021-51111890
购物车（）
sales@molnova.cn
N-Dodecyl-β-D-maltoside
CAS No. 69227-93-6
N-Dodecyl-β-D-maltoside ( Lauryl Maltoside )
产品货号. M23114 CAS No. 69227-93-6
N-十二烷基-β-D-麦芽糖苷（月桂基麦芽糖苷）是芘 (Py) 的衍生物，是一种烷基麦芽糖苷清洁剂，特别是在转运蛋白和呼吸复合物中。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 10MG | ￥129 | 有现货 |
|
| 25MG | ￥184 | 有现货 |
|
| 50MG | ￥269 | 有现货 |
|
| 100MG | ￥372 | 有现货 |
|
| 500MG | ￥745 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称N-Dodecyl-β-D-maltoside
-
注意事项本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断
-
产品简述N-十二烷基-β-D-麦芽糖苷（月桂基麦芽糖苷）是芘 (Py) 的衍生物，是一种烷基麦芽糖苷清洁剂，特别是在转运蛋白和呼吸复合物中。
-
产品描述N-Dodecyl-β-D-maltoside (Lauryl Maltoside) is a derivatives of pyrene (Py), and it is a alkyl maltopyranoside detergent, especially in transporters and respiratory complexes. N-Dodecyl-β-D-maltoside has also been employed in applications such as in the purification and stabilization of RNA polymerase and detection of protein-lipid interactions.
-
体外实验——
-
体内实验——
-
同义词Lauryl Maltoside
-
通路Others
-
靶点Other Targets
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number69227-93-6
-
分子量510.62
-
分子式C??H??O??
-
纯度>98% (HPLC)
-
溶解度H2O : 100 mg/mL (195.84 mM; Need ultrasonic)
-
SMILES——
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Zahid NI, et al. Evidence of Increased Hydrophobicity and Dynamics inside the Tail Region of Glycolipid Self-Assemblies Using 2-n-Alkyl-Pyrene Derivatives to Probe Different Locations. Langmuir. 2019 Jul 23;35(29):9584-9592.
产品手册
关联产品
-
Suriclone
Suriclone (RP 31264) is a selective cyclic pyrrolidone analog with sedative and anxiolytic activity, but not significant sedative effects.Suriclone shows its effects by modulating GABA-A receptors.
-
Amino-PEG14-alcohol
Amino-PEG14-alcohol 是一种基于 PEG 的 PROTAC 连接体，可用于 PROTAC 的合成。
-
cGMP Dependent Kinas...
Competitive inhibitor of cGMP-dependent protein kinase (PKG); analog of a substrate peptide corresponding to a phosphorylation site of histone H2B. Competes with synthetic substrates (Ki = 86 mM) but does not inhibit phosphorylation of intact histones by PKG. Inhibits phosphorylation of intact histones by PKA.
