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Merck

D1806

Sigma-Aldrich

Taq DNA Polymerase from Thermus aquaticus

with 10× PCR reaction buffer containing MgCl2

Szinonimák:

MgCl2 taq polymerase, Taq polymerase

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

CAS-szám:
Enzyme Commission szám:
MDL-szám:
UNSPSC kód:
12352204
NACRES:
NA.55

biológiai forrás

enzyme from bacterial (Thermus Aquaticus)

Minőségi szint

rekombináns

expressed in E. coli

Forma

liquid

használat

sufficient for 10000 reactions
sufficient for 3000 reactions
sufficient for 500 reactions

molekulatömeg

94 kDa

Jellemzők

dNTPs included: no
hotstart: no

koncentráció

5 units/μL

technika/technikák

PCR: suitable

szín

colorless

bemenet

purified DNA

alkalmasság

suitable for PCR and automated sequencing reactions

alkalmazás(ok)

agriculture

kiszállítva

wet ice

tárolási hőmérséklet

−20°C

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Általános leírás

Taq DNA Polymerase is a thermostable enzyme derived from the thermophilic bacterium Thermus aquaticus. The enzyme is in a recombinant form, expressed in E. coli. It can withstand repeated heating to 95 °C without significant loss of activity. Each lot of Taq DNA Polymerase is tested for PCR amplification and double-stranded sequencing.

Alkalmazás

Taq DNA Polymerase from Thermus aquaticus has been used:
  • in the quantification of fungal growth by polymerase chain reaction (PCR) and photometric assay
  • in conventional reverse transcriptase (RT)-PCR
  • in simple sequence repeats (SSR) genotyping
  • as a component of PCR mix for amplification of genomic and mitochondrial DNA
  • in direct tetra-primer amplification refractory mutation system (T-ARMS) PCR to amplify dried whole blood samples

Biokémiai/fiziológiai hatások

Taq polymerase catalyzes oligonucleotide primer-driven, DNA template dependent incorporation of dNTPs into complimentary DNA strands. It displays both 5′ to 3′ polymerase and exonuclease activities.

Tulajdonságok és előnyök

  • Low per unit cost of Taq

Kiszerelés

Taq DNA Polymerase with 10× reaction buffer containing MgCl2
Taq DNA polymerase comes with the choice of an optimized 10× reaction buffer including MgCl2 (D1806) or a 10× reaction buffer without MgCl2 plus a separate tube of MgCl2 for titration (D4545). The latter option may be necessary to determine optimal conditions for amplification.

Egyéb megjegyzések

Taq DNA Polymerase is a specialized thermostable enzyme isolated from the thermophilic bacterium Thermus aquaticus. The recombinant form of this enzyme is expressed in E. coli. This 94 kDa protein shows no detectable levels of contaminating endonucleases or exonucleases by SDS-PAGE. It has both 5′→3′ polymerase and exonuclease activity.

Egység definíció

One unit will incorporate 10 nmol of total dNTPs into acid-precipitable DNA in 30 min at 74 °C.

Jogi információk

Use of this product is covered by one or more of the following US patents and corresponding patent claims outside the US: US 8,404,464 and US 7,972,828. The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims.

Tárolási osztály kódja

12 - Non Combustible Liquids


Válasszon a legfrissebb verziók közül:

Analitikai tanúsítványok (COA)

Lot/Batch Number

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Dokumentumtár megtekintése

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Determination of Polymorphisms in the GDF5 and EPS8 Genes by HRM Analysis in Holstein Cattle
Sonmez Z, et al.
Pakistan Journal of Zoology (2021)
Human endogenous retrovirus family HERV-K (HML-2) RNA transcripts are selectively packaged into retroviral particles produced by the human germ cell tumor line Tera-1 and originate mainly from a provirus on chromosome 22q11. 21
Ruprecht K, et al.
Journal of Virology, 82(20), 10008-10016 (2008)
Fundamental study on the influence of Fusarium infection on quality and ultrastructure of barley malt
Oliveira P M, et al.
International Journal of Food Microbiology, 156(1), 32-43 (2012)

Cikkek

Explore PCR's history, from discovery to Nobel Prize. Discover real-time PCR (qPCR) and digital PCR developments.

Protocols

Hot Start dNTPs block DNA polymerase until heat activation, enhancing PCR specificity.

Learn standard PCR protocol steps and review reagent lists or cycling parameters. This method for routine PCR amplification of DNA uses standard Taq DNA polymerase.

Tudóscsoportunk valamennyi kutatási területen rendelkezik tapasztalattal, beleértve az élettudományt, az anyagtudományt, a kémiai szintézist, a kromatográfiát, az analitikát és még sok más területet.

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