dylight405 anti g6pd  (Bio-Techne corporation)


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    Bio-Techne corporation dylight405 anti g6pd
    Dylight405 Anti G6pd, supplied by Bio-Techne corporation, 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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    Tokyo Chemical Industry glucose 6 phosphate dehydrogenase g6pd
    Glucose 6 Phosphate Dehydrogenase G6pd, supplied by Tokyo Chemical Industry, 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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    MyBiosource Biotechnology glucose 6 phosphate dehydrogenase g6pd
    Levels of the following enzyme activity are represented a) Acid Phosphatase (ACP) in unit/mL, b) Creatine Kinase (CK) in ng/mL, c) <t>Glucose-6-Phosphate</t> Dehydrogenase <t>(G6PD)</t> in ng/mL and d) Sorbitol Dehydrogenase (SDH) in mIU/mL. Values are given as mean ± SEM, for ten rats per group. Values are statistically significant at * p <0.05.
    Glucose 6 Phosphate Dehydrogenase G6pd, supplied by MyBiosource Biotechnology, 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 "Effects of empagliflozin on gonadal functions of hyperglycemic male wistar rats"

    Article Title: Effects of empagliflozin on gonadal functions of hyperglycemic male wistar rats

    Journal: PLOS ONE

    doi: 10.1371/journal.pone.0305636

    Levels of the following enzyme activity are represented a) Acid Phosphatase (ACP) in unit/mL, b) Creatine Kinase (CK) in ng/mL, c) Glucose-6-Phosphate Dehydrogenase (G6PD) in ng/mL and d) Sorbitol Dehydrogenase (SDH) in mIU/mL. Values are given as mean ± SEM, for ten rats per group. Values are statistically significant at * p <0.05.
    Figure Legend Snippet: Levels of the following enzyme activity are represented a) Acid Phosphatase (ACP) in unit/mL, b) Creatine Kinase (CK) in ng/mL, c) Glucose-6-Phosphate Dehydrogenase (G6PD) in ng/mL and d) Sorbitol Dehydrogenase (SDH) in mIU/mL. Values are given as mean ± SEM, for ten rats per group. Values are statistically significant at * p <0.05.

    Techniques Used: Activity Assay

    glucose 6 phosphate dehydrogenase g6pd  (Roche)


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    Roche glucose 6 phosphate dehydrogenase g6pd
    Glucose 6 Phosphate Dehydrogenase G6pd, supplied by Roche, 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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    variance ci confidence interval epl essential phospholipids g6pd glucose 6 phosphate dehydrogenase il interleukin lps lipopolysaccharide ls  (Sanofi)

     
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    Sanofi variance ci confidence interval epl essential phospholipids g6pd glucose 6 phosphate dehydrogenase il interleukin lps lipopolysaccharide ls
    Variance Ci Confidence Interval Epl Essential Phospholipids G6pd Glucose 6 Phosphate Dehydrogenase Il Interleukin Lps Lipopolysaccharide Ls, supplied by Sanofi, 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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    yeast glucose 6 phosphate dehydrogenase g6pd  (OriGene)


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    OriGene yeast glucose 6 phosphate dehydrogenase g6pd
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    dylight405 anti g6pd  (Bio-Techne corporation)


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    Bio-Techne corporation dylight405 anti g6pd
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    dylight405 anti g6pd  (Bio-Techne corporation)


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    Bio-Techne corporation dylight405 anti g6pd
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    Bio-Rad g6pd glucose 6 phosphate dehydrogenase
    G6pd Glucose 6 Phosphate Dehydrogenase, supplied by Bio-Rad, 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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    glucose 6 phosphate dehydrogenase g6pd activity  (Danaher Inc)


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    Danaher Inc glucose 6 phosphate dehydrogenase g6pd activity
    SF alters redox homeostasis (A) Reduced glutathione (GSH) levels, (B) oxidized glutathione (GSSG) levels and (C) GSH/GSSG ratio in mouse heart tissues isolated from NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF, respectively, were measured by enzymatic recycling method. (D) <t>Glucose-6-phosphate</t> dehydrogenase <t>(G6PD)</t> activity, (E) catalase activity and (F) malondialdehyde levels measured in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. (G) Quantitative RT-PCR analysis of redox regulating genes ( Nrf2 , Nqo1 , Gclm , Gsr , Gsta , G6pd , Cat , Sod1 , and Sod2 ) in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. mRNA levels were normalized to Gapdh and presented as relative expression levels compared to level in NTg-NSF mouse heart tissues. Values are mean ± SEM. with each experiment performed in triplicates (n = 6 in each group). (H) Representative immunoblots with respective proteins from the total lysates of mouse heart tissues isolated from indicated mouse heart tissues. Expression levels were normalized to loading control and presented as relative expression levels compared with the level in NTg-NSF mouse heart tissues. Gapdh levels were used as a loading control. Values are shown as means ± SEM with each experiment performed in triplicate (n = 3 in each group). Significance was evaluated by Student’s t test or one-way analysis of variance (ANOVA) with post hoc sidak multiple comparison test, respectively. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
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    1) Product Images from "Sleep fragmentation induces heart failure in a hypertrophic cardiomyopathy mouse model by altering redox metabolism"

    Article Title: Sleep fragmentation induces heart failure in a hypertrophic cardiomyopathy mouse model by altering redox metabolism

    Journal: iScience

    doi: 10.1016/j.isci.2024.109075

    SF alters redox homeostasis (A) Reduced glutathione (GSH) levels, (B) oxidized glutathione (GSSG) levels and (C) GSH/GSSG ratio in mouse heart tissues isolated from NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF, respectively, were measured by enzymatic recycling method. (D) Glucose-6-phosphate dehydrogenase (G6PD) activity, (E) catalase activity and (F) malondialdehyde levels measured in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. (G) Quantitative RT-PCR analysis of redox regulating genes ( Nrf2 , Nqo1 , Gclm , Gsr , Gsta , G6pd , Cat , Sod1 , and Sod2 ) in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. mRNA levels were normalized to Gapdh and presented as relative expression levels compared to level in NTg-NSF mouse heart tissues. Values are mean ± SEM. with each experiment performed in triplicates (n = 6 in each group). (H) Representative immunoblots with respective proteins from the total lysates of mouse heart tissues isolated from indicated mouse heart tissues. Expression levels were normalized to loading control and presented as relative expression levels compared with the level in NTg-NSF mouse heart tissues. Gapdh levels were used as a loading control. Values are shown as means ± SEM with each experiment performed in triplicate (n = 3 in each group). Significance was evaluated by Student’s t test or one-way analysis of variance (ANOVA) with post hoc sidak multiple comparison test, respectively. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001. See also <xref ref-type=Figure S2 . " title="... respectively, were measured by enzymatic recycling method. (D) Glucose-6-phosphate dehydrogenase (G6PD) activity, (E) catalase activity and (F) ..." property="contentUrl" width="100%" height="100%"/>
    Figure Legend Snippet: SF alters redox homeostasis (A) Reduced glutathione (GSH) levels, (B) oxidized glutathione (GSSG) levels and (C) GSH/GSSG ratio in mouse heart tissues isolated from NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF, respectively, were measured by enzymatic recycling method. (D) Glucose-6-phosphate dehydrogenase (G6PD) activity, (E) catalase activity and (F) malondialdehyde levels measured in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. (G) Quantitative RT-PCR analysis of redox regulating genes ( Nrf2 , Nqo1 , Gclm , Gsr , Gsta , G6pd , Cat , Sod1 , and Sod2 ) in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. mRNA levels were normalized to Gapdh and presented as relative expression levels compared to level in NTg-NSF mouse heart tissues. Values are mean ± SEM. with each experiment performed in triplicates (n = 6 in each group). (H) Representative immunoblots with respective proteins from the total lysates of mouse heart tissues isolated from indicated mouse heart tissues. Expression levels were normalized to loading control and presented as relative expression levels compared with the level in NTg-NSF mouse heart tissues. Gapdh levels were used as a loading control. Values are shown as means ± SEM with each experiment performed in triplicate (n = 3 in each group). Significance was evaluated by Student’s t test or one-way analysis of variance (ANOVA) with post hoc sidak multiple comparison test, respectively. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001. See also Figure S2 .

    Techniques Used: Isolation, Activity Assay, Quantitative RT-PCR, Expressing, Western Blot, Comparison

    anti g6pd  (Bio-Techne corporation)


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    Bio-Techne corporation anti g6pd
    Anti G6pd, supplied by Bio-Techne corporation, 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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    Bio-Techne corporation dylight405 anti g6pd
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    Levels of the following enzyme activity are represented a) Acid Phosphatase (ACP) in unit/mL, b) Creatine Kinase (CK) in ng/mL, c) <t>Glucose-6-Phosphate</t> Dehydrogenase <t>(G6PD)</t> in ng/mL and d) Sorbitol Dehydrogenase (SDH) in mIU/mL. Values are given as mean ± SEM, for ten rats per group. Values are statistically significant at * p <0.05.
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    SF alters redox homeostasis (A) Reduced glutathione (GSH) levels, (B) oxidized glutathione (GSSG) levels and (C) GSH/GSSG ratio in mouse heart tissues isolated from NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF, respectively, were measured by enzymatic recycling method. (D) <t>Glucose-6-phosphate</t> dehydrogenase <t>(G6PD)</t> activity, (E) catalase activity and (F) malondialdehyde levels measured in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. (G) Quantitative RT-PCR analysis of redox regulating genes ( Nrf2 , Nqo1 , Gclm , Gsr , Gsta , G6pd , Cat , Sod1 , and Sod2 ) in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. mRNA levels were normalized to Gapdh and presented as relative expression levels compared to level in NTg-NSF mouse heart tissues. Values are mean ± SEM. with each experiment performed in triplicates (n = 6 in each group). (H) Representative immunoblots with respective proteins from the total lysates of mouse heart tissues isolated from indicated mouse heart tissues. Expression levels were normalized to loading control and presented as relative expression levels compared with the level in NTg-NSF mouse heart tissues. Gapdh levels were used as a loading control. Values are shown as means ± SEM with each experiment performed in triplicate (n = 3 in each group). Significance was evaluated by Student’s t test or one-way analysis of variance (ANOVA) with post hoc sidak multiple comparison test, respectively. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
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    SF alters redox homeostasis (A) Reduced glutathione (GSH) levels, (B) oxidized glutathione (GSSG) levels and (C) GSH/GSSG ratio in mouse heart tissues isolated from NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF, respectively, were measured by enzymatic recycling method. (D) <t>Glucose-6-phosphate</t> dehydrogenase <t>(G6PD)</t> activity, (E) catalase activity and (F) malondialdehyde levels measured in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. (G) Quantitative RT-PCR analysis of redox regulating genes ( Nrf2 , Nqo1 , Gclm , Gsr , Gsta , G6pd , Cat , Sod1 , and Sod2 ) in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. mRNA levels were normalized to Gapdh and presented as relative expression levels compared to level in NTg-NSF mouse heart tissues. Values are mean ± SEM. with each experiment performed in triplicates (n = 6 in each group). (H) Representative immunoblots with respective proteins from the total lysates of mouse heart tissues isolated from indicated mouse heart tissues. Expression levels were normalized to loading control and presented as relative expression levels compared with the level in NTg-NSF mouse heart tissues. Gapdh levels were used as a loading control. Values are shown as means ± SEM with each experiment performed in triplicate (n = 3 in each group). Significance was evaluated by Student’s t test or one-way analysis of variance (ANOVA) with post hoc sidak multiple comparison test, respectively. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
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    Levels of the following enzyme activity are represented a) Acid Phosphatase (ACP) in unit/mL, b) Creatine Kinase (CK) in ng/mL, c) Glucose-6-Phosphate Dehydrogenase (G6PD) in ng/mL and d) Sorbitol Dehydrogenase (SDH) in mIU/mL. Values are given as mean ± SEM, for ten rats per group. Values are statistically significant at * p <0.05.

    Journal: PLOS ONE

    Article Title: Effects of empagliflozin on gonadal functions of hyperglycemic male wistar rats

    doi: 10.1371/journal.pone.0305636

    Figure Lengend Snippet: Levels of the following enzyme activity are represented a) Acid Phosphatase (ACP) in unit/mL, b) Creatine Kinase (CK) in ng/mL, c) Glucose-6-Phosphate Dehydrogenase (G6PD) in ng/mL and d) Sorbitol Dehydrogenase (SDH) in mIU/mL. Values are given as mean ± SEM, for ten rats per group. Values are statistically significant at * p <0.05.

    Article Snippet: Acid phosphatase (ACP) (Abcam, USA, cat. # ab83367), glucose-6-phosphate dehydrogenase (G6PD) (MyBiosource, USA, cat. # MBS2702342), sorbitol dehydrogenase (SDH) (MyBiosource, USA, cat. # MBS166115) and Seminal Creatine Kinase (MyBiosource, USA, cat. # MBS1600481) activities in the rats’ testis tissue homogenate was measured according to the instructions of the kit’s manufacturer.

    Techniques: Activity Assay

    SF alters redox homeostasis (A) Reduced glutathione (GSH) levels, (B) oxidized glutathione (GSSG) levels and (C) GSH/GSSG ratio in mouse heart tissues isolated from NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF, respectively, were measured by enzymatic recycling method. (D) Glucose-6-phosphate dehydrogenase (G6PD) activity, (E) catalase activity and (F) malondialdehyde levels measured in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. (G) Quantitative RT-PCR analysis of redox regulating genes ( Nrf2 , Nqo1 , Gclm , Gsr , Gsta , G6pd , Cat , Sod1 , and Sod2 ) in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. mRNA levels were normalized to Gapdh and presented as relative expression levels compared to level in NTg-NSF mouse heart tissues. Values are mean ± SEM. with each experiment performed in triplicates (n = 6 in each group). (H) Representative immunoblots with respective proteins from the total lysates of mouse heart tissues isolated from indicated mouse heart tissues. Expression levels were normalized to loading control and presented as relative expression levels compared with the level in NTg-NSF mouse heart tissues. Gapdh levels were used as a loading control. Values are shown as means ± SEM with each experiment performed in triplicate (n = 3 in each group). Significance was evaluated by Student’s t test or one-way analysis of variance (ANOVA) with post hoc sidak multiple comparison test, respectively. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001. See also <xref ref-type=Figure S2 . " width="100%" height="100%">

    Journal: iScience

    Article Title: Sleep fragmentation induces heart failure in a hypertrophic cardiomyopathy mouse model by altering redox metabolism

    doi: 10.1016/j.isci.2024.109075

    Figure Lengend Snippet: SF alters redox homeostasis (A) Reduced glutathione (GSH) levels, (B) oxidized glutathione (GSSG) levels and (C) GSH/GSSG ratio in mouse heart tissues isolated from NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF, respectively, were measured by enzymatic recycling method. (D) Glucose-6-phosphate dehydrogenase (G6PD) activity, (E) catalase activity and (F) malondialdehyde levels measured in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. (G) Quantitative RT-PCR analysis of redox regulating genes ( Nrf2 , Nqo1 , Gclm , Gsr , Gsta , G6pd , Cat , Sod1 , and Sod2 ) in NTg-NSF, NTg-SF, Tg-NSF, and Tg-SF mouse heart tissues. mRNA levels were normalized to Gapdh and presented as relative expression levels compared to level in NTg-NSF mouse heart tissues. Values are mean ± SEM. with each experiment performed in triplicates (n = 6 in each group). (H) Representative immunoblots with respective proteins from the total lysates of mouse heart tissues isolated from indicated mouse heart tissues. Expression levels were normalized to loading control and presented as relative expression levels compared with the level in NTg-NSF mouse heart tissues. Gapdh levels were used as a loading control. Values are shown as means ± SEM with each experiment performed in triplicate (n = 3 in each group). Significance was evaluated by Student’s t test or one-way analysis of variance (ANOVA) with post hoc sidak multiple comparison test, respectively. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001. See also Figure S2 .

    Article Snippet: Glucose-6-phosphate dehydrogenase (G6PD) activity: G6PD activity in the cardiac tissue lysates were determined by measuring reduced nicotinamide adenine dinucleotide (NADH) at 450 nm using a glucose-6-phosphate dehydrogenase assay kit (ab102529, Abcam) according to the manufacturer’s instructions.

    Techniques: Isolation, Activity Assay, Quantitative RT-PCR, Expressing, Western Blot, Comparison