Coomassie Fluor™ Orange Protein Gel Stain (Ready-To-Use Solution)
Citas y referencias (8)
Invitrogen™
Coomassie Fluor™ Orange Protein Gel Stain (Ready-To-Use Solution)
La tinción de gel de proteína naranja Coomassie Fluor patentada por Molecular Probes proporciona una tinción rápida, sencilla y sensibleMás información
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Número de catálogo
Cantidad
C33250
1 L
Número de catálogo C33250
Precio (MXN)
-
Cantidad:
1 L
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La tinción de gel de proteína naranja Coomassie Fluor patentada por Molecular Probes proporciona una tinción rápida, sencilla y sensible de las proteínas separadas por SDS-PAGE. Después de la electroforesis, el gel se tiñe, se enjuaga y se fotografía. La tinción se completa en menos de una hora: no se requieren pasos de fijación o decoloración por separado y no hay riesgo de sobretinción del gel. Las proteínas teñidas se pueden visualizar mediante un transiluminador UV estándar de 300 nm o un escáner basado en láser. La tinción de gel de proteína naranja Coomassie Fluor también está disponible en un tamaño de 5 litros (Cat. nro. C-33251).
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Ubicación de detecciónDetección en gel
Método de detecciónFluorescente
Excitación/emisión300, 470/570 nm
Línea de productosCoomassie Fluor
Tipo de productoTinción para geles de proteínas
Cantidad1 L
Condiciones de envíoTemperatura ambiente
Molécula dianaproteína
Etiqueta o tinteCoomassie Fluor naranja
Unit SizeEach
Contenido y almacenamiento
Almacenar a temperatura ambiente y proteger de la luz.
Citations & References (8)
Citations & References
Abstract
Molecular mechanism of the inhibitory effect of cobalt ion on thermolysin activity and the suppressive effect of calcium ion on the cobalt ion-dependent inactivation of thermolysin.
Authors:Hashida Y, Inouye K,
Journal:J Biochem
PubMed ID:17405797
'Thermolysin activity in the hydrolysis of N-[3-(2-furyl)acryloyl]-glycyl-l-leucine amide (FAGLA) and FA-l-leucyl-l-alanine amide (FALAA) was examined at various Co(2+) and Ca(2+) concentrations. It decreased to 28% with increasing [Co(2+)] up to 18 mM. The Co(2+)-dependent inactivation was in part suppressed by adding Ca(2+) ion up to 0.5 mM, but 33% of ... More
Covalently dimerized SecA is functional in protein translocation.
Authors:de Keyzer J, van der Sluis EO, Spelbrink RE, Nijstad N, de Kruijff B, Nouwen N, van der Does C, Driessen AJ,
Journal:J Biol Chem
PubMed ID:16115882
'The ATPase SecA provides the driving force for the transport of secretory proteins across the cytoplasmic membrane of Escherichia coli. SecA exists as a dimer in solution, but the exact oligomeric state of SecA during membrane binding and preprotein translocation is a topic of debate. To study the requirements of ... More
Recombinant human immunodeficiency virus type 1 integrase exhibits a capacity for full-site integration in vitro that is comparable to that of purified preintegration complexes from virus-infected cells.
Authors:Sinha S, Grandgenett DP,
Journal:J Virol
PubMed ID:15956566
Retrovirus preintegration complexes (PIC) in virus-infected cells contain the linear viral DNA genome (approximately 10 kbp), viral proteins including integrase (IN), and cellular proteins. After transport of the PIC into the nucleus, IN catalyzes the concerted insertion of the two viral DNA ends into the host chromosome. This successful insertion ... More
Genetic determinants of Silicibacter sp. TM1040 motility.
Authors:Belas R, Horikawa E, Aizawa S, Suvanasuthi R,
Journal:J Bacteriol
PubMed ID:19482930
Silicibacter sp. TM1040 is a member of the marine Roseobacter clade of Alphaproteobacteria that forms symbioses with unicellular eukaryotic phytoplankton, such as dinoflagellates. The symbiosis is complex and involves a series of steps that physiologically change highly motile bacteria into cells that readily form biofilms on the surface of the ... More
Role for leptin in promoting glucose mobilization during acute hyperosmotic stress in teleost fishes.
Authors:Baltzegar DA, Reading BJ, Douros JD, Borski RJ,
Journal:
PubMed ID:24194509
Osmoregulation is critical for survival in all vertebrates, yet the endocrine regulation of this metabolically expensive process is not fully understood. Specifically, the function of leptin in the regulation of energy expenditure in fishes, and among ectotherms, in general, remains unresolved. In this study, we examined the effects of acute ... More