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Abca1

Manufactured by Bioneer

ABCA1 is a laboratory equipment product designed for the detection and analysis of the ABCA1 protein. ABCA1 is a membrane-bound transporter protein that plays a crucial role in the regulation of cellular cholesterol and phospholipid homeostasis. The ABCA1 equipment allows for the quantification and examination of ABCA1 expression levels in various biological samples, which can be useful for researchers studying lipid metabolism and related diseases.

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2 protocols using abca1

1

HepG2 Cell Culture and Characterization

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The HepG2 human
hepatocellular liver cell line was obtained from the Korea Research
Institute of Bioscience and Biotechnology (Daejeon, South Korea) and
grown in Eagle’s minimum essential medium (EMEM) containing
10% fetal bovine serum and 100 U/mL penicillin/streptomycin sulfate.
Cells were incubated in a humidified 5% CO2 atmosphere
at 37 °C. EMEM, penicillin, and streptomycin were purchased from
Hyclone (Logan, UT, USA). Bovine serum albumin (BSA) and 25-hydroxycholesterol
were purchased from Sigma-Aldrich (St. Louis, MO, USA). 4′,6-Diamidino-2-phe-nylindole
(DAPI) and DiI-LDL were purchased from Thermo Fisher Scientific (Waltham,
MA, USA). Antibodies against LSS, SREBP1, SREBP2, HMGCR, SQLE, and
β-actin were purchased from Abcam, Inc. (Cambridge, MA, USA).
Antibodies against PCSK9 were purchased from Cell Signaling Technology.
(Beverly, MA, USA). SREBF1, SREBF2, HMGCR, PCSK9, IDI1, SQLE, ABCA1,
ACSL6, DHCR7, FDFT1, FDPS, SOAT1, and glyceraldehyde-3-phosphate dehydrogenase
(GAPDH) oligonucleotide primers were purchased from Bioneer Corp.
(Daejeon, South Korea). α-Mangostin was isolated from the chloroform
fraction of G. mangostana, as previously
described, and confirmed by a spectroscopic analysis. The purity of
α-mangostin was determined to be over 95% by high-performance
liquid chromatography using an ultraviolet detector.4 (link)
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2

Quantitative RT-PCR Analysis of Gene Expression

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Total RNA was isolated from HaCaT cells using TRIzol (Life Technologies, Carlsbad, CA, USA) according to the manufacturer’s protocol and a previously described method with a slight modification [17 (link)]. cDNA was synthesized from 1 µg RNA by a reverse transcriptional reaction. The qPCR amplification was performed with SYBR-Green/ROX qPCR Master Mix (2×) (BioFact Co., Daejeon, Republic of Korea). The PCR primers for IL-6, TNF-α, IL-1β, iNOS, PLTP, APOE, ABCA1, and GAPDH were obtained from Bioneer Corp. Primer sequences are listed in Table 1.
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