mTaq DNA Polymerase - EnzymoPure™

Cat. No.: M665697
Zu bestellen verfügbar
QUALITÄT & REINHEIT EnzymoPure™ ? EnzymoPure™ — Aladdin's line of high-quality enzymatic solutions. Use when enzyme purity and defined activity drive assay or process performance.
Storage
Store at -20°C,Avoid repeated freezing and thawing
Shipped In
Ice chest + Ice pads
★
Größe
Deutschland (EU)
USA*
Preis
Menge
500U
M665697-500U
Auf Bestellung · 8–12 Wochen
520,56€
2500U
M665697-2500U
Auf Bestellung · 8–12 Wochen
1.859,48€
Enter a quantity for the sizes you want to add.
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Warum diese Qualität

EnzymoPure™ EnzymoPure™ für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Store at -20°C,Avoid repeated freezing and thawing Versand Ice chest + Ice pads. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 0 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

MTaq DNA Polymerase is a novel DNA polymerase obtained by deletion of a segment of amino acid at the N-terminus of Taq DNA Polymerase and mutation modification. Through modification, this product can produce tolerance to inhibitors present in whole blood, allowing for direct amplification of DNA in human and mouse whole blood samples without the need for prior genome extraction and purification. The 3 'end of the PCR product is A and can be directly used for T/A cloning.

M665697

Component

500 U

2500 U

Storage

M665697A

mTaq DNA Polymerase, 5 U/μL

100 μL

5×100 μL

-20℃.Avoid freeze/thaw cycle. 

M665697B

mTaq PCR Buffer, 10×

1.8 mL

5×1.8 mL

-20℃.Avoid freeze/thaw cycle. 

Notice: mTaq PCR Buffer contains 30 mM MgCl₂

Quality control:
After multiple column purifications, SDS-PAGE detected a purity of over 99%; No exogenous nuclease activity detected; PCR method for detecting residual DNA without host; Can effectively amplify single copy genes in the human genome; Store at room temperature for one week without significant changes in activity.
Usage:
1. Before use, please invert the mTaq DNA Polymerase repeatedly until completely mixed.
2. Place the PCR thin-walled tube on ice and add the following reagents except for whole blood.

Reagent 50 μlReaction system Final concentration
mTaq DNA Polymerase 1 μl /
mTaq PCR Buffer, 10× 5 μl 1×
dNTP Mix,2.5 mM each 4 μl 200 μM each
Forward Primer (10 µM) 2 μl 0.4 μM
Reverse Primer (10 µM) 2 μl 0.4 μM
Whole blood* ≤10% /
RNase-Free water x μl /
Total 50 μl /

Attention: 

1) Before adding whole blood, repeatedly aspirate and beat up and down to completely mix various reagents
2) DNA template: Whole blood can be treated with sodium heparin, Na EDTA, K-EDTA, or sodium citrate. It is usually recommended to have a whole blood content of 5-10%. It is not recommended to use high concentration blood. For templates with high GC content, add 10% DMSO.
3) Primers: Oligonucleotide primers typically contain 20-30 nucleotides in length, with a GC content of 40-60% and evenly distributed within the primers. In conventional PCR reactions, the primer concentration should be at the final concentration of 0.1-1.0 μ M serves as a reference for setting the range.
3. Finally, add whole blood to the bottom of the tube.
4. PCR reaction conditions

Step Temperature Time /
Pre denaturation 95℃ 5 min /
Denaturation 95℃ 30 s 35-40 cycles
Anneal 50-68℃ 30 s 35-40 cycles
Extend 72℃ 250-500 bp/min 35-40 cycles
Finally extended 72℃ 10 min /


Attention:
1) Preheat the PCR instrument at 94-95 ℃ and place the sample on the PCR instrument to start cycling.
2) MTaq enhances cold sensitivity and has some hot start characteristics. Usually, the production of non-specific products can be avoided by preparing reaction ingredients on ice, adding polymerase, and preheating the thermal cycler to denaturation temperature (95 ℃) for immediate reaction.
3) Denaturation temperature and time: In order to fully lyse blood cells and release/denature DNA before the PCR cycle, an initial denaturation temperature of 95 ℃ for 5 minutes is required.
4) Annealing temperature and time: The annealing time is usually 30 seconds to 1 minute. The annealing temperature can be lower than the theoretical annealing temperature (Tm) by starting at 5 ℃ and optimizing through gradient PCR.
5) Extension time: The extension reaction is usually carried out at 72 ℃. Generally, the extension time is 1 minute every 250-500 bp. Recommend final extension at 72 ℃ for 10 minutes.
6) Typically, 35-40 cycles can achieve optimal amplification.
5. Result detection: After the reaction is completed, take 5 µ l of the reaction product and add it to the electrophoresis buffer for electrophoresis detection.

Spezifikationen

Spezifikationen & Reinheit
EnzymoPure™
Storage
Store at -20°C,Avoid repeated freezing and thawing
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Note
EnzymoPure™
Product Line
Biologische Produkte

Dokumentation

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