MQAE

目录号: GC30035纯度: >99.50%同义词: 解毒喹
MQAE是一种非比例氯离子(Cl)猝灭荧光传感物,最大激发光/发射光波长为350/460nm,用于测量细胞内Cl浓度([Cl]i)。

MQAE
Cas No.: 162558-52-3
规格价格库存数量操作
50mg¥350.00现货
1
100mg¥560.00现货
1
200mg¥910.00现货
1
500mg¥1,960.00现货
1

文献被引

本产品暂无引用记录;以下为 GlpBio 产品在 Nature / Cell / Science 等顶刊的客户引用样例
  • Nature cover
    Nature
    641, 529–536 (2025)
  • Nature cover
    Nature
    628, 630–638 (2024)
  • Nature cover
    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
  • Science cover
    Science
    387(6739) (2025)
  • Science cover
    Science
    387(6734) (2025)
  • Cell Research cover
    Cell Research
    35, 97–116 (2025)
  • Cell Research cover
    Cell Research
    34, 683–706 (2024)
  • Cell Research cover
    Cell Research
    33, 273–287 (2023)
  • Cell Research cover
    Cell Research
    33, 546–561 (2023)
  • Cell Research cover
    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

产品描述 Description

MQAE functions as a non-ratiometric chloride ion (Cl) quenching fluorescent sensor that is employed to measure intracellular Cl concentration ([Cl]i), with the maximum wavelength excitation/emission(350/460nm)[1]. MQAE is suitable for surface fluorescence microscopy, confocal microscopy, two-photon microscopy, flow cytometry and other biochemical analysis experiments[1-2].The fluorescence intensity diminishes when MQAE concentration decreases and increases when MQAE concentration increases regardless of any changes in [Cl]i[2]. The intracellular distribution of MQAE is not uniform and is not affected by changes in cell volume caused by osmotic stress[3]. MQAE can bind to unknown subcellular structures, and these bound MQAE appear to enable the measurement of [Cl]i in airway-ciliated cells even in the presence of changes in cell volume[1,4]. MQAE can be used to create a fluorescent probe for the detection of mitochondrial chloride ions[5]. The fluorescence of MQAE-based probe is pH-insensitive in the physiological pH range and is quenched by chloride ions, with a Stern-Volmer quenching constant of 201M-1 at pH 7.0[5].

References:
[1] Ikeuchi Y, Kogiso H, Hosogi S, et al. Measurement of [Cl]i unaffected by the cell volume change using MQAE-based two-photon microscopy in airway ciliary cells of mice[J]. The journal of physiological sciences, 2018, 68: 191-199.
[2] Andersson C, Roomans G M. Determination of chloride efflux by X‐ray microanalysis versus MQAE‐fluorescence[J]. Microscopy research and technique, 2002, 59(6): 531-535.
[3] Koncz C, Daugirdas J T. Use of MQAE for measurement of intracellular [Cl] in cultured aortic smooth muscle cells[J]. American Journal of Physiology-Heart and Circulatory Physiology, 1994, 267(6): H2114-H2123.
[4] Miyazaki H, Shiozaki A, Niisato N, et al. Physiological significance of hypotonicity-induced regulatory volume decrease: reduction in intracellular Cl concentration acting as an intracellular signaling[J]. American Journal of Physiology-Renal Physiology, 2007, 292(5): F1411-F1417.
[5] Park S H, Shin I, Kim Y H, et al. Mitochondrial Cl-selective fluorescent probe for biological applications[J]. Analytical Chemistry, 2020, 92(18): 12116-12119.

MQAE是一种非比例氯离子(Cl)猝灭荧光传感物,最大激发光/发射光波长为350/460nm,用于测量细胞内Cl浓度([Cl]i[1]。MQAE适用于表面荧光显微镜、共聚焦显微镜、双光子显微镜以及流式细胞术等生化分析实验[1-2]。无论[Cl]i变化如何,当MQAE浓度降低时,荧光强度减弱;当MQAE浓度增加时,荧光强度增强[2]。MQAE在细胞内的分布不均匀,不受渗透压引起的细胞体积变化的影响[3]。MQAE可与未知的亚细胞结构结合,而且这些结合的MQAE似乎可以在细胞体积发生变化的情况下测定气道纤毛细胞中的[Cl]i [1,4]。MQAE可用于构建检测线粒体氯离子的荧光探针[5]。基于MQAE构建的探针的荧光在生理pH范围内对pH不敏感,被氯离子猝灭,在pH 7.0时Stern-Volmer猝灭常数为201M-1[5]

实验参考方法 Experimental Reference Method

本方案仅提供指南,应根据您的具体需要进行修改。

1. 制备MQAE染色液:

在Krebs-hepes缓冲液(20mM HEPES, 128mM NaCl, 2.5mM KCl, 2.7mM CaCl2, 1mM MgCl2, 16mM葡萄糖;pH 7.4)中制备成5-10mM的MQAE工作溶液。配置完成后,使用0.22μm过滤膜进行过滤灭菌。请根据实际情况调整MQAE工作液的浓度,现配现用。

2. 悬浮细胞染色(6 孔板方案)

(1)对于悬浮细胞:

将细胞悬液在1000×g离心3-5min,仔细抽吸上清。用Krebs-Hepes缓冲液洗涤细胞两次(每次洗涤5min),洗涤之间在1000×g离心。

(2)对于贴壁细胞:

用Krebs-hepes缓冲液冲洗贴壁细胞两次。胰蛋白酶分离细胞,然后在1000×g离心3-5min。

(3)染料培养:

将细胞颗粒重悬于1mL染色工作液中。室温下黑暗孵育30-60min(最佳孵育时间可能因细胞类型而异)。

(4)孵育后处理:

在1000×g下离心5min,仔细取出上清。用PBS洗涤细胞2-3次(每次洗涤5min),洗涤之间离心。

(5)复苏观察:

将染色细胞重悬于无血清培养基或PBS中。进行显微镜检查。

3. 贴壁细胞染色:

(1)细胞培养制备:

在无菌盖上培养贴壁细胞,直到达到所需的融合度。

(2)染色前处理:

小心地取出培养基,将盖子放在加湿的容器中。

(3)染料培养:

将100μL染色工作液涂抹在盖盖的一侧,轻轻倾斜,使细胞单层均匀覆盖。室温黑暗孵育30-60min。

(4)染色后洗涤:

抽吸染料溶液,用PBS冲洗盖子2-3次(每次冲洗5min)。

4. 显微镜分析:

用荧光显微镜或流式细胞术检测染色细胞。MQAE在350/460nm处表现出最大的激发/发射波长。

References:

[1] Koncz C, Daugirdas J T. Use of MQAE for measurement of intracellular [Cl?] in cultured aortic smooth muscle cells[J]. American Journal of Physiology-Heart and Circulatory Physiology, 1994, 267(6): H2114-H2123.

[2] Miyazaki H, Shiozaki A, Niisato N, et al. Physiological significance of hypotonicity-induced regulatory volume decrease: reduction in intracellular Cl? concentration acting as an intracellular signaling[J]. American Journal of Physiology-Renal Physiology, 2007, 292(5): F1411-F1417.

产品文档 Product Documents

Purity:>99.50%

化学性质Chemical Properties

CAS 号
162558-52-3
同义词
解毒喹
SMILES
COC1=CC2=CC=C[N+](CC(OCC)=O)=C2C=C1.[Br-]
分子式
C14H16BrNO3
分子量
326.19 g/mol
溶解性
DMSO : ≥ 35 mg/mL (107.30 mM)
保存条件
Store at -20°C, protect from light
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol