heme oxygenase 1 hox sc 10789 antibodies Search Results


heme oxygenase 1 ho 1 antibody  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology heme oxygenase 1 ho 1 antibody
Heme Oxygenase 1 Ho 1 Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti heme oxygenase 1 antibody  (Santa Cruz Biotechnology)
97
Santa Cruz Biotechnology anti heme oxygenase 1 antibody
Anti Heme Oxygenase 1 Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti heme oxygenase 1 antibody - by Bioz Stars, 2026-02
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heme oxygenase‑1 (ho‑1  (Santa Cruz Biotechnology)
90
Santa Cruz Biotechnology heme oxygenase‑1 (ho‑1
Heme Oxygenase‑1 (Ho‑1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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heme oxygenase 1 ho 1 rabbit polyclonal igg  (Santa Cruz Biotechnology)
97
Santa Cruz Biotechnology heme oxygenase 1 ho 1 rabbit polyclonal igg
Fig. 9 Effect of flavonoids on UVA-affected <t>HO-1</t> level and expression in NHDF. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05
Heme Oxygenase 1 Ho 1 Rabbit Polyclonal Igg, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 97 stars, based on 1 article reviews
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hmox1 ho 1  (Proteintech)
96
Proteintech hmox1 ho 1
Fig. 9 Effect of flavonoids on UVA-affected <t>HO-1</t> level and expression in NHDF. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05
Hmox1 Ho 1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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heme oxygenase 1 (hox) antibody  (Santa Cruz Biotechnology)
90
Santa Cruz Biotechnology heme oxygenase 1 (hox) antibody
Fig. 9 Effect of flavonoids on UVA-affected <t>HO-1</t> level and expression in NHDF. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05
Heme Oxygenase 1 (Hox) Antibody, supplied by Santa Cruz Biotechnology, 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/result/heme oxygenase 1 (hox) antibody/product/Santa Cruz Biotechnology
Average 90 stars, based on 1 article reviews
heme oxygenase 1 (hox) antibody - by Bioz Stars, 2026-02
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heme oxygenase 1  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology heme oxygenase 1
Fig. 9 Effect of flavonoids on UVA-affected <t>HO-1</t> level and expression in NHDF. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05
Heme Oxygenase 1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/heme oxygenase 1/product/Santa Cruz Biotechnology
Average 93 stars, based on 1 article reviews
heme oxygenase 1 - by Bioz Stars, 2026-02
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heme oxygenase-1 h-105 sc-10789 antibody  (Santa Cruz Biotechnology)
90
Santa Cruz Biotechnology heme oxygenase-1 h-105 sc-10789 antibody
Fig. 9 Effect of flavonoids on UVA-affected <t>HO-1</t> level and expression in NHDF. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05
Heme Oxygenase 1 H 105 Sc 10789 Antibody, supplied by Santa Cruz Biotechnology, 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/result/heme oxygenase-1 h-105 sc-10789 antibody/product/Santa Cruz Biotechnology
Average 90 stars, based on 1 article reviews
heme oxygenase-1 h-105 sc-10789 antibody - by Bioz Stars, 2026-02
90/100 stars
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anti heme oxygenase 1  (Santa Cruz Biotechnology)
98
Santa Cruz Biotechnology anti heme oxygenase 1
Fig. 9 Effect of flavonoids on UVA-affected <t>HO-1</t> level and expression in NHDF. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05
Anti Heme Oxygenase 1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti heme oxygenase 1/product/Santa Cruz Biotechnology
Average 98 stars, based on 1 article reviews
anti heme oxygenase 1 - by Bioz Stars, 2026-02
98/100 stars
  Buy from Supplier

Image Search Results


Fig. 9 Effect of flavonoids on UVA-affected HO-1 level and expression in NHDF. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology

Article Title: Effect of the flavonoids quercetin and taxifolin on UVA-induced damage to human primary skin keratinocytes and fibroblasts.

doi: 10.1007/s43630-021-00140-9

Figure Lengend Snippet: Fig. 9 Effect of flavonoids on UVA-affected HO-1 level and expression in NHDF. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05

Article Snippet: Western blotting luminol reagent (ImmunoCruzTM) for chemiluminescent horseradish peroxidase (HRP) detection, Nrf2 rabbit polyclonal IgG (C-20, sc-722), heme oxygenase 1 (HO-1) rabbit polyclonal IgG (H-105, sc-10789), NQO1 goat polyclonal IgG (R-20, sc-16463), catalase (CAT) rabbit polyclonal IgG (sc-50508), caspase-3 rabbit polyclonal IgG (for detection of pro-caspase-3 and caspase-3), actin goat polyclonal IgG (I-19, sc-1616), goat anti-rabbit and rabbit antigoat HRP-conjugated secondary antibody were purchased from Santa Cruz Biotechnology Inc. (USA).

Techniques: Expressing, Western Blot, Irradiation, Incubation, Control

Fig. 10 Effect of flavonoids on UVA-affected HO-1 level and expression in NHEK. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). NHEK pre-treated with TA and QE (1 h) were non-irradiated (− UVA) or exposed to 10 J/ cm2 (+ UVA). After incubation (6 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analysis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology

Article Title: Effect of the flavonoids quercetin and taxifolin on UVA-induced damage to human primary skin keratinocytes and fibroblasts.

doi: 10.1007/s43630-021-00140-9

Figure Lengend Snippet: Fig. 10 Effect of flavonoids on UVA-affected HO-1 level and expression in NHEK. HO-1 protein level was analysed by Western blot (A) and HO-1 mRNA level by qPCR (B). NHEK pre-treated with TA and QE (1 h) were non-irradiated (− UVA) or exposed to 10 J/ cm2 (+ UVA). After incubation (6 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analysis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05

Article Snippet: Western blotting luminol reagent (ImmunoCruzTM) for chemiluminescent horseradish peroxidase (HRP) detection, Nrf2 rabbit polyclonal IgG (C-20, sc-722), heme oxygenase 1 (HO-1) rabbit polyclonal IgG (H-105, sc-10789), NQO1 goat polyclonal IgG (R-20, sc-16463), catalase (CAT) rabbit polyclonal IgG (sc-50508), caspase-3 rabbit polyclonal IgG (for detection of pro-caspase-3 and caspase-3), actin goat polyclonal IgG (I-19, sc-1616), goat anti-rabbit and rabbit antigoat HRP-conjugated secondary antibody were purchased from Santa Cruz Biotechnology Inc. (USA).

Techniques: Expressing, Western Blot, Irradiation, Incubation, Control

Fig. 11 Effect of flavonoids on UVA-affected NQO1 level and expression in NHDF. NQO1 protein level was analysed by Western blot (A) and NQO1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology

Article Title: Effect of the flavonoids quercetin and taxifolin on UVA-induced damage to human primary skin keratinocytes and fibroblasts.

doi: 10.1007/s43630-021-00140-9

Figure Lengend Snippet: Fig. 11 Effect of flavonoids on UVA-affected NQO1 level and expression in NHDF. NQO1 protein level was analysed by Western blot (A) and NQO1 mRNA level by qPCR (B). Fibroblasts pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 7.5 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05. #Significantly different from control cells at p = 0.05

Article Snippet: Western blotting luminol reagent (ImmunoCruzTM) for chemiluminescent horseradish peroxidase (HRP) detection, Nrf2 rabbit polyclonal IgG (C-20, sc-722), heme oxygenase 1 (HO-1) rabbit polyclonal IgG (H-105, sc-10789), NQO1 goat polyclonal IgG (R-20, sc-16463), catalase (CAT) rabbit polyclonal IgG (sc-50508), caspase-3 rabbit polyclonal IgG (for detection of pro-caspase-3 and caspase-3), actin goat polyclonal IgG (I-19, sc-1616), goat anti-rabbit and rabbit antigoat HRP-conjugated secondary antibody were purchased from Santa Cruz Biotechnology Inc. (USA).

Techniques: Expressing, Western Blot, Irradiation, Incubation, Control

Fig. 12 Effect of flavonoids on UVA-affected NQO1 level and expression NHEK. NQO1 protein level was analysed by Western blot (A) and NQO1 mRNA level by qPCR (B). Keratinocytes pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 10 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology

Article Title: Effect of the flavonoids quercetin and taxifolin on UVA-induced damage to human primary skin keratinocytes and fibroblasts.

doi: 10.1007/s43630-021-00140-9

Figure Lengend Snippet: Fig. 12 Effect of flavonoids on UVA-affected NQO1 level and expression NHEK. NQO1 protein level was analysed by Western blot (A) and NQO1 mRNA level by qPCR (B). Keratinocytes pre-treated with TA and QE (1 h) were non- irradiated (− UVA) or exposed to 10 J/cm2 (+ UVA). After incubation (24 h), HO-1 level was evaluated as described in Materials and Methods. Data are normalized to the reference protein actin and gene GAPDH. Results are mean ± SD of 3 experiments employing cells from 3 donors. Representative examples of Western blot analy- sis are shown. *Significantly different from irradiated control cells at p = 0.05

Article Snippet: Western blotting luminol reagent (ImmunoCruzTM) for chemiluminescent horseradish peroxidase (HRP) detection, Nrf2 rabbit polyclonal IgG (C-20, sc-722), heme oxygenase 1 (HO-1) rabbit polyclonal IgG (H-105, sc-10789), NQO1 goat polyclonal IgG (R-20, sc-16463), catalase (CAT) rabbit polyclonal IgG (sc-50508), caspase-3 rabbit polyclonal IgG (for detection of pro-caspase-3 and caspase-3), actin goat polyclonal IgG (I-19, sc-1616), goat anti-rabbit and rabbit antigoat HRP-conjugated secondary antibody were purchased from Santa Cruz Biotechnology Inc. (USA).

Techniques: Expressing, Western Blot, Irradiation, Incubation, Control