Category: Research kits

Reference: 19660-2,5
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A form of LPS extracted from wild-type S-form E. coli serotype O55:B5; commonly used to activate TLR4 on leukocytes, eliciting inflammatory signaling in isolated cells and in vivo
Reference: 10001-1
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This mixture contains the primary COX products produced by most mammalian tissues. Contents: Prostaglandin D2, Prostaglandin E2, 6-keto Prostaglandin F1α, Prostaglandin F2α, and Thromboxane B2 (100 µg each).
Reference: 10002-1
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This mixture contains primary prostaglandins produced from arachidonic acid and dihomo-γ-linolenic acid. Contents: Prostaglandin E1, Prostaglandin E2, Prostaglandin F1α, 6-keto Prostaglandin F1α, and Prostaglandin F2α...
Reference: 10004224-100
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A biologically active peroxidation product of linoleic acid; activates an ARE in neuronal cells and induces the expression of ARE-regulated cytoprotective genes; also stimulates the synthesis of aldosterone and...
Reference: 10004224-25
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A biologically active peroxidation product of linoleic acid; activates an ARE in neuronal cells and induces the expression of ARE-regulated cytoprotective genes; also stimulates the synthesis of aldosterone and...
Reference: 10004224-50
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A biologically active peroxidation product of linoleic acid; activates an ARE in neuronal cells and induces the expression of ARE-regulated cytoprotective genes; also stimulates the synthesis of aldosterone and...
Reference: 10004224-500
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A biologically active peroxidation product of linoleic acid; activates an ARE in neuronal cells and induces the expression of ARE-regulated cytoprotective genes; also stimulates the synthesis of aldosterone and...
Reference: 10004236-1
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An analog of fluprostenol 2-glyceryl ester with increased stability
Reference: 10004236-10
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An analog of fluprostenol 2-glyceryl ester with increased stability
Reference: 10004236-5
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An analog of fluprostenol 2-glyceryl ester with increased stability
Reference: 10004257-1
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A prominent autoxidation product of either trilinolein or arachidonic acid
Reference: 10004257-10
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A prominent autoxidation product of either trilinolein or arachidonic acid
Reference: 10004257-5
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A prominent autoxidation product of either trilinolein or arachidonic acid
Reference: 10004281-1
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A water soluble prodrug analog of AEA with similar activity to that of AEA in the growth inhibition of C6 glioma cells; also a structural variant of LPA, however, its effects on the various LPA receptors have not been...
Reference: 10004281-10
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A water soluble prodrug analog of AEA with similar activity to that of AEA in the growth inhibition of C6 glioma cells; also a structural variant of LPA, however, its effects on the various LPA receptors have not been...
Reference: 10004281-5
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A water soluble prodrug analog of AEA with similar activity to that of AEA in the growth inhibition of C6 glioma cells; also a structural variant of LPA, however, its effects on the various LPA receptors have not been...
Reference: 10004384-100
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A minor CYP450 metabolite of arachidonic acid that potently inhibits proximal tubule ATPase activity
Reference: 10004384-25
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A minor CYP450 metabolite of arachidonic acid that potently inhibits proximal tubule ATPase activity
Reference: 10004384-50
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A minor CYP450 metabolite of arachidonic acid that potently inhibits proximal tubule ATPase activity
Reference: 10004385-100
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A minor CYP450 metabolite of arachidonic acid that stimulates vasodilation of rabbit kidney
Reference: 10004385-25
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A minor CYP450 metabolite of arachidonic acid that stimulates vasodilation of rabbit kidney
Reference: 10004385-50
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A minor CYP450 metabolite of arachidonic acid that stimulates vasodilation of rabbit kidney
Reference: 10004413-1
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Immediate precursor of 4-HNE formed from ω-6 hydroperoxides such as linoleic acid and arachidonic acid
Reference: 10004413-10
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Immediate precursor of 4-HNE formed from ω-6 hydroperoxides such as linoleic acid and arachidonic acid
Reference: 10004413-5
€0.00 (tax incl.)
Immediate precursor of 4-HNE formed from ω-6 hydroperoxides such as linoleic acid and arachidonic acid
Reference: 10004413-500
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Immediate precursor of 4-HNE formed from ω-6 hydroperoxides such as linoleic acid and arachidonic acid
Reference: 10004946-100
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A structural analog of 14(15)-EET that antagonizes EET-induced relaxation of vascular smooth muscle
Reference: 10004946-25
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A structural analog of 14(15)-EET that antagonizes EET-induced relaxation of vascular smooth muscle
Reference: 10004946-50
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A structural analog of 14(15)-EET that antagonizes EET-induced relaxation of vascular smooth muscle
Reference: 10004946-500
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A structural analog of 14(15)-EET that antagonizes EET-induced relaxation of vascular smooth muscle
Reference: 10004970-1
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A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
Reference: 10004970-10
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A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
Reference: 10004970-25
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
Reference: 10004970-5
€0.00 (tax incl.)
A minor impurity produced in the synthesis of (+)-cloprostenol; 20-fold less active than (+)-cloprostenol in terminating pregnancy in the hamster
Reference: 10005000-1
€0.00 (tax incl.)
An ester of the free acid that is less water soluble, but more ,amenable for the formulation of stearidonate-containing diets and dietary supplements
Reference: 10005000-10
€0.00 (tax incl.)
An ester of the free acid that is less water soluble, but more ,amenable for the formulation of stearidonate-containing diets and dietary supplements
Reference: 10005000-5
€0.00 (tax incl.)
An ester of the free acid that is less water soluble, but more ,amenable for the formulation of stearidonate-containing diets and dietary supplements
Reference: 10005000-500
€0.00 (tax incl.)
An ester of the free acid that is less water soluble, but more ,amenable for the formulation of stearidonate-containing diets and dietary supplements
Reference: 10005032-1
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A C-7 truncated analog of LXA4 that is equiactive as LXA2 in the inhibition of LTB4-induced neutrophil chemotaxis (IC50 = 5 nM)
Reference: 10005032-10
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A C-7 truncated analog of LXA4 that is equiactive as LXA2 in the inhibition of LTB4-induced neutrophil chemotaxis (IC50 = 5 nM)
Reference: 10005032-5
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A C-7 truncated analog of LXA4 that is equiactive as LXA2 in the inhibition of LTB4-induced neutrophil chemotaxis (IC50 = 5 nM)
Reference: 10005098-10
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AMC-AA is one of several fatty acid amides which can be used to measure FAAH activity. Exposure of AMC-AA to FAAH results in the release of the fluorescent aminomethyl coumarin that absorbs at 360 nm and emits at 465...
Reference: 10005098-25
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AMC-AA is one of several fatty acid amides which can be used to measure FAAH activity. Exposure of AMC-AA to FAAH results in the release of the fluorescent aminomethyl coumarin that absorbs at 360 nm and emits at 465...
Reference: 10005098-5
€0.00 (tax incl.)
AMC-AA is one of several fatty acid amides which can be used to measure FAAH activity. Exposure of AMC-AA to FAAH results in the release of the fluorescent aminomethyl coumarin that absorbs at 360 nm and emits at 465...
Reference: 10005098-50
€0.00 (tax incl.)
AMC-AA is one of several fatty acid amides which can be used to measure FAAH activity. Exposure of AMC-AA to FAAH results in the release of the fluorescent aminomethyl coumarin that absorbs at 360 nm and emits at 465...
Reference: 10005099-100
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The primary oxygenation product of DHA when exposed to aspirin-inhibited COX-2; serves as a precursor to resolvins and has intrinsic biological activity, such as the inhibition of TNF-α-induced IL-1β expression in...
Reference: 10005099-25
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The primary oxygenation product of DHA when exposed to aspirin-inhibited COX-2; serves as a precursor to resolvins and has intrinsic biological activity, such as the inhibition of TNF-α-induced IL-1β expression in...
Reference: 10005099-250
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The primary oxygenation product of DHA when exposed to aspirin-inhibited COX-2; serves as a precursor to resolvins and has intrinsic biological activity, such as the inhibition of TNF-α-induced IL-1β expression in...
Reference: 10005099-50
€0.00 (tax incl.)
The primary oxygenation product of DHA when exposed to aspirin-inhibited COX-2; serves as a precursor to resolvins and has intrinsic biological activity, such as the inhibition of TNF-α-induced IL-1β expression in...
Reference: 10005123-150
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A divinyl ether oxylipin; formed in plants via 13-lipoxygenase-mediated formation of 13(S)-HpOTrE followed by conversion to the divinyl ether by divinyl ether synthase
Reference: 10005139-100
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A linoleic acid-derived oxylipin; formed via a 13-HpODE intermediate that is produced by lipoxygenase-mediated metabolism of linoleic acid; has been found in corn and sunflower seedlings
Reference: 10005143-100
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An oxylipin with diverse biological activities; has been found in various plants; is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble epoxide hydrolase-independent manner; inhibits antigen-induced...
Reference: 10005146-2
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An ω-6 polyunsaturated fatty acid; has been found as a minor component of bovine milk fat and in partially hydrogenated vegetable oils; levels increase in rabbit meat following supplementation with heated sunflower...
Reference: 10005157-100
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A very long-chain polyunsaturated fatty acid; has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids; found at low levels in mouse brain and spleen and levels decrease in the brain...
Reference: 10005157-25
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A very long-chain polyunsaturated fatty acid; has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids; found at low levels in mouse brain and spleen and levels decrease in the brain...
Reference: 10005157-250
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A very long-chain polyunsaturated fatty acid; has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids; found at low levels in mouse brain and spleen and levels decrease in the brain...
Reference: 10005157-50
€0.00 (tax incl.)
A very long-chain polyunsaturated fatty acid; has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids; found at low levels in mouse brain and spleen and levels decrease in the brain...
Reference: 10005165-100
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A VLCPUFA; has been found in tunny, herring, cod-liver, pilot whale, sardine, and squalus-suclii-liver oils, and bovine retina; a component of triglycerides and cholesterol esters in mouse and rat testis; produced...
Reference: 10005165-25
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A VLCPUFA; has been found in tunny, herring, cod-liver, pilot whale, sardine, and squalus-suclii-liver oils, and bovine retina; a component of triglycerides and cholesterol esters in mouse and rat testis; produced...
Reference: 10005165-50
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A VLCPUFA; has been found in tunny, herring, cod-liver, pilot whale, sardine, and squalus-suclii-liver oils, and bovine retina; a component of triglycerides and cholesterol esters in mouse and rat testis; produced...
Reference: 10005188-100
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A fluorescent fatty acid analog that alters its fluorescent emission spectra and intensity on entry into binding proteins
Reference: 10005188-25
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A fluorescent fatty acid analog that alters its fluorescent emission spectra and intensity on entry into binding proteins
Reference: 10005188-50
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A fluorescent fatty acid analog that alters its fluorescent emission spectra and intensity on entry into binding proteins
Reference: 10005223-10
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A selective inhibitor of AEA uptake that is resistant to FAAH hydrolysis; is the structurally “reversed” isomer of AM404; blocks the uptake of tritiated AEA with an EC50 value of about 1.5 µM in mouse cortical neurons
Reference: 10005223-100
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A selective inhibitor of AEA uptake that is resistant to FAAH hydrolysis; is the structurally “reversed” isomer of AM404; blocks the uptake of tritiated AEA with an EC50 value of about 1.5 µM in mouse cortical neurons
Reference: 10005223-5
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A selective inhibitor of AEA uptake that is resistant to FAAH hydrolysis; is the structurally “reversed” isomer of AM404; blocks the uptake of tritiated AEA with an EC50 value of about 1.5 µM in mouse cortical neurons
Reference: 10005223-50
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A selective inhibitor of AEA uptake that is resistant to FAAH hydrolysis; is the structurally “reversed” isomer of AM404; blocks the uptake of tritiated AEA with an EC50 value of about 1.5 µM in mouse cortical neurons
Reference: 10005439-1
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A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of glaucoma.(8941,8322,8839,9311) Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good...
Reference: 10005439-10
€0.00 (tax incl.)
A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of glaucoma.(8941,8322,8839,9311) Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good...
Reference: 10005439-25
€0.00 (tax incl.)
A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of glaucoma.(8941,8322,8839,9311) Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good...
Reference: 10005439-5
€0.00 (tax incl.)
A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of glaucoma.(8941,8322,8839,9311) Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good...
Reference: 10005440-1
€0.00 (tax incl.)
A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of glaucoma.(8941,8322,8839,9311) Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good...
Reference: 10005440-10
€0.00 (tax incl.)
A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of glaucoma.(8941,8322,8839,9311) Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good...
Reference: 10005440-25
€0.00 (tax incl.)
A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of glaucoma.(8941,8322,8839,9311) Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good...
Reference: 10005440-5
€0.00 (tax incl.)
A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of glaucoma.(8941,8322,8839,9311) Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good...
Reference: 10005455-1
€0.00 (tax incl.)
An endocannabinoid analog that does not bind to CB1, CB2, or TRPV1; at 5 mg/kg antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model;...
Reference: 10005455-10
€0.00 (tax incl.)
An endocannabinoid analog that does not bind to CB1, CB2, or TRPV1; at 5 mg/kg antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model;...
Reference: 10005455-25
€0.00 (tax incl.)
An endocannabinoid analog that does not bind to CB1, CB2, or TRPV1; at 5 mg/kg antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model;...
Reference: 10005455-5
€0.00 (tax incl.)
An endocannabinoid analog that does not bind to CB1, CB2, or TRPV1; at 5 mg/kg antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model;...
Reference: 10005459-1
€0.00 (tax incl.)
A selective FAAH inhibitor (IC50 = 5.25 nM in rat brain homogenates) with potential analgesic and anxiolytic activity; does not inhibit acidic PEAase or bind to CB1 or CB2 receptors
Reference: 10005459-10
€0.00 (tax incl.)
A selective FAAH inhibitor (IC50 = 5.25 nM in rat brain homogenates) with potential analgesic and anxiolytic activity; does not inhibit acidic PEAase or bind to CB1 or CB2 receptors
Reference: 10005459-25
€0.00 (tax incl.)
A selective FAAH inhibitor (IC50 = 5.25 nM in rat brain homogenates) with potential analgesic and anxiolytic activity; does not inhibit acidic PEAase or bind to CB1 or CB2 receptors
Reference: 10005459-5
€0.00 (tax incl.)
A selective FAAH inhibitor (IC50 = 5.25 nM in rat brain homogenates) with potential analgesic and anxiolytic activity; does not inhibit acidic PEAase or bind to CB1 or CB2 receptors
Reference: 10005609-1
€0.00 (tax incl.)
A prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling that may activate TRPV1 and TRPV4
Reference: 10005609-10
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A prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling that may activate TRPV1 and TRPV4
Reference: 10005609-5
€0.00 (tax incl.)
A prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling that may activate TRPV1 and TRPV4
Reference: 10005609-500
€0.00 (tax incl.)
A prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling that may activate TRPV1 and TRPV4
Reference: 10005610-1
€0.00 (tax incl.)
A prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling; may activate TRPV1 and TRPV4
Reference: 10005610-10
€0.00 (tax incl.)
A prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling; may activate TRPV1 and TRPV4
Reference: 10005610-5
€0.00 (tax incl.)
A prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling; may activate TRPV1 and TRPV4
Reference: 10005611-1
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A fatty acyl amide of taurine discovered during MS lipidomic analysis of rat brain
Reference: 10005611-10
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A fatty acyl amide of taurine discovered during MS lipidomic analysis of rat brain
Reference: 10005611-5
€0.00 (tax incl.)
A fatty acyl amide of taurine discovered during MS lipidomic analysis of rat brain
Reference: 10005728-1
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DL-α-lipoic acid is a cyclic disulfide antioxidant that interconverts with its reduced dithiol form. It is an essential cofactor for decarboxylation reactions of the citric acid cycle, and acts as a general...
Reference: 10005728-10
€0.00 (tax incl.)
DL-α-lipoic acid is a cyclic disulfide antioxidant that interconverts with its reduced dithiol form. It is an essential cofactor for decarboxylation reactions of the citric acid cycle, and acts as a general...
Reference: 10005728-25
€0.00 (tax incl.)
DL-α-lipoic acid is a cyclic disulfide antioxidant that interconverts with its reduced dithiol form. It is an essential cofactor for decarboxylation reactions of the citric acid cycle, and acts as a general...

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