KMG-301AM TFA
目录号 : GC72967KMG-301AM TFA是KMG-301的乙酰氧基甲酯化形式。
Cas No.:1372642-78-8
Sample solution is provided at 25 µL, 10mM.
KMG-301AM TFA is the acetoxy metl esterified form of KMG-301. KMG-301AM TFA successfully accumulates in mitochondria and then it is drolyzed to KMG-301. KMG-301 is an Mg2+-selective fluorescent probe functional in mitochondria in intact cells. Since the mitochondrial membrane is impermeable to KMG-301, it is not released upon depolarization of the mitochondrial membrane potential. KMG-301 can indicate changes in mitochondrial Mg2+ concentration and shows Mg2+ transport across the mitochondrial membrane in the early phases of a cellular model.
Experimental Protocols: This protocol only provides a guideline, and should be modified according to your specific needs[1]. 1. For optical imaging, 20 µM KMG-301AM TFA is applied to cells in Hanks' balanced salt solutions (HBSS) for 10 min on ice, so that drolysis of the acetoxymetl ester by esterase present in the cytosol will be avoided. HBSS contains (in mM): NaCl, 137; KCl, 5.4; CaCl2, 1.3; MgCl2, 0.5; MgSO4, 0.4; Na2HPO4, 0.3; KH2PO4, 0.4; NaHCO3, 4.2; D-glucose, 5.6; HEPES, 5 (pH adjusted to 7.4 with NaOH). 2. Then, the cells are washed twice with HBSS and incubated for 15 min at 37°C to allow for complete drolysis of the acetoxymetl ester form in mitochondria. 3. If you want the simultaneous use of KMG-104AM and KMG-301AM TFA, cells are incubated with 5 µM KMG-104AM in HBSS for 30 min at 37°C, and then stained with KMG-301AM TFA. 4. Isolated mitochondria are incubated with 20 µM KMG-301AM TFA in Mitochondria Imaging Buffer (MIB) for 20 min at 37°C. Then, mitochondria are washed twice with MIB and further incubated for 15 min at 37°C. MIB contains (in mM): KCl, 125; K2HPO4, 2; MgCl2, 1; HEPES, 5; EDTA, 0.02 (pH adjusted to 7.2 with KOH) or Mg2+-free MIB (without MgCl2)5. Fluorescence imaging experiments are performed using a confocal laser scanning microscope system. KMG-301 is excited at 559 nm from a laser diode, and the signal was observed at 600-700 nm. In the simultaneous measurement, KMG-104 and KMG-301 were excited at 488 nm from an Argon laser and 559 nm, respectively. Fluorescence was separated using a 560 nm dichroic mirror and observed at 500-545 nm and 600-700 nm, respectively.
References:
[1]. Shindo Y, et al. Newly developed Mg2+-selective fluorescent probe enables visualization of Mg2+ dynamics in mitochondria. PLoS One. 2011;6(8):e23684.
Cas No. | 1372642-78-8 | SDF | |
分子式 | C32H28F3N3O8 | 分子量 | 639.58 |
溶解度 | 储存条件 | -20°C, protect from light, stored under nitrogen | |
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℃,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。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 1.5635 mL | 7.8176 mL | 15.6353 mL |
5 mM | 0.3127 mL | 1.5635 mL | 3.1271 mL |
10 mM | 0.1564 mL | 0.7818 mL | 1.5635 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >95.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet