7500 Fast System SDS 21 CFR Part 11 Module
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Applied Biosystems™

7500 Fast System SDS 21 CFR Part 11 Module

The 21 CFR Part 11 Software Module for the 7500 Systems offers the flexibility of user-customizable security configuration settings toWeitere Informationen
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43773551 kit
Katalognummer 4377355
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Menge:
1 kit
The 21 CFR Part 11 Software Module for the 7500 Systems offers the flexibility of user-customizable security configuration settings to assist with 21 CFRp11 compliance.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
Tiefe (angloamerikanisch)17,72 in.
Tiefe (metrisch)45 cm
Zur Verwendung mit (Anwendung)Real Time PCR (qPCR)
Zur Verwendung mit (Geräte)7500 Fast System
Höhe (angloamerikanisch)19,29 in.
Höhe (metrisch)49 cm
Menge1 kit
SoftwaretypSoftware
Thermische Genauigkeit± 25 °C
Temperaturbereich4 °C bis 100 °C
Thermische Gleichmäßigkeit±0,0 °C (30 s nach Taktstart)
Gewährleistung1 Jahr
Gewicht34 kg (75 lb.)
Breite (angloamerikanisch)13,99 in.
Breite (metrisch)34 cm
Blockkonfigurationen96-Well
BlockformatPeltier-basiert
Fassungsvermögen96-Well-Platten (schnell)
Produkttyp7500 System SDS
Unit SizeEach
Inhalt und Lagerung
Pkt. enthält die 21CFRp11-Sequenzerkennungssoftware, Software-CD und Benutzerhandbuch.

Häufig gestellte Fragen (FAQ)

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?

Yes, the standard 7500 instrument has a 96 x 0.2 mL block, whereas the 7500 Fast instrument has a 96 x 0.1 mL block.

Find additional tips, troubleshooting help, and resources within our Real-Time PCR and Digital PCR Instruments Support Center.

Zitierungen und Referenzen (841)

Zitierungen und Referenzen
Abstract
Characterization of matrix metalloproteinase-2 and matrix metalloproteinase-9 and their inhibitors in equine granulosa cells in vivo and in vitro
Authors:Sessions, DR; Vick, MM; Fitzgerald, BP
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 ... More
Molecular cloning and characterization of porcine calcineurin-alpha subunit expression in skeletal muscle.
Authors:Depreux FF, Scheffler JM, Grant AL, Bidwell CA, Gerrard DE
Journal:J Anim Sci
PubMed ID:19897633
The calmodulin/Ca(2+)-dependent serine/threonine phophatase, calcineurin (CaN), has been implicated in controlling muscle fiber phenotype. However, little information is available concerning the expression of CaN in porcine skeletal muscle. Therefore, the porcine CaN alpha (CaN-A) was cloned by reverse transcription-PCR and its expression characterized in selected porcine skeletal muscles. We successfully ... More
Cell lines as candidate reference materials for quality control of ERBB2 amplification and expression assays in breast cancer.
Authors:Xiao Y, Gao X, Maragh S, Telford WG, Tona A
Journal:Clin Chem
PubMed ID:19443566
BACKGROUND: Human epidermal growth factor receptor 2 (HER2) is an important biomarker whose status plays a pivotal role in therapeutic decision-making for breast cancer patients and in determining their clinical outcomes. Ensuring the accuracy and reproducibility of HER2 assays by immunohistochemistry (IHC) and by fluorescence in situ hybridization (FISH) ... More
Genetic analysis of hepatitis C virus with defective genome and its infectivity in vitro.
Authors:Sugiyama K, Suzuki K, Nakazawa T, Funami K, Hishiki T, Ogawa K, Saito S, Shimotohno KW, Suzuki T, Shimizu Y, Tobita R, Hijikata M, Takaku H, Shimotohno K
Journal:J Virol
PubMed ID:19369330
Replication and infectivity of hepatitis C virus (HCV) with a defective genome is ambiguous. We molecularly cloned 38 HCV isolates with defective genomes from 18 patient sera. The structural regions were widely deleted, with the 5' untranslated, core, and NS3-NS5B regions preserved. All of the deletions were in frame, ... More
HIV-1 transactivator protein induction of suppressor of cytokine signaling-2 contributes to dysregulation of IFN{gamma} signaling.
Authors:Cheng SM, Li JC, Lin SS, Lee DC, Liu L, Chen Z, Lau AS
Journal:Blood
PubMed ID:19279332
HIV infection remains a worldwide threat. HIV-1 transactivator protein Tat is one of the retroviral proteins identified as a key immunomodulator in AIDS pathogenesis. Although the primary function of Tat is to regulate HIV-1 replication in the infected cell, it also dysregulates cytokine production resulting in perturbation of the host ... More