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Merck
CN

SRE0045

Sigma-Aldrich

荧光素酶 来源于北美萤火虫 (萤火虫)

recombinant, expressed in E. coli, lyophilized powder, ≥10×1010 units/mg protein

别名:

荧光素酶

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About This Item

CAS号:
MDL编号:
UNSPSC代码:
12352204
NACRES:
NA.54

重组

expressed in E. coli

质量水平

形式

lyophilized powder

比活

≥10×1010 units/mg protein

分子量

62 kDa

应用

diagnostic assay manufacturing

储存温度

−20°C

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相关类别

应用

萤火虫荧光素酶在分子和细胞生物学中广泛使用,特别是用于 ATP 的有效检测和定量,并作为遗传功能的报告基因。

生化/生理作用

萤火虫荧光素酶是一种 62 kDa 的蛋白质,催化光的产生。这种酶需要 ATP、分子氧和杂环化合物萤火虫荧光素,在两步过程中产生光。光产生反应由荧光素活化(其羧基的腺苷酸化)启动,并在分子氧存在下进行,产生黄绿色光光子。

单位定义

一个荧光素酶单位在 20-25℃ 下将在10 秒内产生一个相对光单位 (RLU),使用 GloMax 20/20 光度计在Tris-甘氨酸缓冲液中含有40pmol ATP和15nmol荧光素的100μl测定混合物中测定,溶液PH值为7.6。

单位定义换算系数:每个传统照明单位大约有 9000 个相对照明单位 (RLU),在PPO / POPOP混合物中使用相当于0.02μ Ci 14 C 的峰高。

外形

以含有 HEPES (pH 7.5)、NaCl、MgCl 2 、EDTA、DTT 的冻干粉和碳水化合物稳定剂形式提供。
本品是由 大肠杆菌表达的 luc 基因产生的来自 Photinus pyralis(美国萤火虫)的重组荧光素酶 (62 kDa)

制备说明

为了获得最大溶解度,重要的是在高盐浓度下复溶酶,如 1 MTris 缓冲液与 pH 7-8 的任何反离子。制备的酶浓度每毫升可高达 5 mg 蛋白。切勿涡旋,避免搅拌。
复溶后,酶溶液可在 4-8°C 下保存长达 2 天,或在-20°C 下以工作等份冷冻保存至少一个月。不推荐反复冻融。

象形图

Health hazardCorrosion

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - Resp. Sens. 1

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品

分析证书(COA)

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Julia Adelöf et al.
Aging cell, 20(4), e13336-e13336 (2021-03-16)
With age, protein damage accumulates and increases the risk of age-related diseases. The proteasome activator PA28αβ is involved in protein damage clearance during early embryogenesis and has demonstrated protective effects against proteinopathy. We have recently discovered that adult female mice
Maura Greiser et al.
eLife, 12 (2023-06-05)
Mitochondrial ATP production in ventricular cardiomyocytes must be continually adjusted to rapidly replenish the ATP consumed by the working heart. Two systems are known to be critical in this regulation: mitochondrial matrix Ca2+ ([Ca2+]m) and blood flow that is tuned
Aleksey Yevtodiyenko et al.
Nature communications, 12(1), 2680-2680 (2021-05-13)
Bioluminescent imaging (BLI) is one of the most powerful and widely used preclinical imaging modalities. However, the current technology relies on the use of transgenic luciferase-expressing cells and animals and therefore can only be applied to a limited number of
S R Ford et al.
Journal of bioluminescence and chemiluminescence, 7(3), 185-193 (1992-07-01)
Commercially available crystalline native and recombinant firefly luciferases were compared. The two types of luciferase had indistinguishable responses to variation in ATP and luciferin concentrations and to omission of reaction components. The time courses of light production, the responses to
Pratik Vyas et al.
Journal of the American Chemical Society, 145(15), 8344-8354 (2023-03-24)
Reactions involving the transfer of a phosphoryl (-PO32-) group are fundamental to cellular metabolism. These reactions are catalyzed by enzymes, often large and complex, belonging to the phosphate-binding loop (P-loop) nucleoside triphosphatase (NTPase) superfamily. Due to their critical importance in

商品

Firefly luciferase is a sensitive reporter for gene studies due to its absence in mammalian cells or tissues.

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