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Terminal Transferase Buffer Pack (3 x 500microl)

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M1893

Description

Terminal Deoxynucleotidyl Transferase, Recombinant, catalyzes the repetitive addition of mononucleotides to the terminal 3´-OH of a DNA initiator accompanied by the release of inorganic phosphate. Single-stranded DNA is preferred as an initiator. Polymerization is not template-dependent. The addition of 1mM Co2+ (as CoCl2) in the reaction buffer allows the tailing of 3´-ends with varying degrees of efficiency.

Features - Benefits

  • Tails Any Type of 3´ End: The presence of 1mM CoCl2 in the reaction buffer allows the tailing of any type of 3´ end (3´ and 5´ overhangs or blunt ends).
  • Tested for Apoptotic DNA Labeling: Each lot of enzyme is qualified for success in the procedure outlined in the DeadEnd™ Fluorometric TUNEL System Technical Bulletin #TB235.
  • Provided with 5X Reaction Buffer: 500mM cacodylate buffer (pH 6.8 at 25°C), 5mM CoCl2, 0.5mM DTT.
  • Choose Your Configuration: Learn more about our custom options for this product at: www.promega.com/custom/

Applications

  • Tailing reactions to add complementary homopolymer tails to DNA vectors and cDNA.
  • 3´ end-labeling.
  • TUNEL assays.

For more information, see the Protocols & Applications Guide.

Specifications

QC Tests

Activity, endonuclease, DNase, RNase, 3´ end-labeling, apoptotic DNA end-labeling.

Source

Recombinant E. coli strain.

Storage Buffer

50mM potassium phosphate (pH 6.4), 100mM NaCl, 1mM β-mercaptoethanol, 0.1% Tween® 20 and 50% glycerol.

Storage Conditions

Store at –20°C.

Unit Definition

One unit of activity catalyzes the transfer of 0.5 picomoles of ddATP to oligo(dT)16 per minute at 37°C in 1X Terminal Transferase Buffer. The resulting oligo(dT)17 is measured by HPLC.

For product intended use please see Patents & Disclaimers tab.

Resources

Use Restrictions

M1871, M1875, M1893 For Research Use Only. Not for Use in Diagnostic Procedures.

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