Features:
- Anti-Taq (monoclonal antibody to Taq DNA polymerase) inhibits
the
reaction of Taq DNA Polymerases at room temperature
- Ideal as enhancer for PCR reactions or for "homemade" Hot-Start
Polymerase
Application:
Polymerase detergent/enhancer for:
- High specific amplification
- Multiplex amplification
- High sensitivity applications
- Low-copy number PCR
Unit definition:
One unit is defined as the amount required to blocks 50% activity of 1 µg of Polymerase
Note: The ratio units/mg of polymerase varies (up to factor of 10). The binding rate Anti-Taq
depends strongly of the polymerization region (active epitopes) of the polymerase. The optimized mixture has to be found in empiric test and for every new lot of polymerase, again.
Storage Buffer for S131/S132
20mM Tris-HCl (pH 7.0, at 22oC);50 mM KCl;0.1mM EDTA; 50% glycerol
Storage Buffer for S131/S132-8C1
3mM Tris-HCl (pH 8,0, @
22oC); 15 mM KCl; 0.1mM EDTA; 20 % Trehalose (pH 8,0, @ 22oC);
Concentration: 2-10 mg/ml
Units/mg-ratio:
2300 units of the specific polymerase activity are equal to 1 mg of antibodies
Storage: at – 20°C
Transportation: at room temperature or with blue ice
QC-Test: > 95% of protein in SDS electrophoresis in 15% PAAG
Name | Final conc., M | ||
Tris-HCl, pH 8,5 | 0,05-0,1 | ||
KCl | 0,05-0,1 | ||
MgCl2 | 0,01-0,0015 | ||
TMAC* | 0,015-0,034 | ||
Glycerol, % | from 3 to 6 | ||
BSA, mg/ml | 0,1-0,2 | ||
Tween 20, % | 0,15-0,2 | ||
DFS-Taq DNA polymerase, U/microliter | 0,05-0,1 | ||
Trehalose MABs, mg/ml Product-code: S131-S132-8C1 |
0,0036-0,0072 | ||
*TMAC - Tetramethylammonium chloride
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IMPORTANT: | |||
The proportion DFS PLUS Taq / m-AntiTaq should be 1 Unit to 0,06-0,072 µg MAB |
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Enhancer für Polymerasen, MAK zu Taq Polymerase
* availibility of sample size may be limited
Final price3
1.) R.T. D'Aquila, L.J. Bechtel, J.A. Videler, Eron JJ, P. Gorczyca, J.C.Kaplan, Maximizing sensitivity and specificity of PCR by pre-amplification heating. Nucleic Acids Res. 19: 3749 (1991)
2.) Q. Chou, M. Russell, D.E. Birch, J. Raymond, W. Bloch. Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications. Nucleic Acids Res. 20: 1717-23 (1992)
3.) D.E. Kellogg , I. Rybalkin, S. Chen, N. Mukhamedova, T. Vlasik, P.D. Siebert, A. Chenchik. TaqStart Antibody: "hot start" PCR facilitated by a neutralizing monoclonal antibody directed against Taq DNA polymerase. Biotechniques. 16: 1134-7 (1994)