Taq PCR Core Kit

For standard and specialized PCR applications, includes dNTP mix

S_1279_7_LS_OEM_Taq_PCR_Core_Kit_1000
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

Taq PCR Core Kit (1000 U)

카탈로그 번호 / ID.   201225

4 x 250 units Taq DNA Polymerase, 10x PCR Buffer, 10x CoralLoad PCR Buffer, 5x Q-Solution, 25 mM MgCl2, dNTP Mix
수량
1000 U
250 U
Taq PCR Core 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

  • QIAGEN PCR Buffer for minimal optimization
  • 빠르고 편리함을 제공하는 CoralLoad PCR loading buffer가 들어있음
  • 혁신적인 Q-Solution으로 GC-rich templates 또는 extensive secondary structure template도 증폭가능
  • 쉽고 간편한 조작을위해 format 선택이 가능함

제품 세부 정보

Taq PCR Core Kit is provided in a complete kit format comprising, Taq DNA Polymerase, the unique QIAGEN PCR Buffer that minimizes the requirement for optimization, as well as a dNTP mix. Also provided is Q-Solution, a novel additive that enables efficient amplification of "difficult" (e.g., GC rich) templates. In addition, CoralLoad PCR Buffer (containing two gel-tracking dyes) is included, enabling immediate loading of PCR products.

성능

The Taq PCR Core Kit outperformed kits tested from other suppliers and delivers robust PCR performance in a wide range of PCR applications — without the need for time-consuming optimization. The kit includes Taq DNA Polymerase, a high-quality recombinant enzyme that is suitable for general and specialized PCR applications (see figures " Tolerance of different primer Tm Values" and " Specific amplification of long PCR products"). Every lot of Taq DNA Polymerase is subjected to a comprehensive range of quality control tests, including a stringent PCR specificity and reproducibility assay in which low-copy targets are amplified from human genomic DNA (see figure " Lot-to-lot reproducibility"). The unique formulation of QIAGEN PCR Buffer and CoralLoad PCR Buffer, also provided with the kit, enable highly specific PCR in a variety of PCR conditions with minimal optimization requirements (see figures " Wide annealing-temperature window" and " Tolerance to variable magnesium concentration"). In addition, CoralLoad PCR Buffer enables immediate loading of PCR products onto an agarose gel for even easier handling and faster results. Suboptimal PCR can be improved using Q-Solution, a PCR additive, also provided with the kit (see figure " Amplification of difficult templates").

Taq 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

TheTaq PCR Core Kit includes everything required for convenient and reliable PCR —Taq DNA Polymerase, QIAGEN PCR Buffer, CoralLoad PCR Buffer, Q-Solution, dNTP Mix, and MgCl2.

Taq DNA Polymerase

Taq DNA Polymerase is a high-quality recombinant enzyme that is suitable for general and specialized PCR applications (see figures " Tolerance of different primer Tm values" and " Specific amplification of long PCR products").

QIAGEN PCR Buffer

The innovative QIAGEN PCR Buffer has been developed to save time and effort by reducing the need for PCR optimization. QIAGEN PCR Buffer contains both KCl and (NH4)2SO4 (see figure " Increased specificity of primer annealing"). This unique buffer facilitates the amplification of specific PCR  products. During the annealing step of every PCR cycle, the buffer allows a high ratio of specific-to-nonspecific primer binding. Owing to a uniquely balanced combination of KCl and (NH4)2SO4, the PCR 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 dramatically reduced and often not required (see figures " Wide annealing temperature window" and " Tolerance to variable magnesium concentration").

CoralLoad PCR Buffer

CoralLoad PCR Buffer has all the advantages of QIAGEN PCR Buffer. In addition, it can also be used to directly load the PCR reaction onto an agarose gel — separate addition of a gel loading buffer is not required. CoralLoad PCR Buffer provides the same high PCR specificity and minimal reaction optimization as the conventional QIAGEN PCR Buffer. Additionally, it contains two marker dyes — an orange dye and a red dye — that facilitate estimation of DNA migration distance and optimization of agarose gel run time (see figure " CoralLoad PCR Buffer"). The buffer ensures improved pipetting visibility and enables direct loading of PCR products onto a gel, for enhanced convenience.

Q-Solution

Q-Solution facilitates amplification of GC-rich templates or templates with a high degree of secondary structure by modifying the melting behavior of DNA. Use of this unique reagent often enables or improves suboptimal PCR (see figure " Amplification of difficult templates"). Unlike DMSO and other PCR additives, Q-Solution is used at a defined working concentration with any primer–template system and is not toxic.

그림 참조

절차

The Taq PCR Core Kit provides all the components required to set up a PCR and can be used for a multitude of PCR-based applications. The optimized, easy-to-follow, streamlined protocol provided with the kit ensures successful PCR results. Suboptimal PCR is simplified with Q-Solution, a unique PCR additive, also included with the kit.

응용 분야

Taq DNA Polymerase is used for standard and specialized applications, including:

  • General PCR
  • RT-PCR
  • Screening
  • PCR-based DNA fingerprinting (VNTR, STR, and RAPD)

지원되는 데이터 및 수치

사양

특징사양
applicationsPCR, RT-PCR, DNA fingerprinting
sampletargettypeGenomic DNA and cDNA
realtimeorendpointEndpoint
dntpsincludedYes
singleormultiplexSingle
reactiontypePCR amplification
mastermixNo
withwithouthotstartWithout hotstart
enzymeactivity5' -> 3' exonuclease activity

리소스

Brochures & Guides en (2)
Second edition — innovative tools
Addressing critical factors and new solutions
Quick-Start Protocols (1)
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.
Brochures & Guides (1)
Kit Handbooks (1)
For standard and specialized PCR applications with minimal optimization
Certificates of Analysis (1)

출판물

Combined real-time PCR and rpoB gene pyrosequencing for rapid identification of Mycobacterium tuberculosis and determination of rifampin resistance directly in clinical specimens.
Halse TA; Edwards J; Cunningham PL; Wolfgang WJ; Dumas NB; Escuyer VE; Musser KA;
J Clin Microbiol; 2010; 48 (4):1182-8 2010 Jan 27 PMID:20107097
Expression of calcium channels along the differentiation of cultured trophoblast cells from human term placenta.
Moreau R; Hamel A; Daoud G; Simoneau L; Lafond J;
Biol Reprod; 2002; 67 (5):1473-9 2002 Nov PMID:12390878
An immune evasion mechanism for spirochetal persistence in Lyme borreliosis.
Liang FT; Jacobs MB; Bowers LC; Philipp MT;
J Exp Med; 2002; 195 (4):415-22 2002 Feb 18 PMID:11854355