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rabbit polyclonal antibody against sod2  (Novus Biologicals)


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    Structured Review

    Novus Biologicals rabbit polyclonal antibody against sod2
    The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) <t>SOD2</t> and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice
    Rabbit Polyclonal Antibody Against Sod2, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 53 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibody against sod2/product/Novus Biologicals
    Average 93 stars, based on 53 article reviews
    rabbit polyclonal antibody against sod2 - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "1,25‐Dihydroxyvitamin D exerts an antiaging role by activation of Nrf2‐antioxidant signaling and inactivation of p16/p53‐senescence signaling"

    Article Title: 1,25‐Dihydroxyvitamin D exerts an antiaging role by activation of Nrf2‐antioxidant signaling and inactivation of p16/p53‐senescence signaling

    Journal: Aging Cell

    doi: 10.1111/acel.12951

    The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) SOD2 and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice
    Figure Legend Snippet: The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) SOD2 and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice

    Techniques Used: Expressing, Isolation, Staining, Western Blot, Control



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    Novus Biologicals rabbit polyclonal antibody against sod2
    The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) <t>SOD2</t> and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice
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    The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) <t>SOD2</t> and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice
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    The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) <t>SOD2</t> and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice
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    The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) <t>SOD2</t> and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice
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    Differentially expressed mitochondria associated genes in RC77T/E versus RC77N/E.
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    Image Search Results


    The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) SOD2 and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice

    Journal: Aging Cell

    Article Title: 1,25‐Dihydroxyvitamin D exerts an antiaging role by activation of Nrf2‐antioxidant signaling and inactivation of p16/p53‐senescence signaling

    doi: 10.1111/acel.12951

    Figure Lengend Snippet: The effects of a high calcium/phosphate diet, of 1,25(OH) 2 D 3, and of antioxidant supplementation on oxidative stress, DNA damage, and protein expression of oncogenes and tumor suppressive genes in 1α(OH)ase −/− mice. Mice from each group were treated as described in Figure . ROS levels in freshly isolated cells of (a) skin, (b) liver, and (c) kidney from 10‐week‐old wild‐type (WT) and 1α(OH)ase −/− (KO) mice. Representative micrographs of skin sections stained immunohistochemically for (d) SOD2 and (f) γ‐H2AX. Scale bars represent 50 μm in d and f. (e) The percentage of SOD2‐positive cells of skin and (g) the percentage of γ‐H2AX‐positive cells of skin; (h) representative Western blots of skin extracts to determine Prdx I protein levels. β‐actin was used as loading control. (i) Skin Prdx I and Bmi1, p16, p53 and p21 protein levels in (j) skin and (k) liver relative to β‐actin protein levels were assessed by densitometric analysis and expressed as a percentage of the levels of vehicle‐treated wild‐type mice fed the normal diet (ND).Each value is the mean ± SEM of determinations in five mice of each group. * p < 0.05; ** p < 0.01; *** p < 0.001 compared with WT mice. # p < 0.05; ## p < 0.01 compared with ND KO mice. & p < 0.05; && p < 0.01 compared with RD KO mice

    Article Snippet: Immunohistochemical staining was carried out for Ki‐67, phosphorylation of histone H2AX on Ser139 (γ‐H2AX), and superoxide dismutase 2 (SOD2) using the avidin–biotin–peroxidase complex technique with affinity‐purified rabbit polyclonal antibody against Ki‐67 (ab16667; Abcam), rabbit polyclonal antibody against γ‐H2AX (#9718; Cell Signaling Technology), and rabbit polyclonal antibody against SOD2 (NB100‐1992; Novus Biological).

    Techniques: Expressing, Isolation, Staining, Western Blot, Control

    Differentially expressed mitochondria associated genes in RC77T/E versus RC77N/E.

    Journal: BioMed Research International

    Article Title: Mitochondria Biogenesis and Bioenergetics Gene Profiles in Isogenic Prostate Cells with Different Malignant Phenotypes

    doi: 10.1155/2016/1785201

    Figure Lengend Snippet: Differentially expressed mitochondria associated genes in RC77T/E versus RC77N/E.

    Article Snippet: Goat polyclonal antibodies against human UCP2 (sc-6526), rabbit polyclonal antibodies against SOD2 (sc-30080), and rabbit polyclonal antibodies against GAPDH (sc-25778) were from Santa Cruz Biotechnology Inc. All prostatectomy tissue samples were collected from patients after informed consent following Institutional Review Board-approved protocols at the Eastern Virginia Medical School.

    Techniques: Membrane, Translocation Assay, Phospho-proteomics

    Validation of differential expression of mitochondrial uncoupling protein-2 and SOD2 in RC77N/E and RC77T/E in cell lysates. Normalized total protein lysates from the two cell lines were subjected to Western blot analysis to detect UCP2 (a) and SOD2 (b). All the samples were normalized with respect to GAPDH, which was included as a loading control. The corresponding ImageJ and normalized densitometry comparisons are shown in (c) and (d), respectively.

    Journal: BioMed Research International

    Article Title: Mitochondria Biogenesis and Bioenergetics Gene Profiles in Isogenic Prostate Cells with Different Malignant Phenotypes

    doi: 10.1155/2016/1785201

    Figure Lengend Snippet: Validation of differential expression of mitochondrial uncoupling protein-2 and SOD2 in RC77N/E and RC77T/E in cell lysates. Normalized total protein lysates from the two cell lines were subjected to Western blot analysis to detect UCP2 (a) and SOD2 (b). All the samples were normalized with respect to GAPDH, which was included as a loading control. The corresponding ImageJ and normalized densitometry comparisons are shown in (c) and (d), respectively.

    Article Snippet: Goat polyclonal antibodies against human UCP2 (sc-6526), rabbit polyclonal antibodies against SOD2 (sc-30080), and rabbit polyclonal antibodies against GAPDH (sc-25778) were from Santa Cruz Biotechnology Inc. All prostatectomy tissue samples were collected from patients after informed consent following Institutional Review Board-approved protocols at the Eastern Virginia Medical School.

    Techniques: Biomarker Discovery, Quantitative Proteomics, Western Blot, Control

    Top five canonical pathways associated with differentially expressed genes between RC77T/E and RC77N/E.

    Journal: BioMed Research International

    Article Title: Mitochondria Biogenesis and Bioenergetics Gene Profiles in Isogenic Prostate Cells with Different Malignant Phenotypes

    doi: 10.1155/2016/1785201

    Figure Lengend Snippet: Top five canonical pathways associated with differentially expressed genes between RC77T/E and RC77N/E.

    Article Snippet: Goat polyclonal antibodies against human UCP2 (sc-6526), rabbit polyclonal antibodies against SOD2 (sc-30080), and rabbit polyclonal antibodies against GAPDH (sc-25778) were from Santa Cruz Biotechnology Inc. All prostatectomy tissue samples were collected from patients after informed consent following Institutional Review Board-approved protocols at the Eastern Virginia Medical School.

    Techniques: Phospho-proteomics

    Top upstream regulators and target molecules in the regulatory network.

    Journal: BioMed Research International

    Article Title: Mitochondria Biogenesis and Bioenergetics Gene Profiles in Isogenic Prostate Cells with Different Malignant Phenotypes

    doi: 10.1155/2016/1785201

    Figure Lengend Snippet: Top upstream regulators and target molecules in the regulatory network.

    Article Snippet: Goat polyclonal antibodies against human UCP2 (sc-6526), rabbit polyclonal antibodies against SOD2 (sc-30080), and rabbit polyclonal antibodies against GAPDH (sc-25778) were from Santa Cruz Biotechnology Inc. All prostatectomy tissue samples were collected from patients after informed consent following Institutional Review Board-approved protocols at the Eastern Virginia Medical School.

    Techniques: