with empty vector (E) and HO-1 (H) via myc-DDK vector plasmids (OriGene, Rockville, MD), which contain the neomycin-resistant gene. ..

    Plasmid Preparation:

    Article Title: Adipocyte-activated oxidative and ER stress pathways promote tumor survival in bone via upregulation of Heme Oxygenase 1 and Survivin
    Article Snippet: ARCaP(M) cells, an androgen-repressed metastatic prostate cancer M (‘Mesenchymal’ clone) cells, were purchased from Novicure Biotechnology (Birmingham, AL, USA). .. Both lines were stably transfected with empty vector (E) and HO-1 (H) via myc-DDK vector plasmids (OriGene, Rockville, MD), which contain the neomycin-resistant gene. ..

    Nucleic Acid Electrophoresis:

    Article Title: HO-1 downregulation favors BRAF V600 melanoma cell death induced by Vemurafenib/PLX4032 and increases NK recognition.
    Article Snippet: Heme oxygenase 1 (HO-1) plays a pivotal role in preventing cell damage.. Indeed, through the antioxidant, anti-apoptotic and anti-inflammatory properties of its metabolic products, it favors cell adaptation against different stressors.. However, HO-1 induction has also been related to the gain of resistance to therapy in different types of cancers and its involvement in cancer immune-escape has been hypothesized.



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    SWE 160.1 treatment increased the antioxidant response. ( a ) Western blotting analysis of antioxidant factors <t>(HO-1,</t> SOD-2 and Nrf2) after 48 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Protein levels were normalized to γ-tubulin. ( b ) qRT-PCR analysis of Nrf2, Keap1 and HO-1 mRNA levels after 24 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Gene expression levels represent the relative mRNA expression compared to the untreated cells, normalized to GAPDH mRNA. ( c ) Western blotting of subcellular fractions of control and 48 h SWE 160.1 -treated cells incubated with pNrf2 (Ser40) antibody. Lamin A and GADPH antibodies marked as nuclei (N) and cytoplasmic (C) fractions, respectively. The images are representative of three different experiments. * p < 0.05, ** p < 0.01 vs. untreated control cells.
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    Image Search Results


    BBR684 attenuates Erastin-induced ferroptosis in HK-2 cells by suppressing lipid peroxidation and activating the antioxidant response. (A) Flow cytometric analysis of lipid peroxidation using the C11-BODIPY probe in HK-2 cells treated as indicated for 12 hours. Data are presented as mean fluorescence intensity (MFI). (B) Intracellular Fe²⁺ levels measured by a ferrous iron colorimetric assay. (C, D) Levels of malondialdehyde (MDA, C) and reduced glutathione (GSH, D) in cell lysates. (E, F) Representative immunofluorescence images (E) and quantification (F) of 4-hydroxynonenal (4-HNE) adducts (red) in HK-2 cells. Nuclei were counterstained with DAPI (blue). Scale bar, 50 µm. (G) Western blot analysis of key ferroptosis-related proteins: glutathione peroxidase 4 (GPX4), heme oxygenase-1 (HO-1), and nuclear factor erythroid 2–related factor 2 (NRF2). β-actin served as the loading control. Data are from 3 independent biological replicates (n = 3) and presented as mean ± SEM. Significance was determined by one-way ANOVA followed by Tukey's HSD post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001; n.s., not significant.

    Journal: Current Therapeutic Research, Clinical and Experimental

    Article Title: The Berberine Derivative BBR684 Inhibits VDAC Oligomerization to Suppress Ferroptosis in Acute Kidney Injury

    doi: 10.1016/j.curtheres.2026.100825

    Figure Lengend Snippet: BBR684 attenuates Erastin-induced ferroptosis in HK-2 cells by suppressing lipid peroxidation and activating the antioxidant response. (A) Flow cytometric analysis of lipid peroxidation using the C11-BODIPY probe in HK-2 cells treated as indicated for 12 hours. Data are presented as mean fluorescence intensity (MFI). (B) Intracellular Fe²⁺ levels measured by a ferrous iron colorimetric assay. (C, D) Levels of malondialdehyde (MDA, C) and reduced glutathione (GSH, D) in cell lysates. (E, F) Representative immunofluorescence images (E) and quantification (F) of 4-hydroxynonenal (4-HNE) adducts (red) in HK-2 cells. Nuclei were counterstained with DAPI (blue). Scale bar, 50 µm. (G) Western blot analysis of key ferroptosis-related proteins: glutathione peroxidase 4 (GPX4), heme oxygenase-1 (HO-1), and nuclear factor erythroid 2–related factor 2 (NRF2). β-actin served as the loading control. Data are from 3 independent biological replicates (n = 3) and presented as mean ± SEM. Significance was determined by one-way ANOVA followed by Tukey's HSD post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001; n.s., not significant.

    Article Snippet: Antibodies against GPX4 (Catalog #3F5G5), HO-1 (Catalog #10701-1-AP), NRF2 (Catalog #16396-1-AP), VDAC (Catalog #10866-1-AP), Cleaved Caspase-3 (Catalog #68773-1-Ig), and CD45 (Catalog #98035-1-RR) were purchased from Proteintech.

    Techniques: Fluorescence, Colorimetric Assay, Immunofluorescence, Western Blot, Control

    BBR684 attenuates Erastin-induced ferroptosis in HK-2 cells by suppressing lipid peroxidation and activating the antioxidant response. (A) Flow cytometric analysis of lipid peroxidation using the C11-BODIPY probe in HK-2 cells treated as indicated for 12 hours. Data are presented as mean fluorescence intensity (MFI). (B) Intracellular Fe²⁺ levels measured by a ferrous iron colorimetric assay. (C, D) Levels of malondialdehyde (MDA, C) and reduced glutathione (GSH, D) in cell lysates. (E, F) Representative immunofluorescence images (E) and quantification (F) of 4-hydroxynonenal (4-HNE) adducts (red) in HK-2 cells. Nuclei were counterstained with DAPI (blue). Scale bar, 50 µm. (G) Western blot analysis of key ferroptosis-related proteins: glutathione peroxidase 4 (GPX4), heme oxygenase-1 (HO-1), and nuclear factor erythroid 2–related factor 2 (NRF2). β-actin served as the loading control. Data are from 3 independent biological replicates (n = 3) and presented as mean ± SEM. Significance was determined by one-way ANOVA followed by Tukey's HSD post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001; n.s., not significant.

    Journal: Current Therapeutic Research, Clinical and Experimental

    Article Title: The Berberine Derivative BBR684 Inhibits VDAC Oligomerization to Suppress Ferroptosis in Acute Kidney Injury

    doi: 10.1016/j.curtheres.2026.100825

    Figure Lengend Snippet: BBR684 attenuates Erastin-induced ferroptosis in HK-2 cells by suppressing lipid peroxidation and activating the antioxidant response. (A) Flow cytometric analysis of lipid peroxidation using the C11-BODIPY probe in HK-2 cells treated as indicated for 12 hours. Data are presented as mean fluorescence intensity (MFI). (B) Intracellular Fe²⁺ levels measured by a ferrous iron colorimetric assay. (C, D) Levels of malondialdehyde (MDA, C) and reduced glutathione (GSH, D) in cell lysates. (E, F) Representative immunofluorescence images (E) and quantification (F) of 4-hydroxynonenal (4-HNE) adducts (red) in HK-2 cells. Nuclei were counterstained with DAPI (blue). Scale bar, 50 µm. (G) Western blot analysis of key ferroptosis-related proteins: glutathione peroxidase 4 (GPX4), heme oxygenase-1 (HO-1), and nuclear factor erythroid 2–related factor 2 (NRF2). β-actin served as the loading control. Data are from 3 independent biological replicates (n = 3) and presented as mean ± SEM. Significance was determined by one-way ANOVA followed by Tukey's HSD post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001; n.s., not significant.

    Article Snippet: Antibodies against GPX4 (Catalog #3F5G5), HO-1 (Catalog #10701-1-AP), NRF2 (Catalog #16396-1-AP), VDAC (Catalog #10866-1-AP), Cleaved Caspase-3 (Catalog #68773-1-Ig), and CD45 (Catalog #98035-1-RR) were purchased from Proteintech.

    Techniques: Fluorescence, Colorimetric Assay, Immunofluorescence, Western Blot, Control

    SWE 160.1 treatment increased the antioxidant response. ( a ) Western blotting analysis of antioxidant factors (HO-1, SOD-2 and Nrf2) after 48 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Protein levels were normalized to γ-tubulin. ( b ) qRT-PCR analysis of Nrf2, Keap1 and HO-1 mRNA levels after 24 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Gene expression levels represent the relative mRNA expression compared to the untreated cells, normalized to GAPDH mRNA. ( c ) Western blotting of subcellular fractions of control and 48 h SWE 160.1 -treated cells incubated with pNrf2 (Ser40) antibody. Lamin A and GADPH antibodies marked as nuclei (N) and cytoplasmic (C) fractions, respectively. The images are representative of three different experiments. * p < 0.05, ** p < 0.01 vs. untreated control cells.

    Journal: Molecules

    Article Title: Subcritical Water Extract from Grape Pomace Protects Human Bronchial Epithelium Cells by Mitigating Oxidative Stress Through Nrf2 Pathway

    doi: 10.3390/molecules31101736

    Figure Lengend Snippet: SWE 160.1 treatment increased the antioxidant response. ( a ) Western blotting analysis of antioxidant factors (HO-1, SOD-2 and Nrf2) after 48 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Protein levels were normalized to γ-tubulin. ( b ) qRT-PCR analysis of Nrf2, Keap1 and HO-1 mRNA levels after 24 h of treatment with 75 and 100 µg GAE/mL SWE 160.1 in HBE cells. Gene expression levels represent the relative mRNA expression compared to the untreated cells, normalized to GAPDH mRNA. ( c ) Western blotting of subcellular fractions of control and 48 h SWE 160.1 -treated cells incubated with pNrf2 (Ser40) antibody. Lamin A and GADPH antibodies marked as nuclei (N) and cytoplasmic (C) fractions, respectively. The images are representative of three different experiments. * p < 0.05, ** p < 0.01 vs. untreated control cells.

    Article Snippet: The primers used were GAPDH (Proligo USA, Milan, Italy), Nrf2 ( HP209154 , OriGene Technologies, Inc., Rockville, MD, USA) and HO-1 ( HP205872 , OriGene Technologies, Inc., USA).

    Techniques: Western Blot, Quantitative RT-PCR, Gene Expression, Expressing, Control, Incubation

    SWE 160.1 treatment overwhelmed LPS-induced HO-1-reduction. Western blotting analysis of HO-1 enzyme after 48 h of treatment with 2 µg/mL LPS alone or in combination with 100 µg GAE/mL SWE 160.1 . Protein levels were normalized to γ-tubulin. Densitometric analysis, performed using Quantity One software, (version 4.6.6), is shown in the histogram. The result is representative of two independent experiments, with values expressed as mean ± SD. ** p < 0.01 vs. untreated control cells.

    Journal: Molecules

    Article Title: Subcritical Water Extract from Grape Pomace Protects Human Bronchial Epithelium Cells by Mitigating Oxidative Stress Through Nrf2 Pathway

    doi: 10.3390/molecules31101736

    Figure Lengend Snippet: SWE 160.1 treatment overwhelmed LPS-induced HO-1-reduction. Western blotting analysis of HO-1 enzyme after 48 h of treatment with 2 µg/mL LPS alone or in combination with 100 µg GAE/mL SWE 160.1 . Protein levels were normalized to γ-tubulin. Densitometric analysis, performed using Quantity One software, (version 4.6.6), is shown in the histogram. The result is representative of two independent experiments, with values expressed as mean ± SD. ** p < 0.01 vs. untreated control cells.

    Article Snippet: The primers used were GAPDH (Proligo USA, Milan, Italy), Nrf2 ( HP209154 , OriGene Technologies, Inc., Rockville, MD, USA) and HO-1 ( HP205872 , OriGene Technologies, Inc., USA).

    Techniques: Western Blot, Software, Control