Literature DB >> 10603235

A luminescent ruthenium complex for ultrasensitive detection of proteins immobilized on membrane supports.

K Berggren1, T H Steinberg, W M Lauber, J A Carroll, M F Lopez, E Chernokalskaya, L Zieske, Z Diwu, R P Haugland, W F Patton.   

Abstract

SYPRO Ruby protein blot stain provides a sensitive, gentle, fluorescence-based method for detecting proteins on nitrocellulose or polyvinylidene difluoride (PVDF) membranes. SYPRO Ruby dye is a permanent stain composed of ruthenium as part of an organic complex that interacts noncovalently with proteins. Stained proteins can be excited by ultraviolet light of about 302 nm or with visible light of about 470 nm. Fluorescence emission of the dye is approximately 618 nm. The stain can be visualized using a wide range of excitation sources utilized in image analysis systems including a UV-B transilluminator, 488-nm argon-ion laser, 532-nm yttrium-aluminum-garnet (YAG) laser, blue fluorescent light bulb, or blue light-emitting diode (LED). The detection sensitivity of SYPRO Ruby protein blot stain (0.25-1 ng protein/mm(2)) is superior to that of amido black, Coomassie blue, and india ink staining and nearly matches colloidal gold staining. SYPRO Ruby protein blot stain visualizes proteins more rapidly than colloidal gold stain and the linear dynamic range is more extensive. Unlike colloidal gold stain, SYPRO Ruby protein blot stain is fully compatible with subsequent biochemical applications including colorimetric and chemiluminescent immunoblotting, Edman-based sequencing and mass spectrometry. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10603235     DOI: 10.1006/abio.1999.4364

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  13 in total

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Journal:  J Chem Biol       Date:  2010-06-19

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Authors:  Karla J Daniels; Yang-Nim Park; Thyagarajan Srikantha; Claude Pujol; David R Soll
Journal:  Eukaryot Cell       Date:  2013-08-16

5.  Phosphoprotein stability in clinical tissue and its relevance for reverse phase protein microarray technology.

Authors:  Virginia Espina; Claudius Mueller; Lance A Liotta
Journal:  Methods Mol Biol       Date:  2011

6.  Detection of Proteins on Blot Membranes.

Authors:  Aaron Goldman; Sandra Harper; David W Speicher
Journal:  Curr Protoc Protein Sci       Date:  2016-11-01

7.  Use of the REVERT® total protein stain as a loading control demonstrates significant benefits over the use of housekeeping proteins when analyzing brain homogenates by Western blot: An analysis of samples representing different gonadal hormone states.

Authors:  Z Z Kirshner; R B Gibbs
Journal:  Mol Cell Endocrinol       Date:  2018-02-01       Impact factor: 4.102

8.  Coomassie blue as a near-infrared fluorescent stain: a systematic comparison with Sypro Ruby for in-gel protein detection.

Authors:  R Hussain Butt; Jens R Coorssen
Journal:  Mol Cell Proteomics       Date:  2013-09-16       Impact factor: 5.911

9.  Highlights on the capacities of "Gel-based" proteomics.

Authors:  François Chevalier
Journal:  Proteome Sci       Date:  2010-04-28       Impact factor: 2.480

10.  Reverse-Phase Protein Array: Technology, Application, Data Processing, and Integration.

Authors:  Cristian Coarfa; Sandra L Grimm; Kimal Rajapakshe; Dimuthu Perera; Hsin-Yi Lu; Xuan Wang; Kurt R Christensen; Qianxing Mo; Dean P Edwards; Shixia Huang
Journal:  J Biomol Tech       Date:  2021-04
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