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Mpo from human leukocytes

Manufactured by Merck Group

MPO from human leukocytes is a laboratory product that provides a source of myeloperoxidase, an enzyme found in the granules of certain white blood cells. Myeloperoxidase is involved in the immune response and plays a role in the production of hypochlorous acid, which has antimicrobial properties. The product can be used for research and experimental purposes related to the study of myeloperoxidase and its functions.

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2 protocols using mpo from human leukocytes

1

Preparation and Characterization of Oxidants

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KYNA was purchased from ChemCruz (Dallas, TX). NaBr (>99.99%), NaCl (>99.99%), KH2PO4, K2HPO4, MPO from human leukocytes, and EPO human recombinant protein were purchased from Sigma-Aldrich (St. Louis, MO). Other chemicals were obtained from Nacalai Tesque (Kyoto, Japan) or TCI (Tokyo). Bromide-free hypobromous acid (HOBr) was prepared by the addition of silver nitrate and subsequent distillation, as previously reported.(21 (link)) The concentration of HOBr was determined spectrophotometrically at 331 nm in 10 mM NaOH using a molar extinction coefficient of 315 M−1 cm−1.(22 ) Chloride-free sodium hypochlorite (NaOCl) was prepared by the method previously reported.(23 (link)) The concentration of NaOCl was determined spectrophotometrically at 290 nm using a molar extinction coefficient of 350 M−1 cm−1.(24 )
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2

Synthetic Peptide Analysis Protocol

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Ultrapure water was used throughout the experiments except where otherwise stated. Trifluoroacetic acid (TFA), formic acid (FA), hydrogen peroxide (H2O2), phosphate buffered saline (PBS), acetonitrile (ACN), 2-propanol, methanol and ethyl acetate were obtained from Fisher Scientific (Pittsburgh, PA). Other chemicals, if not specified, were from Sigma-Aldrich (St. Louis, MO).
MPO from human leukocytes was also obtained from Sigma-Aldrich. Trypsin Gold was purchased from Promega (San Luis Obispo, CA). Synthetic peptides were produced and purified by GenScript (Piscataway, NJ) with three different sequences: peptide A - VLIYEDFKR; peptide B - VLIYEDFRR; peptide C - VLIFEDFKR. All three peptides were acetylated at the N-terminus and amidated at the C-terminus; the purity was ≥ 98 %.
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