Search
Citas y referencias (1594)
Applied Biosystems™
7500 System SDS 21 CFR Part 11 Module
The new 21 CFR Part 11 Module for the 7500 Real-Time PCR System offers the flexibility of user-customizable CFR configurationMás información
| Número de catálogo | Cantidad |
|---|---|
| 4377354 | 1 kit |
Número de catálogo 4377354
Precio (MXN)
-
Cantidad:
1 kit
The new 21 CFR Part 11 Module for the 7500 Real-Time PCR System offers the flexibility of user-customizable CFR configuration settings to assist in compliance with the Code of Federal Regulations Title 21 Part 11.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Fondo (imperial)17.72 in.
Fondo (métrico)45 cm
Para utilizar con (aplicación)PCR en tiempo real (PCRq)
Para utilizar con (equipo)Sistema 7500
Altura (imperial)19.29 in.
Altura (métrico)49 cm
Cantidad1 kit
Tipo de softwareSoftware
Exactitud térmica± 0,0/25 °C
Intervalo térmicoDe 4 °C a 100 °C
Uniformidad térmica± 0,0 °C (30 s después de iniciar el reloj)
Garantía1 Year
Peso34 kg (75 lb.)
Anchura (imperial)13.99 in.
Anchura (métrico)34 cm
Configuraciones de bloques96-well
Formato de bloquePeltier-based
Capacidad96-well Plate x 0.2 mL Tubes
Tipo de producto7500 System SDS
Unit SizeEach
Preguntas frecuentes
Are there differences in the tube/plate format between Applied Biosystems 7500 Real-Time PCR Systems and Applied Biosystems 7500 Fast Real-Time PCR Systems?
Citations & References (1594)
Citations & References
Abstract
Role of APE1 in differentiated neuroblastoma SH-SY5Y cells in response to oxidative stress: Use of APE1 small molecule inhibitors to delineate APE1 functions
Journal:DNA REPAIR
PubMed ID:
Oxidative DNA damage has been implicated in a number of central nervous system pathologies. The base excision repair (BER) pathway is one of the most important cellular protection mechanisms that respond to oxidative DNA damage. Human apurinic (apyrimidinic) endonuclease/redox effector factor (APE1/Ref1 or APE1) is an essential enzyme in the
Characterization of matrix metalloproteinase-2 and matrix metalloproteinase-9 and their inhibitors in equine granulosa cells in vivo and in vitro
Journal:JOURNAL OF ANIMAL SCIENCE
PubMed ID:
Matrix metalloproteinases (MMP) and tissue inhibitors of MMP (TIMP) regulate tissue remodeling events necessary for ovulation. Thus, changes in MMP and TIMP expression and protein enzyme activity were examined in vivo and in vitro during follicular development and atresia in the horse. Equine granulosa cells and follicular fluid from medium
The time of prenatal immune challenge determines the specificity of inflammation-mediated brain and behavioral pathology.
Journal:J Neurosci
PubMed ID:16672647
Disturbance to early brain development is implicated in several neuropsychiatric disorders including autism, schizophrenia, and mental retardation. Epidemiological studies have indicated that the risk of developing these disorders is enhanced by prenatal maternal infection, presumably as a result of neurodevelopmental defects triggered by cytokine-related inflammatory events. Here, we demonstrate that
Distinct roles for IFN regulatory factor (IRF)-3 and IRF-7 in the activation of antitumor properties of human macrophages.
Journal:Cancer Res
PubMed ID:17079482
When properly activated, macrophages can be tumoricidal, thus making them attractive additions to standard cancer therapies. To this end, tolerance and activity of human autologous IFN-gamma-activated macrophages, produced in large scale for clinical use (MAK cells), have been assessed in pilot trials in cancer patients. In the present study, we
Trps1 plays a pivotal role downstream of Gdf5 signaling in promoting chondrogenesis and apoptosis of ATDC5 cells.
Journal:Genes Cells
PubMed ID:18363966
Tricho-rhino-phalangeal syndrome (TRPS) is an autosomal dominant skeletal disorder caused by mutations of TRPS1. Based on the similar expression patterns of Trps1 and Gdf5, we hypothesized a possible functional interaction between these two molecules. Using a chondrogenic cell line (ATDC5), we investigated the association of Gdf5-mediated signaling pathways with