• Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011
  • Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011
  • Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011
  • Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011
  • Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011
  • Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011
  • Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011
Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011

Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011

Product Details:

Place of Origin: China
Brand Name: GDSBio
Certification: /
Model Number: P1011

Payment & Shipping Terms:

Minimum Order Quantity: 1Bag
Packaging Details: small package or bulk distribute or OEM
Delivery Time: 8 work days
Payment Terms: L/C, D/A, D/P, T/T, Western Union, MoneyGram
Supply Ability: 100 Bag/Bags Per Day
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Detail Information

Cat. No.: P1011 Concentration: 5U/μl
Appearance: Blue Buffer Group: PCR Master Mix
Activity: Pass Amplification Capability: Good
Logo Printing: With Logo Printing Transport Package: Packing
Production Capacity: 100 Bag/Bags Per Day Storage Conditions: Store At -20°C
High Light:

5U/μl Taq DNA Polymerase

,

Taq DNA Polymerase 100 μl

Product Description

 

Taq DNA Polymerase

#P1011, 500U

 

Concentration: 5U/μl

Contents:

Taq DNA Polymerase 100 μl
10× PCR Buffer (Mg2+ Free) 1.25 ml
6× Loading Buffer 1 ml
25mM MgCl2 1.25 ml

 

Store at -20°C

For research use only.

In total 4 vials.

 

Description

Taq DNA Polymerase is a thermostable recombinant DNA polymerase derived from thermophilic bacterium Thermus aquaticus. Its molecular weight is 94 kDa. Taq DNA Polymerase can amplify DNA target up to 5 kb (simple template). The elongation velocity is 2kb/min (70~75°C). It has 5' to 3' polymerase activity but lacks of 3' to 5' exonuclease activity that results in a 3'-dA overhangs PCR product.

Unit Definition

One unit is defined as the amount of the enzyme required to catalyze the incorporation of 10 nmole of dNTPs into an acid-insoluble form in 30 minutes at 70°C using hering sperm DNA as substrate.

Storage Buffer

20mM Tris-HCl (pH 8.0), 100mM KCl, 3.2mM MgCl2, 1mM DTT, 0.1% Triton X-100, 0.1% Tween20, 0.2mg/ml BSA, 50% (V/V) glycerol.

10× PCR Buffer without Mg2+

100mM Tris-HCl (pH 8.8), 500mM KCl, 1% Triton X-100.

Applications

• PCR amplification of DNA fragments as long as 5 kb

• DNA labeling

• DNA sequencing

• PCR for cloning

Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011 0

GDSBio has a complete product line. With PCR technology as the core, focusing on molecular biology techniques such as ordinary PCR, fluorescence quantitative PCR, NGS library preparation, nucleic acid electrophoresis, nucleic acid purification, etc.It has developed reagents for molecular biology research and diagnosis, and completed the layout of the whole industrial chain from molecular biology reagents, medical lab supplies to specialized services.

Taq DNA Polymerase PCR Amplification Of DNA Fragmentsr P1011 1

Product operation manual:P1011(mg2+free)Taq DNA Polymerase V1.2.pdf

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