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Catalase activity assay kit

Manufactured by Cayman Chemical
Sourced in United States

The Catalase Activity Assay Kit is a laboratory tool designed to measure the activity of the catalase enzyme. Catalase is an important antioxidant enzyme found in most living organisms that catalyzes the decomposition of hydrogen peroxide into water and oxygen. The kit provides a quantitative colorimetric method to determine catalase activity in various sample types.

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4 protocols using catalase activity assay kit

1

Catalase Activity Assay in Cell Extract

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Catalase activity in the crude cell extract was determined using a Catalase Activity Assay kit (Cayman Chemical, Ann Arbor, MI, USA) following the manufacturer’s instructions.
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2

Coagonist Peptide Synthesis and Analysis

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The coagonist of GCGR and GLP-1R, Aib2 C24 Chimera2 (H1SQGT5FTSDY10SKYLD15EQAAK20EFIAW25LMNT-NH2) was synthesized at Zydus Research Centre, Ahmedabad, India[20 (link)]. Kits for triglycerides, cholesterol, and glucose were purchased from Avantor Performance Materials India Ltd, India. ELISA kits for IL-6 and TNF-α were obtained from BD Biosciences, United States; Insulin from Crystal Chem, United States; FGF21 from Wuhan Eiaab science, Co., Ltd. China; leptin and Adiponectin were purchased from B-bridge international, United States. Superoxide dismutase (SOD) and catalase activity assay kit were obtained from Cayman Chemical, United States. Creatinine, blood urea nitrogen, and albumin assay kit were obtained from Sigma-Aldrich, United States. TRIzol reagent and cDNA reverse transcription kit purchased from Invitrogen, Life Technology, United States and QIAGEN Quanti Fast SYBR Green kit were purchased from Qiagen, Germantown, United States. All other chemicals and reagents were purchased from Sigma-Aldrich chemicals, United States unless stated otherwise.
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3

Antioxidant Enzyme Activity Measurement

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The activities of catalase, SOD, and GPx were measured using catalase activity assay kit (Cayman Chemical, Ann Arbor, MI, USA), superoxide dismutase activity assay kit (Cayman Chemical), and glutathione peroxidase activity kit (Abcam), respectively. NHDF cells were seeded in 100-mm dishes at a density of 5 × 105 cells. Cells were pretreated or not pretreated with each conditioned medium (1×) for 24 h, followed by exposure to 600 μM H2O2 for 2 h. The reaction was processed according to the manufacturer’s protocol. Activities of catalase, superoxide dismutase, and glutathione peroxidase were measured at 540, 440, and 340 nm, respectively.
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4

Liver Antioxidant Enzyme Activity Analysis

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Liver tissue lysates were subjected to a GSH assay kit (Cayman Chemical, # 703002, Ann Arbor, MI, USA) and a GSH Px assay kit (Abcam ab102530, USA) according to the manufacturer's instructions as previously described [31] . To determine the manganese superoxide dismutase (MnSOD) activity, aliquots of liver lysates were treated with CuZnSOD inhibitor and then subjected to a commercial superoxide dismutase (SOD) assay kit (Cayman Chemical, # 706002, Ann Arbor, MI, USA) according to the manufacturer's instructions. Catalase activity was measured using a commercial catalase activity assay kit (Cayman Chemical, # 707002, Ann Arbor, MI, USA) according to the manufacturer's instructions as previously described [31] .
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