Notebook Computer Kit for 7300/7500/7500 Fast Real-Time PCR Systems
Notebook Computer Kit for 7300/7500/7500 Fast Real-Time PCR Systems
Applied Biosystems™

Notebook Computer Kit for 7300/7500/7500 Fast Real-Time PCR Systems

Notebook Computer Kit for the Applied Biosystems™ 7500 and 7300 Real-Time PCR Systems.Used With7500 Real-Time PCR System with Dell™ Notebook.For詳細を見る
製品番号(カタログ番号) 4359286
価格(JPY)
Each
お問い合わせください ›
Notebook Computer Kit for the Applied Biosystems™ 7500 and 7300 Real-Time PCR Systems.

Used With
7500 Real-Time PCR System with Dell™ Notebook.

For Research Use Only. Not for use in diagnostics procedures.
For Research Use Only. Not for use in diagnostic procedures.
仕様
使用対象(アプリケーション)Real Time PCR (qPCR)
使用対象 (装置)7300 System, 7500 Fast System, 7500 System
数量1 kit
製品タイプNotebook Computer Kit
Unit SizeEach

よくあるご質問(FAQ)

Applied Biosystems 7500 Real-Time PCR SystemでMultiplex反応を行う場合、リポーター蛍光の組み合わせはどのようにしたらよいでしょうか?

Applied Biosystems 7500 Real-time PCR System または Applied Biosystems 7500 Fast Real-Time PCR System では、MGB-NFQのProbeを使用した場合、以下の蛍光dyeをリポーター蛍光として利用することが可能です [ 注意: TaqMan Gene Expression Master Mix (multiplex解析にはお薦めのMaster Mixです)またはApplied Biosystemsから提供するTaqMan master mixを利用した場合]:
FAM, VIC, JOE, NED, TAMRA,CY3, ROX, TEXAS RED, CY5 dyes.

duplex(2アッセイ)のmultiplex反応を行う場合、 FAM と VICの組合せ、またはFAM と NED の組合せで反応を行うことをお薦めします。またtriplex(3アッセイ)のmultiplex反応を行う場合、 FAM, VIC, Cy5 の組合せ、またはFAM, VIC,TAMRAの組合せで反応を行うことをお薦めします。蛍光の組合せは、お互いの発光波長がなるべく大きく異なる蛍光を選択します。またTAMRAクエンチャー のProbeを使用する場合、Multiplex反応にNED, TAMRA, CY3 は使用できません。ただしApplied Biosystems Master Mix以外の、レファレンス蛍光としてROXを添加していないMaster Mixを使用した場合、 ROX または TEXAS RED が使用できます。

Can TET dye be used on the Applied Biosystems real-time PCR instruments?

TET dye is not recommended to be used on the following real-time PCR instrument models: 7000, 7300, 7500, 7500 FAST, StepOne, and StepOnePlus Systems.

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

What dyes can I use as reporter dyes in a multiplex reaction on the Applied Biosystems 7300 Real-Time PCR Systems?

The Applied Biosystems 7300 Real-Time PCR System has 4 signal detection filters: Filter A (FAM and SYBR Green), Filter B (VIC and JOE), Filter C (TAMRA, NED and Cy3) and Filter D (ROX and Texas Red). For multiplexing reactions, the reporter dyes from the different assays should be chosen from different filter sets, so they can be compatible. In addition, the reporter dye need to be compatible with the quencher and the passive reference dye that might be present in the reaction. The commonly used combination is FAM and VIC.

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

What are the thermal cycling parameters of the Fast mode for the 7500 Fast Real-Time PCR System?

For the 7500 Fast real time PCR systems, the thermal cycling parameters are defaulted to 50°C/2 min for UNG incubation, 95°C/20 sec for fast polymerase activation, 40 cycles of 95°C/3 secs for the dissociation and 60°C/30 seconds for annealing and extensions.

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

Can I run slower, standard thermal cycling experiments on a 7500 Fast Real-Time PCR System?

Yes. you can choose either standard or fast ramp on the 7500 Fast System for software versions 2x or greater, and a 9600 emulation thermal cycling mode is available for customers who wish to run assays based on adjusted ramp rate. However, you should be aware that we cannot guarantee identical performance to the same modes run on a standard 7500 system block.

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

引用および参考文献 (3428)

引用および参考文献
Abstract
Authors:
Journal:
PubMed ID:11282963
Role of APE1 in differentiated neuroblastoma SH-SY5Y cells in response to oxidative stress: Use of APE1 small molecule inhibitors to delineate APE1 functions
Authors:Jiang, YL; Guo, CL; Fishel, ML; Wang, ZY; Vasko, MR; Kelley, MR
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 ... More
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
The time of prenatal immune challenge determines the specificity of inflammation-mediated brain and behavioral pathology.
Authors:Meyer U, Nyffeler M, Engler A, Urwyler A, Schedlowski M, Knuesel I, Yee BK, Feldon J
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 ... More
Preclinical pharmacokinetic and pharmacodynamic evaluation of metronomic and conventional temozolomide dosing regimens.
Authors:Zhou Q, Guo P, Wang X, Nuthalapati S, Gallo JM
Journal:J Pharmacol Exp Ther
PubMed ID:17259446
Metronomic dosed (MD) chemotherapy as opposed to conventional dosed (CD) chemotherapy is considered an alternate strategy to target angiogenesis and limit host toxicity. Although this approach is promising, there has not been any attempt to define optimal metronomic dosing regimens by integrating pharmacokinetic (PK) with pharmacodynamic (PD) measurements. The aim ... More