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Merck

TAQHSKB

Roche

KAPA Taq HotStart

Synonym(e):

PCR, taq

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About This Item

UNSPSC-Code:
41106300
NACRES:
NA.55

Verwendung

sufficient for 1000 reactions
sufficient for 500 reactions
sufficient for 5000 reactions

Qualitätsniveau

Haltbarkeit

≤18 mo.

Leistungsmerkmale

dNTPs included: no
hotstart

Verpackung

pkg of 250 U (KK1508)
pkg of 2500 U (KK1513)
pkg of 500 U (KK1510)

Hersteller/Markenname

Roche

Methode(n)

PCR: suitable

Aufnahme

purified DNA

Lagertemp.

−20°C

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Anwendung

KAPA Taq HotStart® has been used for:
  • High throughput PCR
  • Amplification of low copy DNA templates
  • Multiplex PCR
  • Specific amplification of complex templates
  • RT-PCR
  • confronting two-pair primers-polymerase chain reaction (CTPP-PCR)
  • end-point PCR

Biochem./physiol. Wirkung

KAPA Taq DNA Polymerase is based on the single-subunit, wild-type Taq DNA polymerase of the thermophilic bacterium Thermus aquaticus. KAPA Taq and KAPA Taq HotStart® DNA Polymerase have 5′→3′ polymerase and 5′→3′ exonuclease activities, but no 3′ → 5′ exonuclease (proofreading) activity. The enzyme has an error rate of approximately 1 error per 2.2 x 105 nucleotides incorporated. In the HotStart formulation, the KAPA Taq is combined with a proprietary antibody that inactivates the enzyme until the first denaturation step, eliminating spurious amplification products and increasing reaction efficiency and sensitivity.

Leistungsmerkmale und Vorteile

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 HotStart® DNA Polymerase can replace any commercial hotstart Taq DNA polymerase in an existing protocol. The final MgCl2 concentration and annealing temperature may need to be optimized to account for differences in formulation.
  • The KAPA Taq HotStart Buffer is a uniquelyformulated buffer offering improved specificity and sensitivity, and improved amplification of GC- and AT-rich templates.
  • The KAPA Taq HotStart Buffer does not contain MgCl2; MgCl2 (25 mM) is supplied separately to allow greater flexibility during reaction setup.
  • The KAPA Taq HotStart PCR Kit is suitable for the amplification of fragments up to 3.5 kb from genomic DNA or 5 kb from less complex targets.

Qualität

Each batch of KAPA Taq HotStart® DNA Polymerase is confirmed to contain <2% contaminating protein (Agilent Protein 230 Assay). KAPA Taq HotStart PCR kits 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.

Angaben zur Herstellung

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 long term storage.

Sonstige Hinweise

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

Rechtliche Hinweise

HOTSTART is a registered trademark of Molecular BioProducts, Inc.

Nur Kit-Komponenten

Produkt-Nr.
Beschreibung

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

  • 10X KAPA Taq Buffer A

  • 10X KAPA Taq Buffer B

  • 10X KAPA Buffer with loading dye (optional)

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

  • MgCl2 25 mM

Piktogramme

Exclamation markHealth hazard

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral - STOT SE 2

Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

WGK 1

Flammpunkt (°F)

does not flash

Flammpunkt (°C)

does not flash


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Aquaculture (Amsterdam, Netherlands), 412, 14-22 (2013)
The VNTR 48 bp polymorphism in the DRD4 gene is associated with higher tobacco smoking in male Mexican mestizo smokers with and without COPD
Perez-Rubio G, et al.
Diagnostics (Basel, Switzerland), 10 (2020)
Confronting two biomolecular techniques to detect NRF2 gene polymorphism biomarkers
Chiarella P, et al.
Future science OA, 5 (2018)

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