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KK1006

Roche

KAPA Taq ReadyMix

2 ×, suitable for PCR

Synonym(s):

PCR, taq

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About This Item

UNSPSC Code:
41106300
NACRES:
NA.54

usage

50 μL sufficient for 250 reactions

Quality Level

shelf life

≤18 mo.

feature

dNTPs included
hotstart: no

packaging

pkg of 6.25 mL

manufacturer/tradename

Roche

concentration

2 ×

technique(s)

PCR: suitable

input

purified DNA

storage temp.

−20°C

General description

KAPA Taq ReadyMix (2X) is a ready-to-use cocktail containing all components for polymerase chain reaction (PCR), except primers and template. KAPA Taq ReadyMix is available with and without dye. The 2X ReadyMix with dye contains two inert tracking dyes to enable direct loading of PCR products onto agarose gels for analysis by electrophoresis, without the need to add a DNA loading solution. KAPA Taq DNA Polymerase is based on the single-subunit, wild-type Taq DNA polymerase of the thermophilic bacterium Thermus aquaticus.

Application

KAPA Taq ReadyMix has been used in:
  • high throughput PCR
  • amplification of low copy DNA templates
  • multiplex PCR
  • specific amplification of complex templates
  • RT-PCR
  • as a component of the reaction mixture for polymerase chain reaction (PCR) and for cDNA amplification

Biochem/physiol Actions

KAPA Taq and KAPA Taq HotStart® DNA Polymerase elicit 5′-3′ polymerase and 5′-3′ exonuclease activities, but no 3′-5′ exonuclease (proofreading) activity. The enzymes exhibit an error rate of approximately 1 error per 2.2 X 105 nucleotides incorporated. In hot start formulation, the KAPA Taq associates with a proprietary antibody that inactivates the enzyme until the first denaturation step, eliminating spurious amplification products and increasing reaction efficiency and sensitivity. PCR products generated with KAPA Taq are A-tailed and are suitable for cloning into TA cloning vectors.

Features and Benefits

High performance:
  • Improved sensitivity, specificity, and yields
  • Novel buffer formulation facilitates specific primer annealing, leading to higher yield of specific product

Quick Notes:
  • KAPA Taq ReadyMix can replace any commercial Taq DNA polymerase in an existing protocol. The annealing temperature may need to be optimized to account for differences in formulation.
  • The KAPA Taq PCR system is suitable for the amplification of fragments up to 3.5 kb from genomic DNA or 5 kb from less complex targets.
  • The 2X KAPA Taq ReadyMix with dye includes two inert tracking dyes, which allow loading of PCR products directly onto agarose gels for analysis.
  • KAPA Taq ReadyMixes contain 1.5 mM MgCl2 and 0.2 mM of each dNTP (at 1X).

Quality

Each batch of KAPA Taq DNA Polymerase is confirmed to contain <2% contaminating protein (Agilent Protein 230 Assay). KAPA Taq ReadyMixes are subjected to stringent quality control tests, are free of contaminating exo- and endonuclease activity, and meet strict requirements with respect to DNA contamination levels.

Preparation Note

Always ensure that the product has been fully thawed and mixed before use. Reagents may be stored at 4°C for short-term use (up to 1 month). Return to -20°C for longterm storage

Other Notes

For Research Use Only. Not for use in diagnostic procedures.

Legal Information

HOTSTART is a registered trademark of Molecular BioProducts, Inc.
ReadyMix is a trademark of Sigma-Aldrich Co. LLC

Kit Components Only

Product No.
Description

  • KAPA Taq Standard or HotStart® DNA Polymerase 5 U/μL

  • 10X KAPA Taq Buffer A

  • 10X KAPA Taq Buffer B

  • 10X KAPA Buffer

  • 5X KAPA Taq HotStart® Buffer (HotStart® kits only)

  • MgCl2 25 mM

  • dNTP Mix (optional) 10 mM each

  • Stabilizers

See All (8)

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Meesbah Jiwaji et al.
PloS one, 14(6), e0217494-e0217494 (2019-06-05)
Emerging viral diseases, most of which are zoonotic, pose a significant threat to global health. There is a critical need to identify potential new viral pathogens and the challenge is to identify the reservoirs from which these viruses might emerge.
Effects of inoculating Lachnum and Cadophora isolates on the growth of Vaccinium corymbosum.
Bizabani C and Dames J
Microbiological research, 181, 68-74 (2015)
W Malherbe et al.
International journal for parasitology. Parasites and wildlife, 10, 207-210 (2019-11-02)
This study reports on the first evidence of genomic material of the causative agent for epizootic ulcerative syndrome (EUS), Aphanomyces invadans, from fish in the Limpopo River system and the Kruger National Park, South Africa. Fourteen fish species were collected
Expanding the host range of small insect RNA viruses: Providence virus (Carmotetraviridae) infects and replicates in a human tissue culture cell line.
Jiwaji M, et al.
The Journal of General Virology, 97(10), 2763-2768 (2016)
Mariska R Greeff et al.
Diseases of aquatic organisms, 99(2), 103-117 (2012-06-14)
Abalone Haliotis midae exhibiting typical clinical signs of tubercle mycosis were discovered in South African culture facilities in 2006, posing a significant threat to the industry. The fungus responsible for the outbreak was identified as a Peronosporomycete, Halioticida noduliformans. Currently

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