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Sf1670

Manufactured by MedChemExpress
Sourced in United States

SF1670 is a laboratory instrument designed for the analysis and separation of chemical compounds. It utilizes a specialized technique called size exclusion chromatography to separate molecules based on their size and molecular weight. The core function of SF1670 is to facilitate the purification and isolation of target compounds from complex mixtures, enabling researchers to obtain high-purity samples for further analysis and experimentation.

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5 protocols using sf1670

1

Cultivation of Gastric Cell Lines

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Human gastric mucosa cell line (GES-1) used in this study was procured from BeNa Culture Collection (Beijing, China). Human GC cell lines (HGC-27, AGS) were bought from Cell Bank of the Chinese Academy of Sciences (Shanghai, China); both MKN-7 and MKN-45 cell lines were obtained from Procell Life Science & Technology Co., Ltd. (Wuhan, China). RPMI-1640 commercially acquired from Thermo Fisher Scientific (Waltham, MA) was used to culture GES-1, HGC-27, MKN-7, and MKN-45 cells under 37°C and 5% CO2. AGS cells were cultivated in F12K medium (Gibco). In addition, 10% fetal bovine serum (FBS; Gibco) and 1% penicillin-streptomycin (Gibco) both served as medium supplements. SF1670 (1 μM), an inhibitor of PTEN (phosphatase and tensin homolog), was purchased from MedChemExpress (South Brunswick, NJ).
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2

Purchasing LXR-623 and SF1670 from MedchemExpress

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LXR-623 and SF1670 were purchased from MedchemExpress (Monmouth Junction, NJ, USA).
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3

Lipid Peroxidation Inhibitor Screening

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Erastin, RSL-3, and necrostatin-1 (Ner-1) were purchased from Selleck Chemicals (Houston, USA). Tannic acid (TA), ferric chloride hexahydrate (FeCl3.6H2O), DMSO, and Ac-DEVD-CHO (Apo) were purchased from Macklin (Shanghai, China). EDTA and urea were purchased from Solarbio (Beijing, China). Fer-1, DFO, GSH, BSO, Liproxstatin-1, SF1670, and Chloroquine were purchased from MedChemExpress. Branched polyethyleneimine (PEI, Mw = 25,000) and 2′,7′-Dichlorofluorescin diacetate were purchased from Sigma-Aldrich. Antibodies against HA (MMS101P, Covance), FLAG (F1804, Sigma), UHRF1 (D6G8E, CST), HBP1 (11746-1-AP, Proteintech), CDO1 (12589–1 AP, Proteintech), PTEN (9188, CST), p-AKT (4060, CST), AKT (9272, CST), GPX4 (sc-166570, Santa cruz), ACSL4 (sc-365230, Santa cruz), TFRC (sc-32272, Santa cruz), β-actin (AC026, ABclonal). Rabbit anti-4-HNE antibody (Bioss). The following secondary antibodies were used: anti-mouse IgG antibody DyLight 800 (610-145-121, Rockland) and anti-rabbit IgG DyLight 800 (611-145-002, Rockland).
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4

Investigating the Role of Nrf2 in NOD Mice

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Non-obese diabetic (NOD) mice and Nrf2−/− mice were obtained from the Model Animal Research Center of Nanjing University (Nanjing, China). C57BL/6 mice were from Comparative Medical Center of Yangzhou University (Yangzhou, China). Experiments used 6–12-week-old and sex-matched mice, unless otherwise indicated. All animal care and handling procedures were conducted in accordance with the protocols approved by the Institutional Animal Care and Use Committee (IACUC) at Yangzhou University (Yangzhou, China).
The following reagents were used: Astilbin (HY-N0509); 1-aminobenzotriazole (ABT, HY-103389), a nonspecific and irreversible inhibitor of CYP enzymes; etomoxir (HY-50202), an inhibitor of CPT1α; SF1670 (HY-15842), an inhibitor of PTEN; N-Acetyl-L-cysteine (NAC, HY-B0215), a GSH-related antioxidant; GW9662 (HY-16578), a potent and selective PPARγ antagonist; and dorsomorphin (Compound C, HY-13418A), a selective and ATP-competitive AMPK inhibitor (MedChemExpress, NJ, United States).
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5

Naringenin Effects on RCC Cell Proliferation

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RCC cells were cultured with naringenin (0, 4 or 8 µm) for different periods of time (0, 24, 48, 72 or 96 h), or, after pretreatment with a PTEN inhibitor (SF1670, MedChemExpress)/activator (Oroxin B, MedChemExpress) for 24 h in a 37°C CO2 incubator, cells were treated with 4 µm naringenin for 24 h. Subsequently, cells were incubated with 10 µl CCK-8 at 37°C for 2–4 h. Finally, cell proliferation was determined by measurement of the absorbance at 450 nm on a spectrophotometer.
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