AmpliTaq™ DNA Polymerase with Buffer I or Buffer II

Zitierungen und Referenzen (1798)

Applied Biosystems™

AmpliTaq™ DNA Polymerase with Buffer I or Buffer II

Name: AmpliTaq™ DNA Polymerase with Buffer I or Buffer II
SKU: N8080160
Price: 270.00 EUR

AmpliTaq DNA-Polymerase ist eine 94 kDa große, thermostabile, rekombinante DNA-Polymerase, die durch Expression einer modifizierten Form des Thermus aquaticus (Taq)-DNA-Polymerase-GensWeitere Informationen

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Katalognummer	Enthält	Menge
N8080160	Buffer I	250 Einheiten
N8080161	Buffer II	250 Einheiten
N8080172	Buffer II	1.000 Einheiten
N8080153	Buffer II	3000 Einheiten
N8080156	Buffer II	5000 Einheiten
N8080186	Buffer II	25.000 Einheiten
N8080152	Buffer I	3000 Einheiten
N8080155	Buffer I	5000 Einheiten
N8080171	Buffer I	1000 Einheiten
N8080185	Buffer I	25000 Einheiten

10 Optionen

Katalognummer N8080160

Preis (EUR)

270,00

Each

Zum Warenkorb hinzufügen

Enthält:

Buffer I

Menge:

250 Einheiten

Großbestellung oder individuelle Größe anfordern

Preis (EUR)

270,00

Each

Zum Warenkorb hinzufügen

AmpliTaq DNA-Polymerase ist eine 94 kDa große, thermostabile, rekombinante DNA-Polymerase, die durch Expression einer modifizierten Form des Thermus aquaticus (Taq)-DNA-Polymerase-Gens in E. coli gewonnen wird. Eines der spezifischsten für die PCR verfügbaren Enzyme, dessen rekombinante Eigenschaften sowie seine Reinigungsmethode für unvergleichliche, fläschchen- sowie chargenübergreifende Reinheit und Reproduzierbarkeit sorgen.

Merkmale dieses Enzyms:

Die AmpliTaq DNA-Polymerase ist eines der am besten beschriebenen, für die PCR verfügbaren Enzyme, was ihren allgemeine Nutzen und ihre Effektivität bezeugt

Dank thermischem Aktivitätsprofil eine optimale Wahl für PCR-Anwendungen

QC-getestet, um reproduzierbare Ergebnisse zu gewährleisten

Zuverlässige und robuste PCR
Das thermische Aktivitätsprofil von AmpliTaq DNA-Polymerase eignet sich gut für PCR-Anwendungen, da seine optimale Aktivität in demselben Bereich liegt, in dem das Annealing von Primern auftritt (55 – 75 °C). Die Halbwertszeit des Enzyms beträgt ∼40 Minuten bei 95 °C und bietet so eine Thermostabilität, die den Anforderungen der schwierigsten PCR-Anwendungen entspricht. Diese AmpliTaq DNA-Polymerase wird mit GeneAmp 10X PCR-Puffer II und MgCl₂-Lösung geliefert.

Für eine hervorragende PCR-Leistung empfehlen wir die DreamTaq DNA-Polymerase.

Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.

Specifications

Exonukleaseaktivität5' – 3'

Wiedergabetreue (vs. Taq)1X

FormatEigenständiges Enzym

Hot-StartNein

EnthältBuffer I

Anzahl Reaktionen200 Reaktionen

Überhang3'-A

PolymeraseAmpliTaq DNA-Polymerase

ProdukttypDNA-Polymerase

Menge250 Einheiten

ReaktionsformatSeparate Komponenten

VersandbedingungTrockeneis

Größe (Endprodukt)5 kb oder weniger

AusgangsmaterialDNA

Konzentration5 E/μl, 10X

Zur Verwendung mit (Anwendung)Standard-PCR

ReaktionsgeschwindigkeitStandard

Unit SizeEach

Inhalt und Lagerung

Inhalt:

50 μl AmpliTaq™ DNA-Polymerase (5 E/μl)
1,5 ml GeneAmp™ 10X-PCR-Puffer I (100 mM Tris-HCl, pH 8,3, 500 mM KCl, 15 mM MgCl2, 0,01 % (w/v) Gelatine).

Lagerung bei -20 °C.

Häufig gestellte Fragen (FAQ)

My oligonucleotide does not appear to be the right length when I checked by gel electrophoresis. Why is this?

Oligos should be run on a polyacrylamide gel containing 7 M urea and loaded with a 50% formamide solution to avoid compressions and secondary structures. Oligos of the same length and different compositions can electrophorese differently. dC's migrate fastest, followed by dA's, dT's, and then dG's. Oligos containing N's tend to run as a blurry band and generally have a problem with secondary structure.

The primers I am using worked for PCR initially, but over time, have stopped working. What happened?

Primers should be aliquoted for single use before PCR set-up. Heat just the aliquoted primers to 94 degrees for 1 min. Quick chill the primer on ice before adding to the PCR reaction. Some primers may anneal to themselves or curl up on themselves.

I don't see a pellet in my oligo tube order. Should I ask for a replacement?

The drying method dries the primer in a thin layer along the sidewalls of the tube instead of the bottom, therefore a pellet is not always visible and should still be ready to use.

There is a ball-shaped pellet at the bottom of my oligo tube. What is this and can I still use my oligo?

If the oligo was overheated, it will appear as a “ball”-shaped pellet attached to the bottom of the tube. This should not affect the quality of the oligo, and the oligo should be readily soluble in water.

There is a green color in my lyophilized oligo. Can I still use it?

If an oligo appears green in color, this is most likely due to ink falling into the tube. The oligo should still be fully functional. The color can be removed by doing an ethanol precipitation.

View all AmpliTaq™ DNA Polymerase with Buffer I or Buffer II FAQs

Zitierungen und Referenzen (1798)

Zitierungen und Referenzen

Abstract

Chimpanzee Fab fragments and a derived humanized immunoglobulin G1 antibody that efficiently cross-neutralize dengue type 1 and type 2 viruses.

Authors:Goncalvez AP; Men R; Wernly C; Purcell RH; Lai CJ

Journal:Journal of Virology

PubMed ID:

Passive immunization with monoclonal antibodies from humans or nonhuman primates represents an attractive alternative to vaccines for prevention of illness caused by dengue viruses (DENV) and other flaviviruses, including the West Nile virus. In a previous study, repertoire cloning to recover Fab fragments from bone marrow mRNA of chimpanzees infected ... More

Molecular genetics of tetrahydrobiopterin (BH4) deficiency in the Maltese population.

Authors:Farrugia R; Scerri CA; Montalto SA; Parascandolo R; Neville BG; Felice AE

Journal:Molecular Genetics and Metabolism

PubMed ID:

Deficient activity of the Dihydropteridine Reductase enzyme (DHPR; EC 1.5.1.34; OMIM 261630) is due to mutations in the Quinoid Dihydropteridine Reductase gene on 4p15.3 (QDPR; RefSeq NM_000320). It results in defective recycling of tetrahydrobiopterin (BH(4)) and homozygotes have a rare form of atypical Hyperphenylalaninaemia and Phenylketonuria (aPKU). The heterozygote frequency ... More

A specific structural requirement for ergosterol in long-chain fatty acid synthesis mutants important for maintaining raft domains in yeast.

Authors:Eisenkolb M; Zenzmaier C; Leitner E; Schneiter R

Journal:Molecular Biology of the Cell

PubMed ID:

Fungal sphingolipids contain ceramide with a very-long-chain fatty acid (C26). To investigate the physiological significance of the C26-substitution on this lipid, we performed a screen for mutants that are synthetically lethal with ELO3. Elo3p is a component of the ER-associated fatty acid elongase and is required for the final elongation ... More

Procollagen with skipping of alpha 1(I) exon 41 has lower binding affinity for alpha 1(I) C-telopeptide, impaired in vitro fibrillogenesis, and altered fibril morphology.

Authors:Cabral WA; Fertala A; Green LK; Korkko J; Forlino A; Marini JC

Journal:The Journal of Biological Chemistry

PubMed ID:

Previous in vitro data on type I collagen self-assembly into fibrils suggested that the amino acid 776-796 region of the alpha1(I) chain is crucial for fibril formation because it serves as the recognition site for the telopeptide of a docking collagen monomer. We used a natural collagen mutation with a ... More

Vibrio fischeri LuxS and AinS: comparative study of two signal synthases.

Authors:Lupp C; Ruby EG

Journal:Journal of Bacteriology

PubMed ID:

Vibrio fischeri possesses two acyl-homoserine lactone quorum-sensing systems, ain and lux, both of which are involved in the regulation of luminescence gene expression and are required for persistent colonization of the squid host, Euprymna scolopes. We have previously demonstrated that the ain system induces luminescence at cell densities that precede ... More

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