Agarosa UltraPure™-1000
Agarosa UltraPure™-1000
Citas y referencias (6)
Invitrogen™

Agarosa UltraPure™-1000

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La agarosa-1000 UltraPure™ es un polisacárido (consulte la estructura) utilizado para la separación basada en el tamaño de ácidos nucleicosMás información
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Número de catálogoCantidad
16550100100 g
Número de catálogo 16550100
Precio (USD)
574,05
Each
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Cantidad:
100 g
Pedido a granel o personalizado
Precio (USD)
574,05
Each
Añadir al carro de la compra
La agarosa-1000 UltraPure™ es un polisacárido (consulte la estructura) utilizado para la separación basada en el tamaño de ácidos nucleicos en electroforesis de gel de agarosa. La agarosa 1000 UltraPure™ está específicamente formulada para la separación de fragmentos pequeños (<1000 bp) de ADN, ARN y PCR de alta resolución. Esta agarosa de temperatura de fusión estándar puede resolver diferentes fragmentos de ADN en tan solo 10 pb de tamaño. Ventajas de utilizar la agarosa 1000 Ultrapure™:

• Ideal para el análisis y la recuperación de fragmentos pequeños de ADN y ARN
• La fuerte estructura de gel permite una mejor manipulación
• Una mejor claridad permite una mayor visibilidad de los fragmentos

Envase mejorado
El nuevo envase ecológico utiliza un 75 % menos de plástico que los frascos originales (consulte la figura). Por lo tanto, se emplean menos materias primas y energía en la fabricación, y se generan menos residuos. Además, la boquilla de fácil uso reduce la probabilidad de que se produzcan derrames y contaminación.

Pruebas de rendimiento y calidad
El rendimiento de la agarosa 1000 UltraPure™ se evalúa para satisfacer las especificaciones de apariencia, humedad, resistencia del gel, temperatura de gelificación, temperatura de fusión, contenido de sulfato, electroendósmosis y ensayo de ADNasa/ARNasa.

Nota: Agarosa 10 000 Ultrapure™ (de cat. de cat. 16550-100) es un sustituto de un artículo que se vendía previamente con el n.º de cat. 10975-035.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Para utilizar con (aplicación)Electroforesis en gel de ácidos nucleicos, Blotting
FormularioPolvo
Compatibilidad del gelGeles de agarosa
Características ecológicasEmbalaje sostenible
Punto de fusiónPunto de fusión estándar
Línea de productosUltrapuro
Tipo de productoAgarosa
Cantidad100 g
Condiciones de envíoTemperatura ambiente
Intervalo de separaciónDe 50 bp a 1 kb
Unit SizeEach
Contenido y almacenamiento
1 bolsa con 100 g de agarosa UltraPure™ de punto de fusión bajo. Almacenar a temperatura ambiente.

Preguntas frecuentes

I want to pour my own gels. Which agarose should I use?

Our UltraPure Agarose is standard melting-point agarose designed for routine separation and analysis of DNA and RNA fragments in the 500-23,000 nt range. UltraPure Agarose 1000 is a specialized agarose that provides higher resolution of PCR fragments and other short DNA fragments. We also offer an UltraPure Low Melting Point Agarose, which is ideal for resolving DNA fragments from 10 to 1,000 bp with a low melting temperature of 65°C or less.

How can generation of replication competent adenoviruses be avoided when using your pSilencer adeno 1.0-CMV System?

Although there is only a very small chance of creating replication competent virus, steps should still be taken to avoid added risk. The virus is expanded in two rounds of amplification, and all secondary expansions should be performed from an initial expansion stock. Secondary amplifications in HEK293 cells should not be performed from the stock of another secondary expansion, as this could increase the chance of making replication competent virus. See the product manual for more detail and guidelines for screening.

Find additional tips, troubleshooting help, and resources within our RNAi Support Center.

Citations & References (6)

Citations & References
Abstract
Co-injection of a targeted, reversibly masked endosomolytic polymer dramatically improves the efficacy of cholesterol-conjugated small interfering RNAs in vivo.
Authors:Wong SC, Klein JJ, Hamilton HL, Chu Q, Frey CL, Trubetskoy VS, Hegge J, Wakefield D, Rozema DB, Lewis DL
Journal:Nucleic Acid Ther
PubMed ID:23181701
'Effective in vivo delivery of small interfering (siRNA) has been a major obstacle in the development of RNA interference therapeutics. One of the first attempts to overcome this obstacle utilized intravenous injection of cholesterol-conjugated siRNA (chol-siRNA). Although studies in mice revealed target gene knockdown in the liver, delivery was relatively ... More
Relationship of IL-1 and TNF-a polymorphisms with Helicobacter pylori in gastric diseases in a Brazilian population.
Authors:Santos JC, Ladeira MS, Pedrazzoli J, Ribeiro ML
Journal:Braz J Med Biol Res
PubMed ID:22714811
'It is well known that the risk of development of gastric cancer (GC) in Helicobacter pylori-infected patients depends on several factors. Thus, the aim of this study was to investigate the effect of proinflammatory cytokine gene polymorphisms for IL-1ß, IL-1RN and TNF-a on the development of GC in a Brazilian ... More
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population.
Authors:de Oliveira JG, Silva AE
Journal:World J Gastroenterol
PubMed ID:22468087
'To investigate toll-like receptor 2 (TLR2) -196 to -174 del, and TLR4 (+896A/G rs4986790 and +1196C/T rs4986791) polymorphisms at risk of chronic gastritis and gastric cancer in a Brazilian population and association of gastric lesions with risk factors such as smoking, alcohol intake and Helicobacter pylori infection.' ... More
Transcriptome characterization and gene expression of Epinephelus spp in endoplasmic reticulum stress-related pathway during betanodavirus infection in vitro.
Authors:Lu MW, Ngou FH, Chao YM, Lai YS, Chen NY, Lee FY, Chiou PP
Journal:BMC Genomics
PubMed ID:23170826
'Grouper (Epinephelus spp) is an economically important fish species worldwide. However, viral pathogens such as nervous necrosis virus (NNV) have been causing severe infections in the fish, resulting in great loss in the grouper aquaculture industry. Yet, the understanding of the molecular mechanisms underlying the pathogenicity of NNV is still ... More
A non-exothermic cell-embedding tissue-mimicking material for studies of ultrasound-induced hyperthermia and drug release.
Authors:Mylonopoulou E, Bazán-Peregrino M, Arvanitis CD, Coussios CC
Journal:Int J Hyperthermia
PubMed ID:23406389
'The present study aims to create and characterise a cell-embedding tissue-mimicking material (TMM) that has thermal and acoustic properties similar to liver tissue, in order to enable study and optimisation of protocols for ultrasound-induced hyperthermia and drug delivery.' ... More
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