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Merck

C2624

Sigma-Aldrich

碳酸酐酶 来源于牛红细胞

≥95% (SDS-PAGE), specific activity ≥3,500 W-A units/mg protein, lyophilized powder

别名:

碳酸酐酶 来源于牛红细胞, 碳酸盐脱水酶, 碳酸酯水解酶

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About This Item

CAS号:
EC號碼:
MDL號碼:
分類程式碼代碼:
12352204
NACRES:
NA.54

生物源

bovine erythrocytes

品質等級

化驗

≥75% protein basis (biuret)
≥95% (SDS-PAGE)

形狀

lyophilized powder

比活性

≥3,500 W-A units/mg protein

溶解度

deionized water: >10 mg/mL

儲存溫度

2-8°C

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應用

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

單位定義

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)。

象形圖

Health hazard

訊號詞

Danger

危險聲明

防範說明

危險分類

Resp. Sens. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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
Joana da Costa Ores et al.
Chemosphere, 88(2), 255-259 (2012-04-20)
This work presents a study of industrially applicable techniques to obtain a biologically supported carbon dioxide capture system, based on the extraction of carbonic anhydrase from bovine blood. Carbonic anhydrase is a metalloenzyme which catalyzes the reversible hydration of carbon
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
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
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

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