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tech@sbsbio.com
Beijing SBS Genetech Co.,Ltd.
Beijing SBS Genetech Co.,Ltd.
broken image

from China, for the World

for Superior Biology Services since 2000

  • Home
  • Product 
    • All Products
    • Custom Services
    • Catalog Products
    • Innovative Systems
    • Nucleic Acid Related
    • Natural Compounds
    • Synthetic Biology
    • Enzymes
  • POCT Solution 
    • LAMP
    • RPA
    • CRISPR
    • DNA-Free Enzymes
    • Freeze-Drying System
    • Lateral Flow System
  • About 
    • About SBS
    • Achievements
    • Ecosystem
    • Legal Statement
  • Contact
  • …  
    • Home
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      • All Products
      • Custom Services
      • Catalog Products
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      • Nucleic Acid Related
      • Natural Compounds
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    • POCT Solution 
      • LAMP
      • RPA
      • CRISPR
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      • Freeze-Drying System
      • Lateral Flow System
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Terminal Transferase (20 U/μl)

Terminal Transferase (20 U/μl)

$135.00 - $500.00
Terminal transferase (TdT) is a template-independent DNA polymerase that catalyzes the binding of deoxynucleotides to the 3' hydroxyl end of DNA molecules. Single-stranded and double-stranded DNA molecules with either sticky or blunt ends can all serve as substrates for TdT, with tailing lengths ranging from 5 to 300 nt.
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All products have special prices for bulk purchase, please contact for more details if required.

 

Cat. No.: TT-500 (for 500U)

Cat. No.: TT-2500 (for 2,500U)

 

Description

This terminal transferase (TdT) has a molecular weight of 58.3 kDa and no 5' and 3' exonuclease activities. The addition of Co2+ to the reaction can improve the tailing efficiency. The enzyme is widely used in DNA 3' end addition homopolymer, DNA 3' end labeling using modified bases (such as ddNTP, DIG-dUTP), TdT-mediated dUTP nick end labeling technology (in situ detection of apoptosis), and other tests. The enzyme is tested free of DNA endonuclease and exonuclease contamination and RNase.

 

Application

  • Oligonucleotide or DNA 3' hydroxyl end labeling
  • DNA tailing
  • 5'-RACE
  • Synthesis of oligomeric strands of the same deoxynucleotide
 

Unit Definition

The amount of enzyme required to catalyze the addition of 1 nmol dNTP to the 3' hydroxyl end of a polynucleotide within 60 min at 37°C is defined as an active unit.

 

1 x TdT Buffer

100 mM KCl, 30 mM Tris-acera, 0.05% (v/v) Triton X-100 (pH 7.5 at 25°C)

 

Storage

Stored at -20°C for 3 years.

 

Thermal inactivation

75°C for 20 min.

 

Notes

  • The activity of Terminal Transferase can be lost by an appropriate amount of EDTA.
  • Metal ion chelators, higher concentrations of ammonium ions, chloride ions, iodine ions, and phosphate ions all have inhibitory effects on Terminal Transferase activity.
 
 
Only for research and not intended for treatment of humans or animals
 
 

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SBS Genetech is a long-term sponsor of Cold Spring Harbor Laboratory

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