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5 oxo 6e

Manufactured by Cayman Chemical
Sourced in Germany

5-oxo-6E is a research chemical compound commonly used in scientific laboratories. It serves as a precursor or intermediate in the synthesis of other compounds. The core function of 5-oxo-6E is to facilitate chemical reactions and transformations as part of the research and development process. No further details on its intended use are provided.

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2 protocols using 5 oxo 6e

1

Lipid Standards for Targeted Lipidomics

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The following lipid standards were purchased from Cayman Chemical: 5-oxo-6E,8Z,11Z,14Z-eicosatetraenoic-6,8,9,11,12,14,15-d7 acid (5-oxoETE-d7, ≥99% deuterated product), 17-oxo-4Z,7Z,10Z,13Z,15E,19Z-docosahexaenoic acid (17-oxo-DHA, ≥98%), 17-oxo-7Z,10Z,13Z,15E,19Z-docosapentaenoic acid (17-oxo-DPA, ≥98%), (±)13-hydroxy-4Z,7Z,10Z,14E,16Z,19Z-docosahexaenoic acid (13-OH-DHA, >98%), (±)7-hydroxy-4Z,8E,10Z,13Z,16Z,19Z-docosahexaenoic acid (7-OH-DHA, >98%), 5-oxo-6E,8Z,11Z,14Z-eicosatetraenoic acid (5-oxoETE, >95%), 5S-hydroxy-6E,8Z,11Z,14Z-eicosatetraenoic acid (5-OH-ETE, >98%), (±)-5-hydroxy-6E,8Z,11Z,14Z,17Z-eicosapentaenoic acid (5-OH-EPA, >98%). Docosahexaenoic acid (DHA, >99%) and docosapentaenoic acid (DPA, >99%) were purchased from NuCheck Prep, Inc.
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2

Neutrophil Biochemical Assays Protocol

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The chemicals were obtained from the following sources: aminophenyl fluorescein (APF) and HPLC-standards 5S-hydroperoxy-6E,8Z,11Z,14Z-eicosatetraenoic acid (5-HpETE), 5Shydroxy-6E,8Z,11Z,14Z-eicosatetraenoic acid (5-HETE), 5S,12R-dihydroxy-6E,8E,10E,14Zeicosatetraenoic acid (5,12-DiHETE), 5-oxo-6E,8Z,11Z,14Z-eicosatetraenoic acid (5-oxo-ETE), LTB4, prostaglandin B2 (PGB2) and AA were from Cayman Chemical (distributed by Biomol, Hamburg, Germany); HPLC solvents were from Carl Roth (Karlsruhe, Germany); glutathione colorimetric detection kit from Arbor Assays (Ann Arbor, Michigan, United States); biocoll (10 mM HEPES, 1.077 g/l, isotone) from Biochrom (Berlin, Germany) and all other chemicals including the JC-1 staining kit (CS0390) were from Sigma (Taufkirchen, Germany).
Working solutions of H2O2 were prepared by dilution of the corresponding stock solutions. Their concentrations were determined spectrophotometrically using ε240 = 43.6 M -1 cm -1 [Beers and Sizer 1952 ]. The buffer system hanks' balanced salt solution (HBSS) with and without Ca 2+ for the resuspension of neutrophils was prepared daily and adjusted to pH 7.4.
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