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L arginine

Manufactured by Solarbio
Sourced in China

L-arginine is an amino acid that is essential for various biological processes in the body. It serves as a precursor for the synthesis of proteins and plays a role in the production of nitric oxide, which is important for cardiovascular function. L-arginine is commonly used in laboratory settings for research and experimental purposes.

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3 protocols using l arginine

1

Bacterial Amino Acid Decarboxylase Assay

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Production of BAs was tested by inoculating isolates (7–9 log CFU ml–1) directly into tubes containing 10 ml of mixed amino acid decarboxylase media. The medium described by Møller (1954) (link) was used to culture the enteric bacteria. The media were supplemented with L-histidine, L-lysine, L-arginine, and L-tyrosine at 0.5% final concentration and L-ornithine monohydrochloride (Solarbio, China) at 0.25% final concentration. Pyridoxal-5-phosphate (Macklin, China) was included in the media (at 0.005%).
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2

Calycosin Ameliorates Inflammatory Response

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L-arginine (L-arg: purity > 98%, endotoxin-free) and the BCA Protein Assay Kit were purchased from Beijing Solarbio Science and Technology Co., Ltd. (Beijing, China). Calycosin (Cal: C16H12O5, purity > 98%;) was from Chengdu Biopurify Phytochemicals Ltd. (Chengdu, China). Enzyme-linked immunosorbent assay (ELISA) kits for interleukin (IL)-6, HMGB1, IL-1β and MPO were obtained from Wuhan Cloud-Clone Corp. (Wuhan, China). ELISA kits for tumor necrosis factor (TNF)-α and CXCX-1 were procured from Proteintech Group (Rosemont, IL, United States). The amylase ELISA kit was bought from Shanghai BlueGene Biotech Co., Ltd. (Shanghai, China). Primary antibodies against NF-κB p65 (p65), phosphorylated NF-κB p65 (p-p65), and GAPDH were purchased from Cell Signaling Technology Inc. (Danvers, MA, United States). Primary antibody against lymphocyte antigen 6 complex locus G6D (Ly6G) was obtained from Abcam (Cambridge, United Kingdom). Primary antibody against HMGB1 and Fluorescent secondary antibody were produced by Proteintech Group. Horseradish peroxidase (HRP)-conjugated secondary antibodies and Hypersensitive WB Chemiluminescent Substrate Reagent were from Beyotime Biotechnology (Jiangsu, China).
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3

Evaluating Candida albicans Proliferation

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C. albicans were treated with 15 μg/mL EVs from YNB or PBS control in different medium at 37 °C for 24 h. The influence of different amino acids on promoting proliferative effects was tested in 0.2% glucose YNB and YPD media in addition of 0.02%, 0.05%, 0.1%, 0.2%, 0.3% l-arginine, 0.2% l-cysteine, 0.2% l-proline, 0.2% l-leucine, 0.2% l-isoleucine, 0.2% l-valine, 0.2% l-methionine, 0.2% l-glutamic acid, 0.2% l-ornithine, 0.2% l-citrulline, and 0.2% l-histidine, respectively (all the amino acids were from Solarbio, Beijing, China). The influence of different glucose concentrations on promoting proliferative effects was tested using media including in RPMI 1640 medium with the addition of 0.2%, 2% glucose, and YNB medium in addition of 0.2%, 0.4%, 0.8%, and 2% glucose, respectively. The influence of oxidants and antioxidants on promoting proliferative effects was tested using media including 0.2% glucose YNB with 0.25 mM, 0.5 mM H2O2 (Boster, Wuhan, China) or 0.125 mM, and 0.25 mM glutathione (GSH) (Solarbio, Beijing, China). After being mixed in 96-well plates, C. albicans cells were serially diluted with PBS; then, 150 μL of C. albicans dilutions was spread on YPD plates. After 12 h of culture at 37 °C, the CFUs were counted. All the experiments were repeated in triple.
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