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Triglyceride tg colorimetric assay kit

Manufactured by Elabscience
Sourced in China

The Triglyceride (TG) Colorimetric Assay Kit is a laboratory tool used to quantify the concentration of triglycerides in samples. It provides a colorimetric method for the detection and measurement of triglycerides.

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4 protocols using triglyceride tg colorimetric assay kit

1

Triglyceride Quantification in Flies

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Ten larvae or flies (one sample) were homogenized in 150 μL cold isopropanol. The homogenized samples were then centrifuged at 12,000 g for 10 min at 4 ℃. Next, triglyceride (TAG) levels were assayed using the Triglyceride (TG) Colorimetric Assay Kit (Elabscience) according to the manual. Protein contents were determined by the BCA Protein Quantification Kit for normalization.
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2

Evaluation of NASH therapeutic compounds

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CS271011 was designed and synthesized at Chipscreen Biosciences (Shenzhen, Guangdong, China). The purity of CS271011 was over 99%. Resmetirom (MGL-3196) was purchased from MedChemExpress (Hycultec GmbH, Beutelsbach, Germany). Compounds were dissolved and suspended in sterile DMSO and 0.2% CMC-Na for in vitro and in vivo administration, respectively. The chow diet was supplied by Guangdong Medical Laboratory Animal Center (Foshan, Guangdong, China), and the high-fat diet (D12492i) was provided by SYSE Biotech Co., Ltd. (Changzhou, Jiangsu, China). Cholesterol (TC), alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP), and total bilirubin (TBIL) diagnostic kits were purchased from the Jiancheng Bioengineering Institute of Nanjing (Nanjing, Jiangsu, China). The Triglyceride (TG) Colorimetric Assay Kit was purchased from Elabscience (Wuhan, Hubei, China). All primers were synthesized by Genewiz (Suzhou, Jiangsu, China).
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3

Triglyceride Assay in HK-2 Cells

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HK-2 cells were inoculated in 6-well plates at 5 × 105 cells per well. We treated cells with TPA for 48 h with or without rklotho. At the end of treatment, cells were broken using Scientz-IID Ultrasonic Cell Crusher (Scientz, China), and the cell supernatants were collected for triglyceride measurement. Triglyceride concentrations in cell supernatants were determined using a triglyceride (TG) colorimetric assay kit (Elabscience, China) according to the manufacturer's instructions.
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4

Triglyceride Quantification in C. elegans

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Sample processing for triglyceride quantification was performed as described in Werthebach et al. (2019) [73 ]. Briefly, three to six crawling L3 larvae were transferred in a 1.5-mL Eppendorf tube and homogenised in 100 μL 0.05% Tween20 in H2O per larva, using a motorised homogeniser. Then, the homogenate was heat inactivated by incubation at 70 °C for 5 min and centrifuged at 5000 rpm for 5 min. The supernatant was collected in a new tube and centrifuged at 14,800 rpm for 15 min at 4 °C. Triglyceride measurement was performed using the Triglyceride (TG) Colorimetric Assay Kit (Elabscience, USA) according to the manufacturer’s instructions. Protein values used to normalise TG measurements were quantified using the Bradford method. Both male and female larvae samples were collected and following comparison of TG levels with no sex-specific changes found, male and female measurements were pooled.
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