4521371

Thermo Scientific™ T4 DNA Ligase (5 U/μL)

T4 DNA Ligase catalyzes the formation of a phosphodiester bond between juxtaposed 5'-phosphate and 3'-hydroxyl termini in duplex DNA or RNA.

Manufacturer: Fischer Scientific

The price for this product is unavailable. Please request a quote

Concentration

5 U/μL

Enzyme

DNA Ligase

Compatible Buffer

10X T4 DNA Ligase Buffer

Product Type

T4 DNA Ligase

Related Products

Img

Fischer Scientific

FEREL0011

--

Img

Fischer Scientific

FEREL0014

--

Img

Fischer Scientific

FEREL0012

--

Img

Thermo Scientific™

FEREL0016

--

Img

Thermo Scientific™

FEREL0013

--

Img

Thermo Scientific™

FEREL0021

--

Img

Fischer Scientific

4918234

Ideal for cloning (blunt-end or coh...

Img

Thermo Scientific™

FEREN0521

--

Description

  • Catalyze the formation of a phosphodiester bond between juxtaposed 5'-phosphate and 3'-hydroxyl termini in duplex DNA or RNA with the Thermo Scientific™ T4 DNA Ligase
  • The enzyme repairs single-strand nicks in duplex DNA, RNA, or DNA/RNA hybrids
  • It also joins DNA fragments with either cohesive or blunt termini, but has no activity on single-stranded nucleic acids
  • The T4 DNA Ligase requires ATP as a cofactor
  • Highlights Active in Themo Scientific restriction enzyme, PCR, and RT buffers (when supplemented with ATP) Fast – sticky-end ligation is completed in 10 minutes at room temperature Supplied with PEG solution for efficient blunt-end ligation Applications Cloning of restriction enzyme generated DNA fragments Cloning of PCR products Joining of double-stranded oligonucleotide linkers or adaptors to DNA Site-directed mutagenesis Amplified fragment length polymorphism (AFLP) Ligase-mediated RNA detection ( see Reference 3) Nick repair in duplex DNA, RNA or DNA/RNA hybrids Self-circularization of linear DNA
  • Notes Binding of T4 DNA Ligase to DNA may result in a band shift in agarose gels
  • To avoid this, incubate samples with 6X DNA Loading Dye & SDS Solution at 70°C for 5 min or 65°C for 10 minutes and chill on ice prior to electrophoresis
  • The volume of the ligation reaction mixture should not exceed 10% of the competent cell volume in the transformation process
  • Prior to electro-transformation, remove T4 DNA Ligase from the ligation mixture by spin column or chloroform extraction
  • The extracted DNA can be further precipitated with ethanol.

Compare Similar Items

Show Difference

Img

Fischer Scientific

4521371

T4 DNA Ligase catalyzes the formati...


Concentration:
5 U/μL

Enzyme:
DNA Ligase

Compatible Buffer:
10X T4 DNA Ligase Buffer

Product Type:
T4 DNA Ligase

Img

Fischer Scientific

4521372

T4 Polynucleotide Kinase (T4 PNK) c...


Concentration:
10 U/μL

Enzyme:
T4 Polynucleotide Kinase

Compatible Buffer:
10X Reaction Buffer

Product Type:
T4 Polynucleotide Kinase

Img

Fischer Scientific

4521375

Uracil-DNA Glycosylase (UDG, UNG) c...


Concentration:
1 U/μL

Enzyme:
Uracil-DNA Glycosylase

Compatible Buffer:
10X Reaction Buffer

Product Type:
Uracil DNA Glycosylase

Img

Fischer Scientific

4521378

Ribonuclease H (RNase H) is an endo...


Concentration:
5 U/μL

Enzyme:
RNase

Compatible Buffer:
10X Reaction Buffer

Product Type:
RNase H