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8s hete

Manufactured by Cayman Chemical
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Sourced in United States

8S-HETE is a biochemical compound produced and sold by Cayman Chemical. It is a hydroxyeicosatetraenoic acid (HETE) that functions as a bioactive lipid mediator. The core function of 8S-HETE is to serve as a scientific research tool for the study of eicosanoid biology and signaling pathways.

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Lab products found in correlation

Stearidonic acid, by Cayman Chemical (1 mentions) 8 hepe, by Cayman Chemical (1 mentions) Pfastbac vector, by Thermo Fisher Scientific (1 mentions) 8s hepe, by Cayman Chemical (1 mentions) 8 hete, by Cayman Chemical (1 mentions) Spodoptera frugiperda sf9 insect cells, by Thermo Fisher Scientific (1 mentions) Docosapentaenoic acid dpa, by Cayman Chemical (1 mentions) Arachidonic acid, by Cayman Chemical (1 mentions) Taurochenodeoxycholate, by Merck Group (1 mentions) Lysophosphatidylcholine, by Merck Group (1 mentions) 12 r hete, by Cayman Chemical (1 mentions) Glycocholic acid, by Santa Cruz Biotechnology (1 mentions) Octanoyl carnitine, by Cayman Chemical (1 mentions)

2 protocols using 8s hete

1

Recombinant Eicosanoid Production

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ARA, EPA, and DHA were purchased from Nacalai Tesque (Kyoto, Japan). (±)8-HEPE (comprising equal amounts of 8S-HEPE and 8R-HEPE), 8S-HEPE, (±)8-HETE, 8S-HETE, 8R-HETE, rac-10-HDHA, PD1, gamma-linoleic acid (GLA), stearidonic acid (SDA) and docosapentaenoic acid (DPA) were purchased from Cayman Chemical Company (Ann Arbor, MI, USA). The Spodoptera frugiperda (Sf9) insect cells, and pFastBac vector were purchased from Thermo Fisher Scientific (Franklin, MA, USA). The anti-6xHis antibody [HIS.H8] was purchased from Abcam Japan (Tokyo, Japan).
Yuki S., Uemura A., Hakozaki M., Yano A., Abe M., Misawa Y., Baba N, & Yamada H. (2020). Identification of a novel enzyme from E. pacifica that acts as an eicosapentaenoic 8R-LOX and docosahexaenoic 10R-LOX. Scientific Reports, 10, 20592.
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2

Metabolite Confirmation Standards for Research

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Chemical standards utilized for the confirmation of identified metabolites included glycocholic acid (sc-218574), glycoursodeoxycholate (sc-211567), and glycolithocholate (sc-396741) (Santa Cruz Biotechnology, Inc., Dallas, TX, USA); glycochenodeoxycholate (16942), taurodeoxycholate (15935), acetylcarnitine (16948), octanoylcarnitine (15048), prostaglandin B2 (11210), 12-oxo-leukotriene B4 (20140), arachidonic acid (90010), 12(R)-HETE (34560), 8(S)-HETE (34360) and lyso-PAF (C18) (60916) from Cayman Chemical (Ann Arbor, Michigan, USA); glycodeoxycholate (G9910), taurochenodeoxycholate (T6260), lysophosphatidylcholine (L4129) and from Sigma-Aldrich (St. Louis, MO, USA); and Sphingomyelin mixture (860061,2,3, Avanti Polar Lipids, Inc., Alabaster, Alabama, USA).
Fitzgerald B.L., Molins C.R., Islam M.N., Graham B., Hove P.R., Wormser G.P., Hu L., Ashton L.V, & Belisle J.T. (2020). Host Metabolic Response in Early Lyme Disease. Journal of proteome research, 19(2), 610-623.
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