Bst DNA Polymerase (large fragment)
For DNA sequencing high GC regions and rapid sequencing from nanogram amounts of DNA templates.
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DNA Polymerase I is a DNA-dependent DNA polymerase. The enzyme catalyzes 5' -> 3' synthesis of DNA and exhibits 3' -> 5’ exonuclease proofreading activity.
Description:
DNA Polymerase I is a mesophilic DNA polymerase that exhibits 5' -> 3' DNA synthesis activity in addition to both 3' -> 5' and 5' -> 3' exonuclease activities. The combination of DNA synthesis and 5' -> 3' nuclease characteristics enable nick-translation during DNA synthesis.
Application:
- Nick translation of DNA to obtain probes with a high specific activity
- Second strand synthesis of cDNA
Source:
A recombinant E. coli strain carrying the PolA gene.
Specific Activity: 6,850U/mg
Supplied in:
25 mM Tris-HCl
0.1 mM EDTA
1.0 mM DTTl
50% Glycerol
pH 7.4 @ 25°C
Supplied with:
10x Blue Buffer
10x Blue Buffer:
500 mM NaCl
100 mM Tris-HCl
100 mM MgCl2
10 mM DTT
pH 7.9 @ 25°C
Unit Definition:
1 unit is defined as the amount of polymerase required to convert 10 nmol of dNTPs into acid insoluble material in 30 minutes at 37°C.
Recommended Storage Condition: -20°C
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For DNA sequencing high GC regions and rapid sequencing from nanogram amounts of DNA templates.
Terminal deoxynucleotidyl transferase (TdT) is a template-independent DNA polymerase that catalyzes the addition of deoxynucleotides to the 3’ hydroxyl terminus of single or double stranded DNA molecules.
addition of deoxynucleotides to the 3′ hydroxyl terminus
origin: E.coli (gen from Z. albicollis)
purity > 95 %
2,500 units, 10,000 U/ml
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