Rat (Sprague-Dawley) Cryopreserved Hepatocytes, Plateable Male
Gibco™
Rat (Sprague-Dawley) Cryopreserved Hepatocytes, Plateable Male
Estos hepatocitos criopreservados plaqueables de rata macho (Sprague - Dawley) se han caracterizado para actividades enzimáticas de metabolización de fármacosMás información
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Número de catálogo
Cantidad
RTCP10
1 vial
Número de catálogo RTCP10
Precio (CLP)
-
Cantidad:
1 vial
Estos hepatocitos criopreservados plaqueables de rata macho (Sprague - Dawley) se han caracterizado para actividades enzimáticas de metabolización de fármacos en fase I y fase II.
Células por vial: Entre 4 y 8 millones
Consiga los resultados que necesita con los hepatocitos GIBCO Los hepatocitos de alta calidad y alta viabilidad, con una morfología celular adecuada y actividad metabólica aumentan la capacidad de dibujar correlaciones in vitro⁄in vivo y de tomar decisiones sólidas con respecto al destino de un compuesto. Los técnicos experimentados y las técnicas de aislamiento exclusivas combinados con las estrictas especificaciones de liberación garantizan que usted reciba los hepatocitos crioconservados de la más alta calidad.
Cada lote se prueba para: • Viabilidad ≥ 75 % • Eficacia de los accesorios • Formación de monocapas e integridad • Confluencia > 80 % al quinto día • Actividades enzimáticas en fase Isolo
Solo para uso en investigación. No diseñado para uso diagnóstico o terapéutico en humanos ni en animales.
Nota: Estos productos requieren envío en recipientes Dewar de vapor LN2, por lo tanto, pueden aplicarse cargos adicionales.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Fuente de dadoresAgrupadas
N.° de celdas4-8 x 10^6
Línea de productosGibco
Tipo de productoHepatocitos
Cantidad1 vial
Tipo de célulaCélula de hepatocitos
FormularioCrioconservado
SexoHombre
EspecieRata
Unit SizeEach
Contenido y almacenamiento
Almacenar en un recipiente Dewar de crioalmacenamiento o en un congelador a - 135 °C.
Preguntas frecuentes
Who can I call if I have technical questions regarding cryopreserved hepatocytes?
Thermo Fisher Scientific has a dedicated team to answer questions regarding hepatocytes. You can send a question by email (hepaticproducts@thermofisher.com) or contact us by phone: US toll-free: (866) 952 3559
With my hepatocytes, I'm seeing rounding up of the cells, cellular debris, and/or holes in the monolayer, indicating dying cells. What should I do?
This could be due to the toxicity of the test compound. Here are other potential causes and recommendations:
-Sub-optimal culture medium: Use Williams Medium E with Plating and Incubation Supplement Packs; refer to our plating protocol
-Hepatocyte lot not characterized as plateable: Check lot specifications to ensure it is qualified for plating
-Cells were cultured for too long: In general, plateable cryopreserved hepatocytes should not be cultured for more than five days
I'm getting unexpected induction results with my hepatocytes. What could be causing this?
First of all, we recommend comparing results to those reported on our lot-specific characterization specification sheet (human cells) and also referring to our enzyme induction protocol. Here are other potential causes and recommendations:
-Sub-optimal monolayer confluency: Please see our recommendations for 'I have a sub-optimal monolayer confluency for my hepatocytes. What should I do?'
-Poor monolayer integrity: Please see our recommendations for 'With my hepatocytes, I’m seeing rounding up of the cells, cellular debris, and/or holes in the monolayer, indicating dying cells. What should I do?'
-Inappropriate positive control: Check positive control to ensure suitability
-Incorrect concentration of positive control: Use the correct concentration of positive control
I'm seeing sub-optimal bile canlicular formation with my hepatocytes. What should I do?
Please see the following causes and recommendations:
-Hepatocyte lot not transporter-qualified: Check lot specifications to ensure it is transporter-qualified
-Sub-optimal culture medium: Use Williams Medium E with Plating and Incubation Supplement Packs; refer to our plating protocol
-Not enough time for bile canaliculi to form: In general, at least 4-5 days in culture is required for bile canalicular network formation
I'm getting a loss of membrane integrity or cuboidal cell shape with my hepatocytes. What should I do?
Please see the following causes and recommendations:
-Hepatocyte lot not characterized as plateable: Check lot specifications to ensure it is qualified for plating
-Sub-optimal culture medium: Use Williams Medium E with Plating and Incubation Supplement Packs; refer to our plating protocol
-Cells were cultured for too long: In general, plateable cryopreserved hepatocytes should not be cultured for more than five days