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Citations & References (841)
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 to詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| 4377355 | 1 kit |
製品番号（カタログ番号） 4377355
価格（JPY）お問い合わせください ›
Each
数量:
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.
研究用途にのみご使用ください。診断目的には使用できません。
仕様
奥行き（ヤードポンド法）17.72 in.
奥行き（メートル法）45 cm
使用対象（アプリケーション）Real Time PCR (qPCR)
使用対象 (装置)7500 Fast System
高さ（ヤードポンド法）19.29 in.
高さ（メートル法）49 cm
数量1 kit
ソフトウェアタイプSoftware
熱確度±0.0.25°C
熱範囲4°C to 100°C
熱均一性±0.0°C (30 s after Clock Start)
保証1 Year
重量34 kg (75 lb.)
幅（ヤードポンド法）13.99 in.
幅（メートル法）34 cm
ブロック構成96-well
ブロックフォーマットPeltier-based
容量96-well Plate (Fast)
製品タイプ7500 System SDS
Unit SizeEach
組成および保存条件
Pk. includes 21 CFRp11 Sequence Detection Software, software CD, and user guide.
よくあるご質問（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?
引用および参考文献 (841)
引用および参考文献
Abstract
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
Molecular cloning and characterization of porcine calcineurin-alpha subunit expression in skeletal muscle.
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
Cell lines as candidate reference materials for quality control of ERBB2 amplification and expression assays in breast cancer.
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)
Genetic analysis of hepatitis C virus with defective genome and its infectivity in vitro.
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,
HIV-1 transactivator protein induction of suppressor of cytokine signaling-2 contributes to dysregulation of IFN{gamma} signaling.
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