Przejdź do zawartości
Merck

D9307

Sigma-Aldrich

JumpStart Taq DNA Polymerase

with MgCl2

Synonim(y):

gorący start PCR, polimeraza DNA gorącego startu

Zaloguj sięWyświetlanie cen organizacyjnych i kontraktowych


About This Item

Numer MDL:
Kod UNSPSC:
12352204
NACRES:
NA.55

Formularz

liquid

zastosowanie

sufficient for 1500 reactions
sufficient for 250 reactions
sufficient for 50 reactions

Właściwości

dNTPs included: no
hotstart

stężenie

2.5 units/μL

metody

PCR: suitable

kolor

colorless

moc wejściowa

purified DNA

przydatność

suitable for PCR

Zastosowanie

agriculture

Warunki transportu

wet ice

temp. przechowywania

−20°C

Szukasz podobnych produktów? Odwiedź Przewodnik dotyczący porównywania produktów

Opis ogólny

JumpStart Taq DNA polymerase is a combination of Sigma′s high-performance Taq DNA Polymerase and JumpStart Taq antibody. The Taq DNA Polymerase activity is inactivated by combining the enzyme with JumpStart Taq antibody, a neutralizing monoclonal antibody to Taq DNA polymerase. Antibody inactivation provides a simple, efficient procedure for hot-start PCR. During PCR, JumpStart Taq DNA polymerase is inactive at low (room) temperature, as the temperature is raised above 70 °C in the first denaturation step of the cycling process, the complex dissociates, and the polymerase becomes fully active.

Zastosowanie

  • For PCR amplifications that require reduced non-specific amplification
  • For multiplex PCR
  • For reduction of primer dimers
JumpStart Taq DNA Polymerase has been used:
  • in the amplification of DNA libraries of varying sizes
  • in a methylation-specific, quantitative real-time polymerase chain reaction (MS-qPCR) to determine the BRCA1 promoter methylation status
  • in the generation of plasmid by amplifying the full-length of HIF1β via PCR

Cechy i korzyści

  • Reduces non-specific amplification
  • Increases PCR specificity and yield
  • Reduces set-up time concerns associated with manual or wax Hot Start methods
  • Activation time of less than 1 minute

Opakowanie

JumpStart Taq DNA Polymerase is provided with a 10× reaction buffer available with and without MgCl2. The magnesium free 10× buffer also includes a separate tube of 25 mM MgCl2 for optimization.
Supplied with 10× reaction buffer containing 15 mM MgCl2

Inne uwagi

Sigma′s JumpStart Taq DNA Polymerase is an antibody-inactivated hot-start enzyme designed to minimize non-specific amplification while increasing target yield. Once the reaction temperature reaches 70°C, Taq DNA polymerase activity is restored and the resulting PCR exhibits a higher specificity and yield. This antibody-enzyme complex allows for easy and convenient set-up with less contamination risk than manual hot-start techniques. The enzyme may also be included in the master mix preparation resulting in more consistency from one reaction to the next.
View more detailed information on JumpStart Taq enzymes at www.sigma-aldrich.com/hotstart.

Definicja jednostki

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

Informacje prawne

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.

Antibody licensed for in vitro research use under U.S. Patent No. 5,338,671 and 5,587,287, and corresponding patents in other countries.
JumpStart is a trademark of Sigma-Aldrich Co. LLC
Ta strona może zawierać tekst przetłumaczony maszynowo.

Kod klasy składowania

10 - Combustible liquids

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


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

High quality bisulfite sequencing using nanogram amounts of genomic DNA
Sun J, et al.
International journal of biochemistry and biotechnology, 2, 449-456 (2013)
Ning Li et al.
Methods (San Diego, Calif.), 52(3), 203-212 (2010-05-01)
There are numerous approaches to decipher a whole genome DNA methylation profile ("methylome"), each varying in cost, throughput and resolution. The gold standard of these methods, whole genome bisulfite-sequencing (BS-seq), involves treatment of DNA with sodium bisulfite combined with subsequent
Memory T Cells Expressing an NKG2D-CAR Efficiently Target Osteosarcoma Cells.
Lucía Fernández et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 23(19), 5824-5835 (2017-07-01)
Whole genome DNA methylation analysis based on high throughput sequencing technology
Li N, et al.
Methods, 52(3), 203-212 (2010)
Disruption of Abi1/Hssh3bp1 expression induces prostatic intraepithelial neoplasia in the conditional Abi1/Hssh3bp1 KO mice
Xiong X, et al.
Oncogenesis, 1(9), e26-e26 (2012)

Protokoły

This protocol provides a simple and convenient method to isolate, amplify and purify genomic DNA from saliva

Mycoplasma contamination of cell cultures is a serious issue impacting cell model validity. PCR testing for mycoplasma is an inexpensive, sensitive, and specific method for detecting contamination.

Blood cards provide the convenience of archiving small volumes of blood. However, many times genomic DNA from these samples is limited, This protocol provides a simple and convenient method to extract genomic DNA from a blood card. Once the DNA has been extracted, it can then be amplified using the amplification protocol

Zanieczyszczenie hodowli komórkowych mykoplazmą jest poważnym problemem wpływającym na wiarygodność modeli komórkowych. Test PCR na obecność mykoplazmy jest niedrogą, czułą i specyficzną metodą wykrywania skażenia.

Zobacz wszystko

Powiązane treści

GenomePlex® Whole Genome Amplification is the method of extracting DNA from the animal sample. GenomePlex® products have been used to amplify genomic DNA from chicken, porcine, bovine, fish, and shrimp source.

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