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Taq DNA Polymerase  

Functionally tested and has no detectable contaminating endonucleases or exonucleases

Part # Description Unit Size Your Price(USD)
Qty
71160 50 UN
Taq DNA Polymerase
50units    $20.00
71160 250 UN
Taq DNA Polymerase
250units    $70.00
71160 1000 UN
Taq DNA Polymerase
1000units    $259.00
71160 5000 UN
Taq DNA Polymerase
5000units    $1,170.00
     

Source:

E. coli strain expressing a full length, unmodified clone of Taq DNA Polymerase from Thermus aquaticus(1-3).

Description:
Taq DNA Polymerase is a thermostable enzyme which has a highly processive 5'→3' polymerase activity and a 5'→3' exonuclease activity. USB Taq is functionally tested and has no detectable contaminating endonucleases or exonucleases. Taq DNA Polymerase withstands repeated incubations at 95°C without a significant decrease in enzyme activity, and is suitable for routine PCR. USB Taq DNA Polymerase is supplied with 10X PCR Buffer plus a separate tube of 25mM MgCl2 for optimizing PCR conditions. Each lot is tested for product yield and length in PCR amplification.

View Hi-Res PDF Version
Figure 1. DNA fragments ranging from 1 kb to 6 kb amplified from λ DNA.

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Properties:
Activator: Mg2+

Purity:
Free from detectable non-specific nucleases.

Storage Buffer:
20mM Tris-HCl, pH 8.5, 1mM DTT, 0.1mM EDTA, 100mM KCI, 50% glycerol, stabilizers.

Unit Definition:
One unit incorporates 10 nmol of total nucleotides into acid-insoluble material in 30 min at
74°C in a total volume of 50 μl.

Concentration:
5 units/μl

Assay Conditions:
The reaction mixture (50 μl) contains 25mM TAPS, pH 9.3 (at 25°C), 50mM KCl, 2mM MgCl2, 1mM 2-mercaptoethanol, 200μM dNTPs, 250 μg/ml activated salmon sperm DNA and Taq DNA Polymerase. After incubation at 74°C for 10 min, acid insoluble material is determined.

Tested User Friendly Functional Test:
Tested in a standard PCR.

Functionally Tested 10X PCR Reaction Buffer (included, PN 71165):
100mM Tris-HCl (pH 8.6), 500mM KCl, 15mM MgCl2

Functionally Tested MgCl2 (included, PN 71167):
25mM solution

References:

  1. INNIS, M. A., MYAMBO, K. B., GELFAND, D. H. AND BROW, M. A. (1988) Proc. Natl. Acad. Sci. 85, 9436-9440.
  2. LAWYER, F. C., STOFFEL, S., SAIKI, R. K., MYAMBO, K., DRUMMOND, R. AND GELFAND, D. H. (1989) J. Biol. Chem. 264, 6427-6437.
  3. INNIS, M. A. AND GEFLAND, D. H. (1990) PCR Protocols: A Guide to Methods and Applications, Academic Press.

Applications:

  • Routine PCR amplification
  • Suitable for real time qPCR

Storage:

Shipped on dry ice. Store at -20°C.

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