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TAQ Polymerase

DNA Polymerase, TAQ – 1000U 

This product is a chemical substance and is intended to be used by persons having chemical knowledge and skill, at their own discretion and risk.

 

Chemical Product and Company Identification
Name
DNA Polymerase, TAQ                                                                      Cat # 11-BIO-21-40
Uses

DNA amplification via PCR

Product features

Highly processive 5'–3' DNA Polymerase

 

Extremely thermostable

 

Recombinant enzyme for best reproducible results

Hazards
Health: 1
Flammability: 0
Reactivity: 0
Company Identification
GENTAUR LABORATORIES                                           Avenue de l'Armée 68 
                                                                                             1040 Brussels, BELGIUM
                                                                                             Tel: +32 2 732 56 88
                                                                                             Fax: + 32 2 732 44 14
                                                                                             e-mail: info@gentaur.com
In case of Emergency
Call : GENTAUR                                            Tel : +32 (0) 2 732 56 88
Out of office:  Centre Antipoisons (Brussels) Tel:  +32 (0) 70 245 245

 

Identity Information

CAS Registry Number

9012-90-2

EC (EINECS/ELINCS)

232-741-2

 

Physical/Chemical Characteristics

Concentration

5 Unit/ul, 500Units/vial

Included

10X reaction buffer and 25mM MgCl2 buffer

Appearance

White to brown coloured liquid

Odour

Typical enzyme odour

Sources

Thermus aquaticus

Error rate

1/105

Unit definition

One unit incorporates 10 nmole of dNTP into acid-insoluble material in 30 min. at 74°C.
                                               QUALITY TESTING
Our Thermostable DNA Polymerase is highly purified, free of contaminating endonucleases, exonucleases and nicking activity. For endonuclease assay, 1 ug of Lambda/Hind III DNA is incubated with 20 units of the enzyme in assay buffer at 75°C for 16 hrs and no visible contaminating activity is observed; For exonucleases assay, 1 ug of pBR322 plasmid DNA is incubated with 10 units of enzyme for 16 hrs at 75°C in assay buffer and no detectable exonuclease is observed. The purity of the enzyme is also evaluated by adding 10 units of DNA polymerase in 100 ul of a reaction mixture for making first strand cDNA at beginning and no impaired effect on the first strand is observed.
                                               10X REACTION BUFFER(Without MgCl2)
500 mM KCl, 100 mM Tris HCl (pH 9.0) at 25°C, 1% Triton X-100 Buffer is optimized for use with 200 uM dNTPs
                                               25mM MgCl2 BUFFER
In general, 1.5-2.5 mM final concentration of MgCl2 is recommended.
*The final MgCl2 concentration may be variable according to individual experiment requirements.
                                               STORAGE BUFFER
20 mM Tris HCl ( pH 8.0 ), 0.l mM EDTA, lm M DTT, 0.1% Triton X-100, 50% glycerol
                                               EXTENSION CHARACTERISTIC
Our Thermostable DNA Polymerase has the independent terminal transferal activity which results in the addition of a single nucleotide ( adenosine ) at 3' end of the extension product. TA cloning vector is recommended if the extension product is needed to be cloned.

 

Storage

Storage Temperature

Store at -20°C and keep tightly closed.
                                                Warning
For Research Use Only. Not for drug, household or other uses. See Material Safety Data Sheet for additional information.

 

For more information :: Bioxys and Gentaur BVBA :: Av. de l'Armée 68 B4 :: BE-1040 BELGIUM

Email: info@gentaur.com
 

International 

+32 (0) 16 58 90 45

+32 (0) 16 50 90 45

France

01 43 25 01 50

01 43 25 01 60

Italy

02 36 00 65 93

02 36 00 65 94

Germany

0241 6085 13140

0241 6085 33033

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Copyright © 2005 Gentaur BVBA
Last modified: feb-07