Serum Triglyceride Measurement

ZH Zsófia Hoyk
MT Melinda E. Tóth
NL Nikolett Lénárt
DN Dóra Nagy
BD Brigitta Dukay
AC Alexandra Csefová
ÁZ Ágnes Zvara
GS György Seprényi
AK András Kincses
FW Fruzsina R. Walter
SV Szilvia Veszelka
JV Judit Vígh
BB Beáta Barabási
AH András Harazin
ÁK Ágnes Kittel
LP László G. Puskás
BP Botond Penke
LV László Vígh
MD Mária A. Deli
MS Miklós Sántha
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Serum triglyceride levels in 7, 9, and 12-month-old APOB-100 transgenic (n = 5) and wild-type mice (n = 5) fed on a normal chow diet were measured using a colorimetric assay (Supplementary Table S1). Blood samples were collected through cardiac puncture under terminal anesthesia. After clot formation samples were centrifuged at 4°C, 1000 × g for 10 min, then serum was removed and stored at -80°C until use. Serum triglyceride levels were measured in triplicate using a commercially available enzymatic colorimetric assay kit (Diagnosticum Ltd., Budapest, Hungary) according to the manufacturer’s instructions. Test accuracy was monitored using Standard Lipid Controls (Diagnosticum Ltd., Budapest, Hungary). Absorbance of the produced purple color product was measured at 560 nm using a microplate reader (Multiskan FC, Thermo Scientific, United States). Values were expressed in mmol/liter. Experimental groups, (APOB-100 transgenic mice and wild-type littermates) consisted of 5 animals each.

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