Przejdź do zawartości
Merck
Wszystkie zdjęcia(2)

Kluczowe dokumenty

TAQKB

Roche

KAPA Taq PCR Kit

Synonim(y):

PCR, Taq

Zaloguj sięWyświetlanie cen organizacyjnych i kontraktowych


About This Item

Kod UNSPSC:
41106300
NACRES:
NA.54

okres trwałości

≤18 mo.

Poziom jakości

Właściwości

dNTPs included: no
hotstart: no

opakowanie

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

producent / nazwa handlowa

Roche

metody

PCR: suitable

moc wejściowa

purified DNA

temp. przechowywania

−20°C

Szukasz podobnych produktów? Odwiedź Przewodnik dotyczący porównywania produktów

Zastosowanie

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

Działania biochem./fizjol.

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.

Cechy i korzyści

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.

Jakość

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.

Uwaga dotycząca przygotowania

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.

Inne uwagi

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

Informacje prawne

HOTSTART is a registered trademark of Molecular BioProducts, Inc.
Ta strona może zawierać tekst przetłumaczony maszynowo.

Tylko elementy zestawu

Numer produktu
Opis

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

  • 10X KAPA Taq Buffer A

  • 10X KAPA Taq Buffer B

  • MgCl2 25 mM

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

does not flash

Temperatura zapłonu (°C)

does not flash


Wybierz jedną z najnowszych wersji:

Certyfikaty analizy (CoA)

Lot/Batch Number

Nie widzisz odpowiedniej wersji?

Jeśli potrzebujesz konkretnej wersji, możesz wyszukać konkretny certyfikat według numeru partii lub serii.

Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Klienci oglądali również te produkty

SNES: single nucleus exome sequencing
Marco L Leung
Genome Biology, 16(55) (2015)
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)
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)
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

Produkty

An overview of directed evolution and the methods for generating proteins with optimized or entirely new functions.

Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.

Skontaktuj się z zespołem ds. pomocy technicznej