推荐产品
应用
来自牛红细胞的碳酸酐酶用于创建二氧化碳捕获系统和研究各种纯化技术 。碳酸酐酶也用于研究鱼类的酸碱调节和碳酸酐酶 II 类型缺乏综合征 。
生化/生理作用
碳酸酐酶是一种含锌的酶，催化二氧化碳可逆地转化为碳酸氢盐。它的主要生理作用之一是维持血液和其他组织中的酸碱平衡。碳酸酐酶缺乏导致碳酸酐酶 II 类型缺乏综合征，是一种常染色体隐性遗传疾病，可引起骨硬化症、肾小管酸中毒和脑钙化 。
单位定义
一个 Wilbur-Anderson (W-A) 单位将导致 0.02 MTrizma 缓冲液的 pH 值在 0°C 下从 8.3 降至 6.3/min（一个 W-A 单位基本上相当于一个 Roughton-Booth 单位）。
警示用语：
Danger
危险声明
预防措施声明
危险分类
Resp. Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
动植物源性产品
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
Nicolas Ghéczy et al.
RSC advances, 10(32), 18655-18676 (2020-05-18)
Enzyme-catalysed cascade reactions in flow-through systems with immobilised enzymes currently are of great interest for exploring their potential for biosynthetic and bioanalytical applications. Basic studies in this field often aim at understanding the stability of the immobilised enzymes and their
Abdur Rauf et al.
Chemistry & biodiversity, 14(6) (2017-02-17)
Plant phenolics are known to display many pharmacological activities. In the current study, eight phenolic compounds, e.g., luteolin 5-O-β-glucoside (1), methyl rosmarinate (2), apigenin (3), vicenin 2 (4), lithospermic acid (5), soyasaponin II (6), rubiadin 3-O-β-primeveroside (7), and 4-(β-d-glucopyranosyloxy)benzyl 3,4-dihydroxybenzoate
K M Gilmour et al.
The Journal of experimental biology, 212(Pt 11), 1647-1661 (2009-05-19)
Carbonic anhydrase (CA) is the zinc metalloenzyme that catalyses the reversible reactions of CO(2) with water. CA plays a crucial role in systemic acid-base regulation in fish by providing acid-base equivalents for exchange with the environment. Unlike air-breathing vertebrates, which
Marco Catalano et al.
Analytical chemistry, 92(15), 10822-10829 (2020-07-04)
The availability of reliable methods for the characterization of the binding of small molecule ligands to protein targets is crucially important for drug discovery. We have adapted a method, routinely used for the characterization of monoclonal antibodies (enzyme-linked immunosorbent assay
Thomas M Bosley et al.
Brain : a journal of neurology, 134(Pt 12), 3502-3515 (2011-11-29)
Carbonic anhydrase type II deficiency syndrome is an uncommon autosomal recessive disease with cardinal features including osteopetrosis, renal tubular acidosis and brain calcifications. We describe the neurological, neuro-ophthalmological and neuroradiological features of 23 individuals (10 males, 13 females; ages at
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门