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Cell lysis solution

Manufactured by Keygen Biotech
Sourced in China

The Cell Lysis Solution is a reagent designed to disrupt the cell membrane and release the cellular contents, including proteins, nucleic acids, and other biomolecules. It is a key component in various biological and biochemical applications that require the extraction and isolation of cellular components.

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2 protocols using cell lysis solution

1

Neuroprotective Potential of Natural Compounds

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Ringer's solution, containing 122 mM sodium chloride, 3 mM potassium chloride, 0.4 mM monopotassium phosphate, 1.2 mM magnesium sulfate, 25 mM sodium bicarbonate, and 1.2 mM calcium chloride, was purchased from Millipore (MA, USA). Pachymic acid, liquiritin, rhynchophylline, isorhynchophylline, corynoxeine, and isocorynoxeine (purity ≥ 99%) were purchased from National Institutes for Food and Drug Control (Beijing, China). Fetal bovine serum (FBS) was purchased from Gibco/BRL (Grand Island, NY, USA). Methyl thiazolyl tetrazolium (MTT), dimethyl sulfoxide (DMSO), and trypsin were provided by Sigma Chemical (St. Louis, MO, USA). Aβ1–42 (purity ≥ 95%) was purchased from Abcam (Cambridge, USA). HPLC-grade acetonitrile was purchased from Thermo Fisher Scientific (Massachusetts, USA). EliVision plus and DAB kits were provided by Fuzhou Maixin Biotech. Co., Ltd. (Fuzhou, China). Bax, Bcl-2, caspase-3 and caspase-9 antibodies, annexin V-FITC/PI assay kit, basal DMEM medium, cell lysis solution, and 0.1% DEPC water were purchased from Nanjing KeyGen Biotech Co., Ltd. (Nanjing, China). Nimodipine was provided by Bayer healthcare Co., Ltd. (Leverkusen, Germany).
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2

Protein Expression Analysis Protocol

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Cell lysis solution (Nanjing KeyGen Biotech Co., Ltd, Nanjing, China) was added, the dish agitated for 30 min, centrifuged at 12,000 × g at 4°C for 15 min and the supernatant removed. Detection of protein concentration was conducted using BCA protein quantitative kits. Protein extracts (20 µg) were separated by 8–10% SDS polyacrylamide gel electrophoresis, then transferred to nitrocellulose membranes and blocked by 10% skim milk for 1.5 h at 4°C, then incubated by the corresponding antibody at 4°C overnight (HIF-1α, 1:1,000; Twist, 1:500; E-cad, 1:200; N-cad, 1:1,000; and β-actin, 1:1,500), β-actin was used as an internal control. The second antibody incubation was at room temperature for 1 h, followed by ECL chemiluminescence reagent chromogenic (cat. no. MA02454; Thermo Fisher Scientific, Inc.) for 1 min and exposure in an Amersham Imager 600 instrument (GE Healthcare Life Sciences, Little Chalfont, UK). This was followed with grey value analysis with Quantity one, the relative grayscale value indicating the corresponding protein expression level.
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