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MES sodium salt Sale

(Synonyms: 吗啉乙磺酸钠盐; 2-Morpholinoethanesulphonic acid sodium salt) 目录号 : GC61042

MES(2-Morpholinoethanesulphonicacid)sodiumsalt是一种两性离子缓冲液,在pH值5.5-7.7范围内有效。MESsodiumsalt作为一种Good's缓冲液,广泛应用于植物培养基、试剂溶液和生理实验中调节pH值。

MES sodium salt Chemical Structure

Cas No.:71119-23-8

规格 价格 库存 购买数量
500mg
¥495.00
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Sample solution is provided at 25 µL, 10mM.

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Quality Control & SDS

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产品描述

MES (2-Morpholinoethanesulphonic acid) sodium salt, a zwitterionic buffer, is effective in the pH range of 5.5-7.7. MES sodium salt, as one of the Good's buffers, is broadly used to regulate pH value for plants culture medium, reagent solution, and physiological experiments[1][2].

[1]. Kagenishi T, et al. MES Buffer Affects Arabidopsis Root Apex Zonation and Root Growth by Suppressing Superoxide Generation in Root Apex. Front Plant Sci. 2016;7:79. Published 2016 Feb 18. [2]. Mash HE, et al. Complexation of copper by zwitterionic aminosulfonic (good) buffers. Anal Chem. 2003;75(3):671-677.

Chemical Properties

Cas No. 71119-23-8 SDF
别名 吗啉乙磺酸钠盐; 2-Morpholinoethanesulphonic acid sodium salt
Canonical SMILES O=S(CCN1CCOCC1)(O[Na])=O
分子式 C6H12NNaO4S 分子量 217.22
溶解度 储存条件 Store at -20°C
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。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 4.6036 mL 23.0181 mL 46.0363 mL
5 mM 0.9207 mL 4.6036 mL 9.2073 mL
10 mM 0.4604 mL 2.3018 mL 4.6036 mL
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*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Glpbio的产品页面获得)批次特异的分子量使用本工具。

计算

动物体内配方计算器 (澄清溶液)

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
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
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Research Update

Staining for viability testing, germination and maturation of Sambucus nigra L. pollen in vitro

Biotech Histochem 2018;93(4):258-266.PMID:29611720DOI:10.1080/10520295.2018.1425912.

Freshly released pollen of black elderberry (Sambucus nigra L.) was incubated under various culture conditions until germination was achieved. Optimal conditions for germination were determined and used for maturation of unicellular microspores in vitro. Staining with 5-diphenyltetrazolium bromide, propidium iodide and iodine potassium iodide was used to assess pollen viability, nuclear phase and maturation, respectively. The germination rate was highest when fresh pollen was agitated at 40 rpm in Petri dishes containing a liquid medium consisting of Brewbaker and Kwack salts, 15% (w/v) sucrose, 500 mg/l MES sodium salt, at pH 5.0; germination reached nearly 70% after only 1 h in culture. Under these conditions, and with addition of 200 mg/l glutamine, 260 mg/l cytidine and 500 mg/l uridine, uninucleate microspores developed into mature pollen at a 12% germination rate. Our report is the first demonstration of maturation of S. nigra microspores in vitro.