El módulo blot XCell II es un módulo de transferencia húmeda de minigel para los sistemas XCell SureLock o XCellMás información
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Número de catálogo
Cantidad
EI9051
1 unidad
Número de catálogo EI9051
Precio (EUR)
782,00
Each
Añadir al carro de la compra
Cantidad:
1 unidad
Precio (EUR)
782,00
Each
Añadir al carro de la compra
El módulo blot XCell II es un módulo de transferencia húmeda de minigel para los sistemas XCell SureLock o XCell II. El módulo blot XCell II permite transferir fácilmente proteínas o ácidos nucleicos para transferencias Western, Southern y Northern de minigeles a membranas con menos de 200 ml de tampón de transferencia. Los resistentes electrodos platinizados con titanio y acero inoxidable crean un campo eléctrico uniforme sin abrazaderas ni soportes de gel con bisagras. El tamaño del blot máximo es de 9 x 9 cm.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
CapacidadHasta 2 minigeles
Para utilizar con (equipo)XCell SureLock™ Mini
Tamaño de gelMini (8 cm x 8 cm)
Modo de transferenciaHúmedo
Cantidad1 unidad
Dimensión en ejecuciónVertical
Condiciones de envíoTemperatura ambiente
Gel CompatibilityGel Bolt™ Bis-Tris Plus, gel NuPAGE™, minigel Novex™
Línea de productosXCell II
Tipo de productoMódulo blot
Unit SizeEach
Contenido y almacenamiento
El módulo blot XCell II™ incluye núcleo de ánodo, núcleo de cátodo, almohadillas de esponja (8/pack) y manual de instrucciones.
Preguntas frecuentes
Are Bolt gels compatible with transfer devices from other suppliers?
Yes. While we would prefer that you use our devices, Bolt gels can also be transferred using devices from Bio-Rad, including the Mini Trans-Blot Cell, Trans-Blot SD Semi-Dry Transfer Cell, or Trans-Blot Turbo Transfer System.
Do I have to run the XCell Blot Module under cold conditions?
No. The solution placed in the outer chamber serves to dissipate the heat generated during blotting. Water is usually used for this purpose. The recommended transfer conditions generate only a minor heat increase, so it is not necessary to run the unit in an ice bucket or to place it in a cold room. However if you are working with very heat-sensitive proteins, you may wish to do so.
How can I remove residual build-up in the XCell II Blot Module?
Build-up can be removed with 50% nitric acid. Make a solution of 50% nitric acid in deionized water and carefully apply it to areas inside the blot module until residual build-up is removed. Do not submerge the blot module or soak overnight. Use gloves when preparing the solution. Afterwards, rinse the module thoroughly at least three times in fresh deionized water. This treatment should not harm the plastic.
How can residual build-up in the XCell II Blot Module be removed?
Build-up can be removed with 50% nitric acid. Make a solution of 50% nitric acid in deionized water and carefully apply it to areas inside the blot module until residual build-up is removed. Do not submerge the blot module or soak overnight. Use gloves when preparing the solution. Afterwards, rinse the module thoroughly at least three times in fresh deionized water. This treatment should not harm the plastic.
Cercarial Elastase Is Encoded by a Functionally Conserved Gene Family across Multiple Species of Schistosomes.
Authors:Salter Jason P.; Choe Youngchool; Albrecht Hugo; Franklin Christopher; Lim Kee-Chong; Craik Charles S.; McKerrow James H.;
Journal:J Biol Chem
PubMed ID:11986325
Water borne cercaria(ae) of the trematode genus Schistosoma rapidly penetrate host skin. A single serine protease activity, cercarial elastase, is deposited in advance of the invading parasite by holocytosis of vesicles from ten large acetabular gland cells. Cercarial elastase activity is a composite of multiple isoforms. Genes coding for the ... More
Definition of genetically distinct attenuation mechanisms in naturally virulence-attenuated Listeria monocytogenes by comparative cell culture and molecular characterization.
Authors:Roberts A, Chan Y, Wiedmann M,
Journal:Appl Environ Microbiol
PubMed ID:16000803
'Listeria monocytogenes is a foodborne pathogen able to cause serious disease in humans and animals. Not all isolates are equally pathogenic, however, and several isolates have been characterized as naturally virulence attenuated. We sought to identify the genetic basis of natural virulence attenuation using cell culture assays and molecular techniques. ... More
Combined effect of epinephrine and exercise on calpain/calpastatin and cathepsin B and L activity in porcine longissimus muscle.
Authors:Ertbjerg P, Henckel P, Karlsson A, Larsen LM, Møller AJ,
Journal:J Anim Sci
PubMed ID:10492449
The objective of the study was to improve the understanding of the relationship between the effect of epinephrine plus exercise and meat tenderness. The calpain, calpastatin, and cathepsin B + L activities and postmortem proteolysis in porcine longissimus muscle were studied. The muscle glycogen stores were depleted in five pigs ... More
Regulation of the mitogen-activated protein kinase p44 ERK activity during anoxia/recovery in rainbow trout hypodermal fibroblasts.
Authors:Ossum CG, Wulff T, Hoffmann EK,
Journal:J Exp Biol
PubMed ID:16621957
It is well known from various mammalian cells that anoxia has a major impact on the mitogen-activated protein kinase ERK, but a possible similar effect in fish cells has not been investigated. Here we characterise a p44ERK-like protein in the rainbow trout cell line RTHDF and study the effect of ... More
Separate basic region motifs within the adeno-associated virus capsid proteins are essential for infectivity and assembly.
Authors:Grieger JC, Snowdy S, Samulski RJ,
Journal:J Virol
PubMed ID:16699000
Adeno-associated virus (AAV) is gaining momentum as a gene therapy vector for human applications. However, there remain impediments to the development of this virus as a vector. One of these is the incomplete understanding of the biology of the virus, including nuclear targeting of the incoming virion during initial infection, ... More