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Colloidal coomassie stain

一种考马斯亮蓝、体制剂的技术,应用在仪器、分析材料、生物材料分析等方向,能够解决性能不可接受等问题

Active Publication Date: 2015-12-02
BIO RAD LAB INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Simply substituting ethanol for methanol would render the formulation unacceptable

Method used

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  • Colloidal coomassie stain
  • Colloidal coomassie stain
  • Colloidal coomassie stain

Examples

Experimental program
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Embodiment

[0033] A series of formulations were created to prepare safer and more stable stains than existing methanolic 2-part protein stains. An exemplary standard 2-part stain formulation comprising 8% ammonium sulfate, 1.6% orthophosphoric acid, 0.08% Coomassie Brilliant Blue G-250, and 20% methanol was made up in deionized water. Initial simplistic attempts to replace methanol with ethanol failed, resulting in formulations with significant sedimentation.

[0034] Afterwards, the surfactant Pluronic F-127 was added to the Coomassie Brilliant Blue G-250 formulation containing 7.8% ammonium sulfate, 2.2% orthophosphoric acid, and 14.2% ethanol. The formulations were formulated with different levels of Pluronic F-127 and the stains were stored in covered vessels for 5 days. Decant the removed material and observe the remaining precipitate. Concentrations as low as 0.05% Pluronic F-127 prevented precipitate formation. In addition, the effect of surfactant concentration on relative pro...

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PUM

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Abstract

Colloidal formulation for staining proteins and methods of their use are provided.

Description

[0001] Cross References to Related Applications [0002] This application claims priority to US Provisional Patent Application Serial No. 61 / 777,801, filed March 12, 2013, which is incorporated herein by reference. Background of the invention [0003] Electrophoresis gels can be stained to a defined endpoint with Coomassie Brilliant Blue G-250, since the dye can be prepared in colloidal form, which does not enter the gel to be stained, but is absorbed by the protein bands in the gel, Allow sufficient time to diffuse throughout the strip to saturate the strip. Because the colloidal form does not enter the gel itself, the background is very low, thereby reducing the need for a destaining step that can result in a decrease in the intensity of the stained protein bands. [0004] Electrophoresis gels are usually stained with two-part stains. The 2-part stain needs to be prepared fresh before each use to have the desired properties (eg, low background). 2-Part stains quickly form...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N1/30G01N33/68
CPCG01N33/6839G01N33/68Y10T436/10Y10T436/107497
Inventor C·贝利斯勒L·奥列奇T·伯克曼G·普拉维那
Owner BIO RAD LAB INC
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