Dispasa II, polvo
Dispasa II, polvo
Gibco™

Dispasa II, polvo

La dispasa II (proteasa neutra) es una amino-endopeptidasa que hidroliza los enlaces peptídicos aminoterminales de los residuos aminoácidos no polares.Más información
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Número de catálogoCantidad
171050415 g
Número de catálogo 17105041
Precio (CLP)
877.229
Each
Añadir al carro de la compra
Cantidad:
5 g
Precio (CLP)
877.229
Each
Añadir al carro de la compra
La dispasa II (proteasa neutra) es una amino-endopeptidasa que hidroliza los enlaces peptídicos aminoterminales de los residuos aminoácidos no polares. Esta secuencia se encuentra con gran frecuencia en el colágeno. La dispasa II tiene una leve acción proteolítica que resulta útil para el aislamiento y el pasaje rutinario de células primarias. La dispasa II es relativamente suave, se desasocia bien con temperatura y pH fisiológicos y en general mantiene la integridad de la membrana celular.

La dispasa II Gibco™ se produce en Bacillus polymyxa y se envasa en forma de polvo liofilizado no estéril para el uso en estudios de disociación celular o de tejidos y para evitar la aglutinación en cultivos en suspensión. Se garantiza que la actividad de la dispasa II Gibco™ será superior a 0,5 unidades/mg.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Cantidad5 g
Duración de almacenamiento24 meses
Condiciones de envíoTemperatura ambiente
FormularioLiofilizado
Tipo de productoReactivo para disociación de cultivo celular
EsterilidadNo estéril
Unit SizeEach
Contenido y almacenamiento
Condiciones de almacenamiento: de 2 °C a 8 °C. Proteger de la luz
Condiciones de envío: Temperatura ambiente
Vida útil: 24 meses a partir de la fecha de fabricación

Preguntas frecuentes

What is the stability of reconstituted Dispase?

The Dispase solution is stable at -5 to -20 degrees C for a minimum of 1 month.

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

I have Dispase, Cat. No. 17105041. Is it Dispase I or II?

This product is Dispase II.

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

Why is collagenase type IV favored over dispase even though the dissociation with collagenase IV seems to take longer (between 30 and 60 min, depending from the lot, at 37 degrees C) compared to dispase?

Actually, in a feeder-based culture, dispase (2 mg/mL) should take about 15-25 min to work at 37 degrees C. Two to three minutes' dissociation time would apply to feeder-free cultures. Dispase is a more aggressive enzyme, so it works faster, but that also means that when the PSC clumps are harvested, they are more sensitive to being broken apart by trituration. Once the clumps are harvested, they should be pipetted up and down a few times to break up the clumps to the appropriate size. If the cells are harvested with collagenase type IV, they have to be pipetted more times because the clumps are harder to break up, but this means that there is less likelihood to break up the clumps into pieces that are too small. If the cells are harvested with dispase, they have to be pipetted fewer times, and care has to be taken to ensure that the clumps are not broken too much. Either enzyme is fine to use, and if you have enough experience, you may prefer to use dispase to save time. But for a less experienced user, we recommend using collagenase type IV as it is safer and you are less likely to ruin your culture by over-triturating.

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

What reagents do you offer for cell dissociation, and what are the main differences between them?

Please use this selection chart that compares our cell dissociation reagents (https://www.thermofisher.com/us/en/home/life-science/cell-culture/mammalian-cell-culture/reagents/trypsin.html).

Find additional tips, troubleshooting help, and resources within ourMammalian Cell Culture Basics Support Center.

Citations & References (2)

Citations & References
Abstract
Isolation, cultivation and characterization of adult murine prostate stem cells.
Authors:Lukacs RU, Goldstein AS, Lawson DA, Cheng D, Witte ON,
Journal:Nat Protoc
PubMed ID:20360765
'The successful isolation and cultivation of prostate stem cells will allow us to study their unique biological properties and their application in therapeutic approaches. Here we describe step-by-step procedures on the basis of previous work in our laboratory for the harvesting of primary prostate cells from adolescent male mice by ... More
Production of hepatocyte-like cells from human pluripotent stem cells.
Authors:Hannan NR, Segeritz CP, Touboul T, Vallier L,
Journal:Nat Protoc
PubMed ID:23424751
Large-scale production of hepatocytes from a variety of genetic backgrounds would be beneficial for drug screening and to provide a source of cells to be used as a substitute for liver transplantation. However, fully functional primary hepatocytes remain difficult to expand in vitro, and circumventing this problem by using an ... More