nadh1 Search Results


nadh dehydrogenase subunit 1 nd1  (Proteintech)
94
Proteintech nadh dehydrogenase subunit 1 nd1
A CYP2E1 protein expression and B Immunohistochemical staining of NAPQI-protein adducts were performed, and the images were captured at a 100 µm scale bar. C The mtDNA/nDNA content and D the expression of <t>ND1,</t> TFAM, and CYTB were measured in the liver tissues after 3 h of PBS or APAP supplementation. E Total liver GSH levels were also determined. F Cytoplasmic and mitochondrial proteins from 293 T cells were isolated, and AIM2 was analyzed through western blotting. β-tubulin and VDAC1 served as markers for the cytoplasm (Cy) and mitochondria (Mi), respectively. “Wh” designates the whole lysate. G Co-localization analysis of AIM2 and mitochondria in 293 T cells. AIM2 is highlighted in green, mitochondria in red, DAPI in blue, and co-localized regions are depicted in yellow. Scale bars, 10 µm. H TUNEL staining was conducted 24 h after APAP injection, and the images were captured at a 100 µm scale bar. I The serum IL-6 level and J the relative hepatic mRNA levels were measured in WT and AIM2 −/− mice at 24 h after APAP supplementation. Each group consisted of six mice per time point. Statistical analysis indicated no significance (Ns), * P < 0.05, ** P < 0.01, and *** P < 0.001.
Nadh Dehydrogenase Subunit 1 Nd1, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nadh1/pmc10907373-257-17-26?v=Proteintech
Average 94 stars, based on 1 article reviews
nadh dehydrogenase subunit 1 nd1 - by Bioz Stars, 2026-08
94/100 stars
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bidirectional sequencing of the cox1 and nadh1 genes  (CinnaGen Co)
90
CinnaGen Co bidirectional sequencing of the cox1 and nadh1 genes
A CYP2E1 protein expression and B Immunohistochemical staining of NAPQI-protein adducts were performed, and the images were captured at a 100 µm scale bar. C The mtDNA/nDNA content and D the expression of <t>ND1,</t> TFAM, and CYTB were measured in the liver tissues after 3 h of PBS or APAP supplementation. E Total liver GSH levels were also determined. F Cytoplasmic and mitochondrial proteins from 293 T cells were isolated, and AIM2 was analyzed through western blotting. β-tubulin and VDAC1 served as markers for the cytoplasm (Cy) and mitochondria (Mi), respectively. “Wh” designates the whole lysate. G Co-localization analysis of AIM2 and mitochondria in 293 T cells. AIM2 is highlighted in green, mitochondria in red, DAPI in blue, and co-localized regions are depicted in yellow. Scale bars, 10 µm. H TUNEL staining was conducted 24 h after APAP injection, and the images were captured at a 100 µm scale bar. I The serum IL-6 level and J the relative hepatic mRNA levels were measured in WT and AIM2 −/− mice at 24 h after APAP supplementation. Each group consisted of six mice per time point. Statistical analysis indicated no significance (Ns), * P < 0.05, ** P < 0.01, and *** P < 0.001.
Bidirectional Sequencing Of The Cox1 And Nadh1 Genes, supplied by CinnaGen Co, 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/product/nadh1/pmc12004059-59-6-16?v=CinnaGen+Co
Average 90 stars, based on 1 article reviews
bidirectional sequencing of the cox1 and nadh1 genes - by Bioz Stars, 2026-08
90/100 stars
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nadh 1  (SERVA Electrophoresis)
90
SERVA Electrophoresis nadh 1
A CYP2E1 protein expression and B Immunohistochemical staining of NAPQI-protein adducts were performed, and the images were captured at a 100 µm scale bar. C The mtDNA/nDNA content and D the expression of <t>ND1,</t> TFAM, and CYTB were measured in the liver tissues after 3 h of PBS or APAP supplementation. E Total liver GSH levels were also determined. F Cytoplasmic and mitochondrial proteins from 293 T cells were isolated, and AIM2 was analyzed through western blotting. β-tubulin and VDAC1 served as markers for the cytoplasm (Cy) and mitochondria (Mi), respectively. “Wh” designates the whole lysate. G Co-localization analysis of AIM2 and mitochondria in 293 T cells. AIM2 is highlighted in green, mitochondria in red, DAPI in blue, and co-localized regions are depicted in yellow. Scale bars, 10 µm. H TUNEL staining was conducted 24 h after APAP injection, and the images were captured at a 100 µm scale bar. I The serum IL-6 level and J the relative hepatic mRNA levels were measured in WT and AIM2 −/− mice at 24 h after APAP supplementation. Each group consisted of six mice per time point. Statistical analysis indicated no significance (Ns), * P < 0.05, ** P < 0.01, and *** P < 0.001.
Nadh 1, supplied by SERVA Electrophoresis, 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/product/nadh1/pm20390544-163-9-11?v=SERVA+Electrophoresis
Average 90 stars, based on 1 article reviews
nadh 1 - by Bioz Stars, 2026-08
90/100 stars
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nadh/[1]2+/xtt  (Chemie GmbH)
90
Chemie GmbH nadh/[1]2+/xtt
A CYP2E1 protein expression and B Immunohistochemical staining of NAPQI-protein adducts were performed, and the images were captured at a 100 µm scale bar. C The mtDNA/nDNA content and D the expression of <t>ND1,</t> TFAM, and CYTB were measured in the liver tissues after 3 h of PBS or APAP supplementation. E Total liver GSH levels were also determined. F Cytoplasmic and mitochondrial proteins from 293 T cells were isolated, and AIM2 was analyzed through western blotting. β-tubulin and VDAC1 served as markers for the cytoplasm (Cy) and mitochondria (Mi), respectively. “Wh” designates the whole lysate. G Co-localization analysis of AIM2 and mitochondria in 293 T cells. AIM2 is highlighted in green, mitochondria in red, DAPI in blue, and co-localized regions are depicted in yellow. Scale bars, 10 µm. H TUNEL staining was conducted 24 h after APAP injection, and the images were captured at a 100 µm scale bar. I The serum IL-6 level and J the relative hepatic mRNA levels were measured in WT and AIM2 −/− mice at 24 h after APAP supplementation. Each group consisted of six mice per time point. Statistical analysis indicated no significance (Ns), * P < 0.05, ** P < 0.01, and *** P < 0.001.
Nadh/[1]2+/Xtt, supplied by Chemie GmbH, 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/product/nadh1/pm40095709-116-19-59?v=Chemie+GmbH
Average 90 stars, based on 1 article reviews
nadh/[1]2+/xtt - by Bioz Stars, 2026-08
90/100 stars
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Image Search Results


A CYP2E1 protein expression and B Immunohistochemical staining of NAPQI-protein adducts were performed, and the images were captured at a 100 µm scale bar. C The mtDNA/nDNA content and D the expression of ND1, TFAM, and CYTB were measured in the liver tissues after 3 h of PBS or APAP supplementation. E Total liver GSH levels were also determined. F Cytoplasmic and mitochondrial proteins from 293 T cells were isolated, and AIM2 was analyzed through western blotting. β-tubulin and VDAC1 served as markers for the cytoplasm (Cy) and mitochondria (Mi), respectively. “Wh” designates the whole lysate. G Co-localization analysis of AIM2 and mitochondria in 293 T cells. AIM2 is highlighted in green, mitochondria in red, DAPI in blue, and co-localized regions are depicted in yellow. Scale bars, 10 µm. H TUNEL staining was conducted 24 h after APAP injection, and the images were captured at a 100 µm scale bar. I The serum IL-6 level and J the relative hepatic mRNA levels were measured in WT and AIM2 −/− mice at 24 h after APAP supplementation. Each group consisted of six mice per time point. Statistical analysis indicated no significance (Ns), * P < 0.05, ** P < 0.01, and *** P < 0.001.

Journal: Cell Death Discovery

Article Title: AIM2 regulates autophagy to mitigate oxidative stress in aged mice with acute liver injury

doi: 10.1038/s41420-024-01870-2

Figure Lengend Snippet: A CYP2E1 protein expression and B Immunohistochemical staining of NAPQI-protein adducts were performed, and the images were captured at a 100 µm scale bar. C The mtDNA/nDNA content and D the expression of ND1, TFAM, and CYTB were measured in the liver tissues after 3 h of PBS or APAP supplementation. E Total liver GSH levels were also determined. F Cytoplasmic and mitochondrial proteins from 293 T cells were isolated, and AIM2 was analyzed through western blotting. β-tubulin and VDAC1 served as markers for the cytoplasm (Cy) and mitochondria (Mi), respectively. “Wh” designates the whole lysate. G Co-localization analysis of AIM2 and mitochondria in 293 T cells. AIM2 is highlighted in green, mitochondria in red, DAPI in blue, and co-localized regions are depicted in yellow. Scale bars, 10 µm. H TUNEL staining was conducted 24 h after APAP injection, and the images were captured at a 100 µm scale bar. I The serum IL-6 level and J the relative hepatic mRNA levels were measured in WT and AIM2 −/− mice at 24 h after APAP supplementation. Each group consisted of six mice per time point. Statistical analysis indicated no significance (Ns), * P < 0.05, ** P < 0.01, and *** P < 0.001.

Article Snippet: Antibodies against Cytochrome b (CYTB) (#55090-1-AP), Mitochondrial transcription factor A (TFAM) (#22586-1-AP), VDAC (#55259-1-AP), tubulin (#11224-1-AP), and NADH dehydrogenase subunit 1 (ND1) (#19,703-1-AP), were obtained from Proteintech Group, Inc (Wuhan, China).

Techniques: Expressing, Immunohistochemical staining, Staining, Isolation, Western Blot, TUNEL Assay, Injection