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Key Documents

TAQKB

Roche

KAPA Taq PCR Kit

Synonyme(s) :

PCR, Taq

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About This Item

Code UNSPSC :
41106300
Nomenclature NACRES :
NA.54

Durée de conservation

≤18 mo.

Niveau de qualité

Caractéristiques

dNTPs included: no
hotstart: no

Conditionnement

pkg of 250 U (KK1014)
pkg of 2500 U (BK1000)
pkg of 500 U (KK1015)
pkg of 5000 U (BK1002)

Fabricant/nom de marque

Roche

Technique(s)

PCR: suitable

Entrée

purified DNA

Température de stockage

−20°C

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Application

KAPA Taq PCR Kit has been used in:
  • High throughput PCR
  • Amplification of low copy DNA templates
  • Multiplex PCR
  • Specific amplification of complex templates
  • RT-PCR
  • random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR)
  • Polymerase chain reaction (PCR)
  • Genotyping

Actions biochimiques/physiologiques

KAPA Taq PCR Kit, which contains 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 hot start 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.

Caractéristiques et avantages

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 DNA Polymerase can replace any commercial Taq DNA polymerase in an existing protocol.
  • The final MgCl2 concentration may need to be optimized to account for differences in buffer formulation.
  • KAPA Taq Buffers contain MgCl2 at a final concentration of 1.5 mM. Buffer A is recommended as first approach and for applications requiring high yields. Buffer B is recommended for applications where high sensitivity is required (e.g. when the template is limiting). Both buffers may be evaluated to determine the buffer most suitable for a specific application.
  • 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.

Qualité

Each batch of KAPA Taq DNA Polymerase is confirmed to contain <2% contaminating protein (Agilent Protein 230Assay). KAPA Taq Ready Mixes 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.

Notes préparatoires

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

Autres remarques

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

Informations légales

HOTSTART is a registered trademark of Molecular BioProducts, Inc.

Composants de kit seuls

Réf. du produit
Description

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

  • 10X KAPA Taq Buffer A

  • 10X KAPA Taq Buffer B

  • MgCl2 25 mM

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Improvement of poly-[gamma]-glutamic acid (PGA) producing Bacillus subtilis SBMYP-1 by N-methyl-N′-nitro-N-nitrosoguanidine (NTG) mutagenesis.
Mahidsanan T and Gasaluck P
International food research journal., 23(2), 751-751 (2016)
Direct conversion of mouse embryonic fibroblasts into functional keratinocytes through transient expression of pluripotency-related genes.
Iacovides D, et al.
Stem Cell Research & Therapy, 7(1), 98-98 (2016)
SNES: single nucleus exome sequencing
Marco L Leung
Genome Biology, 16(55) (2015)
Demetris Iacovides et al.
Data in brief, 20, 1602-1606 (2018-09-29)
We have performed whole transcriptome sequencing of 5-FU resistant and 5-FU sensitive tumors generated in a mouse model of de novo carcinogenesis that closely recapitulates tumor initiation, progression and maintenance in vivo. Tumors were generated using the DMBA/TPA model of
Charalambos Loizides et al.
PloS one, 10(12), e0143840-e0143840 (2015-12-10)
Tumorigenesis is a complex, multistep process that depends on numerous alterations within the cell and contribution from the surrounding stroma. The ability to model macroscopic tumor evolution with high fidelity may contribute to better predictive tools for designing tumor therapy

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