Merck
CN

B6529

Sigma-Aldrich

亮蓝R染色液

ethanol solution

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别名:
酸性蓝83, Coomassie 亮蓝R, 亮吲哚蓝蛋白 6B, 酸性蓝 83
经验公式(希尔记法):
C45H44N3NaO7S2
CAS号:
分子量:
825.97
颜色索引号:
42660
Beilstein:
5718025
MDL编号:
PubChem化学物质编号:
NACRES:
NA.47

形式

ethanol solution

质量水平

application(s)

diagnostic assay manufacturing
hematology
histology

储存温度

room temp

SMILES string

[Na+].CCOc1ccc(Nc2ccc(cc2)C(\c3ccc(cc3)N(CC)Cc4cccc(c4)S([O-])(=O)=O)=C5\C=C/C(C=C5)=[N+](\CC)Cc6cccc(c6)S([O-])(=O)=O)cc1

InChI

1S/C45H45N3O7S2.Na/c1-4-47(31-33-9-7-11-43(29-33)56(49,50)51)40-23-15-36(16-24-40)45(35-13-19-38(20-14-35)46-39-21-27-42(28-22-39)55-6-3)37-17-25-41(26-18-37)48(5-2)32-34-10-8-12-44(30-34)57(52,53)54;/h7-30H,4-6,31-32H2,1-3H3,(H2,49,50,51,52,53,54);/q;+1/p-1

InChI key

NKLPQNGYXWVELD-UHFFFAOYSA-M

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应用

亮蓝R染色溶液专门设计用于在免疫电泳和Ouchterlony凝胶之后对琼脂糖凝胶中的蛋白质进行染色。污渍含有乙醇和乙酸,因此在染色前无需固定凝胶。首先用水和盐水洗涤免疫电泳或Ouchterlony凝胶,以去除未沉淀的蛋白质,然后干燥。然后将凝胶浸入染色溶液中30分钟,并用10%乙酸脱色。
电泳后检测蛋白条带。

组分

0.5% (w/v) 亮蓝 R、45% (v/v) 乙醇和 10% (v/v) 乙酸。

分析说明

在免疫电泳后测试琼脂糖凝胶的适用性。

法律信息

象形图

FlameExclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

81.0 °F - closed cup

闪点(°C)

27.2 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品

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Wei Zhang et al.
International journal of oncology, 54(5), 1719-1733 (2019-03-14)
Ovarian cancer remains the most lethal type of cancer among all gynecological malignancies. The majority of patients are diagnosed with ovarian cancer at the late stages of the disease. Therefore, there exists an imperative need for the development of early
Jerome C Servaites et al.
Analytical biochemistry, 421(1), 75-80 (2011-12-06)
Protein is a large component of the standing biomass of algae. The total protein content of algae is difficult to measure because of the problems encountered in extracting all of the protein from the cells. Here we modified an existing
E Zeindl-Eberhart et al.
Electrophoresis, 18(5), 799-801 (1997-05-01)
A new, easy method for the immunodetection of specific antigens in two-dimensional electrophoresis (2-DE) is described. Areas of 2-DE gels containing antigens of interest are electrophoretically transferred to polyvinylidene difluoride membranes, immunostained with specific antibodies using Fast Red or 5-bromo-4-chloro-3-indolyl
Zhang Xin-Guo Chen Jian-Hua et al.
Journal of chromatographic science, 50(9), 820-825 (2012-06-22)
A human serum albumin and Thymosin α1 (HSA-Tα1) fusion protein was designed and over-expressed in Pichia pastoris. To purify the fusion protein, a new native preparative electrophoresis system that involved a modified device with a sample receiving chamber, and an
Reiner Westermeier
Proteomics, 6 Suppl 2, 61-64 (2006-10-13)
In spite of the high sensitivity of silver staining and the wide dynamic range of various fluorescent detection methods, Coomassie Brilliant Blue staining is still the most widely used protein detection technique for proteins separated by polyacrylamide gel electrophoresis. There

商品

To meet the great diversity of protein analysis needs, Sigma offers a wide selection of protein visualization (staining) reagents. EZBlue™ and ProteoSilver™, designed specifically for proteomics, also perform impressively in traditional PAGE formats.

为满足蛋白分析的多样化需求,Sigma提供多种蛋白质可视化(染色)试剂。EZBlue™和ProteoSilver™专为蛋白质组学而设计,即使在传统的PAGE形式中依然表现出色。

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