Platinum™ II Hot-Start PCR Master Mixes (2X)
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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Catalog NumberNo. of ReactionsColor
14000012Promo Image50 reactionsColorless
14001012Promo Image50 ReactionsGreen
14001013Promo Image200 ReactionsGreen
14001014Promo Image1000 ReactionsGreen
14000014Promo Image1000 reactionsColorless
14000013Promo Image200 ReactionsColorless
Catalog number 14000012
Price (USD)
106.65
Online Exclusive
111.00
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No. of Reactions:
50 reactions
Color:
Colorless
Recurring order eligible. Learn more »
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Price (USD)
106.65
Online Exclusive
111.00
Save 4.35 (4%)
Each
Add to cart
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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.
Specifications
ColorColorless
Concentration2X
Fidelity (vs. Taq)1X
FormatTube
Hot StartBuilt-In Hot Start
No. of Reactions50 reactions
Overhang3'-A
PolymerasePlatinum II Taq Hot-Start DNA Polymerase
Product TypeHot Start PCR Master Mix
Purity or Quality GradeHPLC
Quantity50 reactions
Reaction FormatSuperMix or Master Mix
Shipping ConditionDry Ice
Size (Final Product)5 kb or less
Starting MaterialDNA
For Use With (Application)Hot-start PCR
GC-Rich PCR PerformanceHigh
Reaction SpeedFast or Standard
Unit SizeEach
Contents & Storage
• Platinum II 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.
Have questions about this product? Ask our AI assisted search.
Can Platinum II Taq Hot-Start DNA Polymerase be used in master mixes for qPCR?
With Platinum II Taq Hot-Start DNA Polymerase and Platinum II PCR buffer, how is it possible to use an annealing temperature of 60 degrees C for any primer pair?
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?
Can I use a 2-step cycling protocol with Platinum II Taq Hot-Start DNA Polymerase, combining the annealing and extension steps?
My PCR with Platinum II Taq Hot-Start DNA Polymerase amplifies non-specific products. What are your recommendations?
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Certificates

Lot #Certificate TypeDateCatalog Number(s)
3269008Certificate of AnalysisJun 26, 202514000012
3265988Certificate of AnalysisJun 20, 202514001012
3264933Certificate of AnalysisJun 19, 202514000014
3262726Certificate of AnalysisJun 17, 202514001014
3262541Certificate of AnalysisJun 17, 202514001014
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Safety Data Sheets

Frequently asked questions (FAQs)

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.

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.

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.

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.

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.

Citations & References (15)

Citations & References
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
15 total citations

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