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Merck

C0733

Sigma-Aldrich

环氧化酶 1 来源于绵羊

glycerol solution, ≥1500 units/mg protein

别名:

COX-1, Constitutive cyclooxygenase, Prostaglandin H synthase 1, Prostaglandin endoperoxide synthase

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About This Item

MDL號碼:
分類程式碼代碼:
12352204
NACRES:
NA.32

形狀

glycerol solution

品質等級

比活性

≥1500 units/mg protein

分子量

dimer subunit mol wt 70 kDa

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−70°C

基因資訊

sheep ... COX1(808251)

一般說明

环氧合酶 1 是一种分子量为 71 kDa 的膜结合蛋白,主要存在于内质网中。它有三个结构域,即表皮生长因子(EGF)样域、酶结构域和膜结合域。环氧合酶 1 介导前列腺素合成,并受抗炎非甾体药物调节。

應用

在骨关节炎样品的蛋白免疫印迹分析 和前列腺素合成酶活性测定中,来自绵羊的环氧合酶 1 已用作阳性对照蛋白。

生化/生理作用

COX-1 催化花生四烯酸转化为前列腺素 H 2 (前列腺素、血栓素和前列环素生物合成的第一步)。它参与类花生酸的稳态角色,并在几乎所有动物组织中组成性表达。其中,花生四烯酸的表观 K M 为 8.3μM 。

單位定義

在37°C下,一个单位在含 100μM花生四烯酸盐、5 mM EDTA、2 mM 苯酚和 1 μM血色素的 0.1 MTris-HCl 缓冲液 (pH 8) 中每分钟消耗 1 纳摩尔氧气。

外觀

溶液溶于 80 mM Tris-HCl,pH 8,含 0.1% 吐温 ® 20,300μM 二乙基二硫代氨基甲酸酯和 10% 甘油。

法律資訊

TWEEN is a registered trademark of Croda International PLC

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Sze Chern Lim et al.
American journal of human genetics, 94(2), 209-222 (2014-01-28)
Leigh syndrome (LS) is a severe neurodegenerative disorder with characteristic bilateral lesions, typically in the brainstem and basal ganglia. It usually presents in infancy and is genetically heterogeneous, but most individuals with mitochondrial complex IV (or cytochrome c oxidase) deficiency
Michela Zago et al.
Toxicology letters, 226(2), 107-116 (2014-01-30)
Diseases due to cigarette smoke exposure, including chronic obstructive pulmonary disease (COPD) and lung cancer, are associated with chronic inflammation typified by the increased expression of cyclooxygenase-2 (COX-2) protein. RelB is an NF-κB family member that suppresses cigarette smoke induction
Maurizio Anzini et al.
Journal of medicinal chemistry, 56(8), 3191-3206 (2013-03-29)
A series of 3-substituted 1,5-diarylpyrroles bearing a nitrooxyalkyl side chain linked to different spacers were designed. New classes of pyrrole-derived nitrooxyalkyl inverse esters, carbonates, and ethers (7-10) as COX-2 selective inhibitors and NO donors were synthesized and are herein reported.
Cyclo-oxygenase isoenzymes: physiological and pharmacological role
Kam PCA and See AUL
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LaCourse EJ, et al.
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