Platinum™ II Hot-Start PCR Master Mixes (2X)
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Platinum™ II Hot-Start PCR Master Mixes (2X)
Invitrogen™

Platinum™ II Hot-Start PCR Master Mixes (2X)

Invitrogen Platinum II Hot-Start PCR Master Mix (2X) offers Platinum II Taq Hot-Start DNA Polymerase premixed with Platinum II PCR buffer and dNTPs for convenient PCR setup.
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카탈로그 번호반응 수색상
1400101250 ReactionsGreen
14001013200 ReactionsGreen
140010141000 ReactionsGreen
1400001250 reactionsColorless
140000141000 reactionsColorless
14000013200 ReactionsColorless
카탈로그 번호 14001012
제품 가격(KRW)
118,000
Online offer
Ends: 31-Dec-2025
145,000
할인액 27,000 (19%)
Each
카트에 추가하기
반응 수:
50 Reactions
색상:
Green
대량 주문 또는 맞춤형 요청
제품 가격(KRW)
118,000
Online offer
Ends: 31-Dec-2025
145,000
할인액 27,000 (19%)
Each
카트에 추가하기
Invitrogen Platinum II Hot-Start PCR Master Mix (2X), available in colorless and green formats, offers Platinum II Taq Hot-Start DNA Polymerase premixed with Platinum II PCR buffer and dNTPs for convenient PCR setup. Platinum II Taq Hot-Start DNA Polymerase is designed for universal primer annealing and fast, easy PCR with its unique combination of innovative buffer, high-performance engineered Taq DNA polymerase and leading hot-start technology. This master mix is provided with the optional Platinum GC Enhancer for specific amplification and improved yields of GC-rich targets.

Platinum II Hot-Start Green PCR Master Mix also includes two tracking dyes for direct loading of PCR products on gels.

Features

  • Innovative buffer enables universal annealing temperature by isostabilizing primer-template duplex structures
  • Engineered Taq DNA polymerase confers fast cycling and resistance to common inhibitors
  • Hot-start technology enables superior specificity, sensitivity, and yields and allows for room temperature reaction setup
  • Green PCR buffer reduces pipetting errors with direct gel loading

Applications

  • Amplification of DNA from complex genomic, viral, and plasmid templates
  • Amplification and improved yields of GC-rich targets
  • RT-PCR
  • Genotyping
  • High-throughput PCR

Platinum II Taq Hot-Start DNA Polymerase is an engineered Taq DNA polymerase that shows increased resistance to reaction inhibitors originating from sample material or DNA purification steps. The polymerase has a higher DNA synthesis rate and delivers PCR results more than two times faster than other Taq DNA polymerases. Proprietary Platinum Taq antibodies block polymerase activity at ambient temperatures and dissociate after the initial denaturation step at 94°C. This automatic hot start provides increased sensitivity, specificity, and yield, while allowing reaction assembly at room temperature.

Due to the unique composition of the Platinum II PCR buffer, the annealing temperature is 60°C for most primer pairs designed following the general design rules. Isostabilizing molecules in the buffer increase primer–template duplex stability during the annealing step and contribute to enhanced specificity without the need to optimize annealing temperature for each primer pair. With Platinum II Hot-Start PCR Master Mix (2X), different PCR assays can be cycled together using the same protocol with universal primer annealing temperature and the extension step selected for the longest fragment to be amplified.

Notes

  • For applications that require PCR product analysis by absorbance or fluorescence excitation, colorless format is recommended.
For Research Use Only.
사양
색상Green
Fidelity (Taq 대비)1X
형식Tube
핫 스타트Built-In Hot Start
반응 수50 Reactions
오버행3'-A
중합효소PlatinumTM II Taq Hot-Start DNA Polymerase
제품 유형Hot Start PCR Master Mix
수량50 reactions
반응 형식SuperMix or Master Mix
배송 조건Dry Ice
크기(최종 제품)5 kb or less
시작 물질DNA
농도2X
용도(애플리케이션)Hot-start PCR
GC-Rich PCR PerformanceHigh
반응 속도Fast or Standard
Unit SizeEach
구성 및 보관
• Platinum II Green PCR Master Mix (2X), 1.25 mL
• Platinum GC Enhancer, 1.25 mL
• Nuclease-free water, 1.25 mL

Store at -20°C in a non-frost-free freezer.

자주 묻는 질문(FAQ)

What is the storage temperature of Platinum II Taq Hot-Start DNA Polymerase products?

Platinum II Taq Hot-Start DNA Polymerase products can be stored at 4 degrees C for up to 3 months. For longer storage, we recommend storing all components at -20 degrees C.

Is the PCR product from reactions performed with Platinum II Hot-Start PCR Master Mix and Platinum II Hot-Start Green PCR Master Mix compatible with E-Gel agarose gels?

Electrophoretic separation on E-Gel agarose gels depends on the salt concentration in the analyzed sample. For optimal separation, we recommend diluting PCR reactions performed with colorless and green Platinum II PCR Master Mixes 2- to 20-fold, prior to running on E-Gel agarose gels. The dyes in the Platinum II Hot-Start Green PCR Master Mix do not interfere with fragment separation on E-Gel agarose gels.

Do the dyes in Platinum II Green PCR Buffer interfere with PCR performance of Platinum II Taq Hot-Start DNA Polymerase?

No. The tracing dyes (a blue and a yellow dye) in Platinum II Green PCR Buffer do not interfere with PCR performance and do not change any enzyme features.

Can Platinum II Taq Hot-Start DNA Polymerase be used in master mixes for qPCR?

Yes, Platinum II Taq Hot-Start DNA Polymerase can be used in qPCR master mixes for target detection and quantification in a real-time PCR instrument using probes or SYBR Green dye.

Can I keep my PCR reactions with Platinum II Taq Hot-Start DNA Polymerase at room temperature before the cycling starts?

Yes. Due to stable antibody-mediated hot-start technology, Platinum II Taq Hot-Start DNA Polymerase is highly stable. The premixed reactions for PCR can be incubated at room temperature for up to 24 hr before loading in the thermal cycler, without any loss of amplification specificity.

인용 및 참조 문헌 (15)

인용 및 참조 문헌
Abstract
Monitoring and contamination incidence of gnotobiotic experiments performed in microisolator cages.
Authors:Basic M, Bolsega S, Smoczek A, Gläsner J, Hiergeist A, Eberl C, Stecher B, Gessner A, Bleich A
Journal:Int J Med Microbiol
PubMed ID:33636479
'With the increased interest in the microbiome research, gnotobiotic animals and techniques emerged again as valuable tools to investigate functional effects of host-microbe and microbe-microbe interactions. The increased demand for gnotobiotic experiments has resulted in the greater need for housing systems for short-term maintenance of gnotobiotic animals. During the last ... More
CircINSR Regulates Fetal Bovine Muscle and Fat Development.
Authors:Shen X, Tang J, Ru W, Zhang X, Huang Y, Lei C, Cao H, Lan X, Chen H
Journal:Front Cell Dev Biol
PubMed ID:33490079
'The level of muscle development in livestock directly affects the production efficiency of livestock, and the contents of intramuscular fat (IMF) is an important factor that affects meat quality. However, the molecular mechanisms through which circular RNA (circRNA) affects muscle and IMF development remains largely unknown. In this study, we ... More
Dynamic regulation of connexins in stem cell pluripotency.
Authors:Esseltine JL, Brooks CR, Edwards NA, Subasri M, Sampson J, Séguin C, Betts DH, Laird DW
Journal:Stem Cells
PubMed ID:31646713
'Characterization of the pluripotent "ground state" has led to a greater understanding of species-specific stem cell differences and has imparted an appreciation of the pluripotency continuum that exists in stem cells in vitro. Pluripotent stem cells are functionally coupled via connexins that serve in gap junctional intercellular communication (GJIC) and ... More
Four high-quality draft genome assemblies of the marine heterotrophic nanoflagellate Cafeteria roenbergensis.
Authors:Hackl T, Martin R, Barenhoff K, Duponchel S, Heider D, Fischer MG
Journal:Sci Data
PubMed ID:31964893
'The heterotrophic stramenopile Cafeteria roenbergensis is a globally distributed marine bacterivorous protist. This unicellular flagellate is host to the giant DNA virus CroV and the virophage mavirus. We sequenced the genomes of four cultured C. roenbergensis strains and generated 23.53?Gb of Illumina MiSeq data (99-282?×?coverage per strain) and 5.09?Gb of ... More
Generation of an induced pluripotent stem cell line (TRNDi008-A) from a Hunter syndrome patient carrying a hemizygous 208insC mutation in the IDS gene.
Authors:Hong J, Xu M, Li R, Cheng YS, Kouznetsova J, Beers J, Liu C, Zou J, Zheng W
Journal:Stem Cell Res
PubMed ID:31071499
'Mucopolysaccharidosis Type II (MPS II), also known as Hunter syndrome, is a rare X-linked genetic disease caused by mutations in the IDS gene encoding iduronate 2-sulfatase (I2S). This is a multisystem disorder with significant variation in symptoms. Here, we document a human induced pluripotent stem cell (iPSC) line generated from ... More