QIAGEN Multiplex PCR Kit

조건을 잡을 필요없이 쉽고 빠르게 multiplex 분석을 수행 할 수 있습니다

S_1315_AppD_MPPCR0451
상업적인 목적을 위해 제품이 대량으로 필요하거나 맞춤형 또는 최적화 제품이 필요하십니까? QIAGEN에서는 물류, 규정 준수 등에 대한 지원도 제공합니다. QIAGEN에 문의하여 전략적 파트너십과 OEM을 통해 협력하는 방법을 알아보세요

QIAGEN Multiplex PCR Kit (100)

카탈로그 번호 / ID.   206143

For 100 x 50 µl multiplex PCR reactions: 2x QIAGEN Multiplex PCR Master Mix (providing a final concentration of 3 mM MgCl2, 3 x 0.85 ml), 5x Q-Solution (1 x 2.0 ml), RNase-Free Water (2 x 1.7 ml)
₩439,000.00
Product
QIAGEN Multiplex PCR Kit (100)
QIAGEN Multiplex PCR Kit (1000)
QIAGEN Multiplex PCR Kit은/는 분자생물학 분야에 사용하기 위한 것입니다. 이 제품은 질병의 진단, 예방, 또는 치료용이 아닙니다.
상업적인 목적을 위해 제품이 대량으로 필요하거나 맞춤형 또는 최적화 제품이 필요하십니까? QIAGEN에서는 물류, 규정 준수 등에 대한 지원도 제공합니다. QIAGEN에 문의하여 전략적 파트너십과 OEM을 통해 협력하는 방법을 알아보세요

특징

  • 최적화 불필요
  • High specificity and sensitivity with a built-in hot start using HotStarTaq DNA Polymerase
  • 다양한 multiplex PCR applications에 매우 적합
  • 사용하기 쉽고 경제적

제품 세부 정보

The QIAGEN Multiplex PCR Kit is available in a convenient ready-to-use master mix format. The QIAGEN Multiplex PCR Master Mix includes HotStarTaq DNA Polymerase and a unique PCR buffer containing the novel synthetic Factor MP. Together with optimized salt concentrations, this additive stabilizes specifically bound primers and enables efficient extension of all primers in the reaction without the need for optimization. Q-Solution, a novel additive that enables efficient amplification of "difficult" (e.g., GC-rich) templates, is also supplied.

성능

The QIAGEN Multiplex PCR Kit outperformed kits tested from other suppliers and ensures highly specific and sensitive multiplex PCR amplification (see figure " Successful 16-plex PCR "). The kit can be successfully used for various multiplex applications such as typing of transgenic organisms  (see figure " Genotyping transgenic mice") and microsatellite analysis (see figure figure " Successful microsatellite analysis "). The master mix includes HotStarTaq DNA Polymerase for efficient amplification of multiple targets in parallel. Amplfication effiency is further improved by an innovative PCR buffer, also included in the master mix. The unique buffer ensures PCR specificity over a wide range of PCR conditions, minimizing the need for optimization. Suboptimal PCR can be improved with Q-Solution — an additive for the amplification of GC-rich templates — also provided with the kit .

HotStarTaq DNA Polymerase specifications

Concentration: 5 units/µl
Recombinant enzyme: Yes
Substrate analogs: dNTP, ddNTP, dUTP, biotin-11-dUTP, DIG-11-dUTP, fluorescent-dNTP/ddNTP
Extension rate: 2–4 kb/min at 72°C
Half-life: 10 min at 97°C ; 60 min at 94°C
Amplification efficiency: ≥105 fold
5'–>3' exonuclease activity: Yes
Extra A addition: Yes
3'–>5' exonuclease activity: No
Contaminating nucleases: No
Contaminating RNases: No
Contaminating proteases: No
Self-priming activity: No 

그림 참조

원리

The QIAGEN Multiplex PCR Kit is the first kit specifically developed for multiplex PCR and is provided in an easy-to-use master-mix format. QIAGEN Multiplex PCR Master Mix contains preoptimized concentrations of HotStarTaq DNA Polymerase and MgCl2, plus dNTPs and an innovative PCR buffer specially developed for multiplex PCR. The kit enables success in multiplex PCR at the first attempt. There is no need to optimize reaction conditions (e.g., the concentrations of primers, Mg2+, and Taq DNA polymerase) and cycling parameters due to unique preoptimized reagents included in the kit.

HotStarTaq DNA Polymerase

HotStarTaq DNA Polymerase is a modified form of Taq DNA polymerase and has no polymerase activity at ambient temperatures. This prevents extension of nonspecifically annealed primers and primer dimers formed at low temperatures during PCR setup and the initial PCR cycle. HotStarTaq DNA Polymerase is activated by a 15-minute incubation at 95°C which can be incorporated into any existing thermal-cycler program.

Multiplex PCR Buffer

This special buffer contains an optimized combination of K+ and NH4+, as well as the unique PCR additive, Factor MP, which increases the local concentration of primers at the template. Together with K+ and other cations, Factor MP stabilizes specifically bound primers, allowing efficient primer extension by HotStarTaq DNA Polymerase (see figure " Stable and efficient primer annealing"). The innovative buffer maintains specific amplification in every cycle of PCR by promoting a high ratio of specific-to-nonspecific primer binding during the annealing step in each PCR cycle. Owing to a uniquely balanced combination of KCl and (NH4)2SO4, the buffer provides stringent primer-annealing conditions over a wider range of annealing temperatures and Mg2+ concentrations than conventional PCR buffers. Optimization of PCR by varying the annealing temperature or the Mg2+ concentration is therefore often minimal or not required.

Q-Solution

Q-Solution, an innovative PCR additive that facilitates amplification of difficult templates by modifying the melting behavior of DNA, is also provided with HotStarTaq DNA Polymerase. This unique reagent improves suboptimal PCR caused by templates that have a high degree of secondary structure or GC-rich templates. Unlike other commonly used PCR additives such as DMSO, Q-Solution is used at just one working concentration, is nontoxic, and PCR purity is guaranteed.

그림 참조

절차

The QIAGEN Multiplex PCR Kit is provided in a ready-to-use, preoptimized master mix for greater convenience. Use of a master mix saves time, simplifies handling for reaction setup, and increases reproducibility by eliminating many possible sources of pipetting errors and contamination —  pipetting steps are minimized and tedious calculations are eliminated. Only primers and template need to be added to prepare the final amplification mix. The master mix can be stored at 2–8°C, allowing even faster setup of multiplex PCR assays. The streamlined, step-by-step protocol provided with the kit ensures fast and easy PCR setup. Reactions can be set up at room temperature, ensuring greater convenience and ease of use. HotStarTaq DNA Polymerase is activated by a 15-minute, 95°C incubation step, which can easily be incorporated into existing thermal cycling programs.

응용 분야

The QIAGEN Multiplex PCR Kit is highly suited for various multiplex applications, including:

  • Typing and analysis of transgenic organisms
  • Amplification and analysis of microsatellites
  • Typing and detection of bacteria and viruses
  • Amplification of multiple DNA regions for SNP analysis

지원되는 데이터 및 수치

사양

특징사양
applicationsPCR, RT-PCR, multiplex PCR, typing, detection
enzymeactivity5' -> 3' exonuclease activity
reactiontypePCR amplification
withwithouthotstartWith hotstart
singleormultiplexMultiplex
realtimeorendpointEndpoint
mastermixYes
sampletargettypeGenomic DNA and cDNA

리소스

Brochures & Guides en (2)
Second edition — innovative tools
Addressing critical factors and new solutions
Kit Handbooks (1)
For fast and efficient multiplex PCR without optimization
Quick-Start Protocols (1)
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)

출판물

Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing.
Haywood A; Dreau H; Timbs A; Schuh A; Old J; Henderson S;
Ann Hematol; 2010; 89 (12):1215-21 2010 Jun 22 PMID:20567827
Pyrosequencing-based strategy for a successful SNP detection in two hypervariable regions: HV-I/HV-II of the human mitochondrial displacement loop.
Anjum GM; Du W; Klein R; Amara U; Huber-Lang M; Schneider EM; Wiegand P;
Electrophoresis; 2010; 31 (2):309-14 2010 Jan PMID:20084631
In vitro analysis of huntingtin-mediated transcriptional repression reveals multiple transcription factor targets.
Zhai W; Jeong H; Cui L; Krainc D; Tjian R;
Cell; 2005; 123 (7):1241-53 2005 Dec 29 PMID:16377565
Isolation of genomic DNA from buccal swabs for forensic analysis, using fully automated silica-membrane purification technology.
Hanselle T; Otte M; Schnibbe T; Smythe E; Krieg-Schneider F;
Leg Med (Tokyo); 2003; 5 Suppl 1 :S145-9 2003 Mar PMID:12935575