nadp Search Results


nadp nadph assay kit wst  (Dojindo Labs)
93
Dojindo Labs nadp nadph assay kit wst
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nadp nadph assay kit  (Elabscience Biotechnology)
94
Elabscience Biotechnology nadp nadph assay kit
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
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nadph tetrasodium salt  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology nadph tetrasodium salt
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
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me1  (Proteintech)
93
Proteintech me1
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
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beta nicotinamide adenine dinucleotide phosphate reduced tetrasodium salt nadph  (Thermo Fisher)
91
Thermo Fisher beta nicotinamide adenine dinucleotide phosphate reduced tetrasodium salt nadph
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
Beta Nicotinamide Adenine Dinucleotide Phosphate Reduced Tetrasodium Salt Nadph, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti idh2 rabbit pab  (Proteintech)
94
Proteintech anti idh2 rabbit pab
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
Anti Idh2 Rabbit Pab, 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
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idh1 antibody  (Proteintech)
94
Proteintech idh1 antibody
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
Idh1 Antibody, 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
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k242020 lr clonase enzyme mix thermo fisher scientific  (Addgene inc)
93
Addgene inc k242020 lr clonase enzyme mix thermo fisher scientific
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
K242020 Lr Clonase Enzyme Mix Thermo Fisher Scientific, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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nadph tetrasodium salt hydrate  (Thermo Fisher)
94
Thermo Fisher nadph tetrasodium salt hydrate
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
Nadph Tetrasodium Salt Hydrate, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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nadp  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology nadp
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
Nadp, 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
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β nicotinamide adenine dinucleotide phosphate disodium salt  (Thermo Fisher)
88
Thermo Fisher β nicotinamide adenine dinucleotide phosphate disodium salt
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
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nadp disodium salt  (Santa Cruz Biotechnology)
92
Santa Cruz Biotechnology nadp disodium salt
LINC01532 is identified as a potential <t>NADPH-metabolism-related</t> lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).
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Image Search Results


LINC01532 is identified as a potential NADPH-metabolism-related lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).

Journal: Journal of Advanced Research

Article Title: Long non-coding RNA LINC01532 sustains redox homeostasis and accelerates lenvatinib resistance in hepatocellular carcinoma

doi: 10.1016/j.jare.2025.02.035

Figure Lengend Snippet: LINC01532 is identified as a potential NADPH-metabolism-related lncRNA in HCC drug resistance. ( A ) The expression of G6PD, ME1, ME2 and MTHFD2 was analyzed in HCC tissues and adjacent non-cancerous tissues using TCGA dataset. ( B ) Venn diagram was employed to analyze the overlap lncRNAs among G6PD-related lncRNAs, prognosis related lncRNAs and differentially expressed lncRNAs. ( C ) The expression of the eight lncRNAs was evaluated by RT-qPCR in HCC tissues and the adjacent non-tumoral tissues from our hospital. ( D ) HuH-7 cells were transfected with indicated siRNAs and cellular NADPH level was determined. ( E ) The expression of eight lncRNAs was evaluated by RT-qPCR in lenvatinib-resistant HuH-7 cells. ( F ) The LINC01532 expression was analyzed in HCC tissues and adjacent non-tumoral tissues. ( G ) Overall survival (OS) and disease-free survival (DFS) analyses based on LINC01532 levels were analyzed using data from TCGA-LIHC cohort. ( H ) OS and DFS analyses based on LINC01532 level were analyzed using data from our cohort. ( I ) RT-qPCR was performed to detect LINC01532 expression in the cytoplasmic and nuclear fractions. ( J ) The subcellular localization of LINC01532 was determined by Fluorescence in situ hybridization (FISH). Scale bar, 10 μm. ( K ) LINC01532 coding capability was performed by CPAT ( http://lilab.research.bcm.edu ).

Article Snippet: NADPH, G6PD, GSH and MDA levels were evaluated using NADP + /NADPH Assay Kit (Beyotime, China), G6PDH Activity Assay Kit (Beyotime, China), Reduced Glutathione Content Assay Kit (Solarbio, China) and Malondialdehyde (MDA) Colorimetric Assay Kit (Elabscience, China), respectively, based on the manufacturer's protocol.

Techniques: Expressing, Quantitative RT-PCR, Transfection, Fluorescence, In Situ Hybridization

LINC01532 elevates PPP flux. ( A ) Cellular NADPH level was determined in HuH-7 and MHCC97-H stably overexpressing LINC01532. ( B ) Cellular G6PD activity was evaluated in the indicated cells. ( C ) Cellular NADPH level was detected in the indicated cells. ( D ) Cellular G6PD activity was determined in the indicated cells. ( E ) Cellular GSH level was assessed in HuH-7 and MHCC97-H stably overexpressing LINC01532. ( F ) Cellular GSH level was analyzed in the indicated cells. ( G ) Oil red O staining assay (left) was performed in the indicated cells. The numbers of lipid droplets around cells were summarized (n = 50, right). ( H ) Cellular NADPH level was determined in the indicated cells treated with RRX-001. ( I ) The indicated cells were treated with RRX-001 and cellular GSH level was determined. ( J ) Cellular NADPH level was determined in the cells transfected as indicated. ( K ) Oil red O staining (left) and statistical analysis (right) were performed in HuH-7 cells as indicated.

Journal: Journal of Advanced Research

Article Title: Long non-coding RNA LINC01532 sustains redox homeostasis and accelerates lenvatinib resistance in hepatocellular carcinoma

doi: 10.1016/j.jare.2025.02.035

Figure Lengend Snippet: LINC01532 elevates PPP flux. ( A ) Cellular NADPH level was determined in HuH-7 and MHCC97-H stably overexpressing LINC01532. ( B ) Cellular G6PD activity was evaluated in the indicated cells. ( C ) Cellular NADPH level was detected in the indicated cells. ( D ) Cellular G6PD activity was determined in the indicated cells. ( E ) Cellular GSH level was assessed in HuH-7 and MHCC97-H stably overexpressing LINC01532. ( F ) Cellular GSH level was analyzed in the indicated cells. ( G ) Oil red O staining assay (left) was performed in the indicated cells. The numbers of lipid droplets around cells were summarized (n = 50, right). ( H ) Cellular NADPH level was determined in the indicated cells treated with RRX-001. ( I ) The indicated cells were treated with RRX-001 and cellular GSH level was determined. ( J ) Cellular NADPH level was determined in the cells transfected as indicated. ( K ) Oil red O staining (left) and statistical analysis (right) were performed in HuH-7 cells as indicated.

Article Snippet: NADPH, G6PD, GSH and MDA levels were evaluated using NADP + /NADPH Assay Kit (Beyotime, China), G6PDH Activity Assay Kit (Beyotime, China), Reduced Glutathione Content Assay Kit (Solarbio, China) and Malondialdehyde (MDA) Colorimetric Assay Kit (Elabscience, China), respectively, based on the manufacturer's protocol.

Techniques: Stable Transfection, Activity Assay, Staining, Transfection