SuperTherm DNA polymerase is a Thermostable DNA polymerase, purified fromThermus aquaticus strain by several rounds of chromatography. The purity of SuperTherm DNA polymerase is more than 90% of the total protein in the preparation. Amplification of DNA fragments (100bp to 5kb) can be achieved with it. The enzyme has both, 5′-3′ polymerase and 5′-3′ exonuclease activities.
Concentration : 5units /µl & 20units /µl
Storage : -20°C
| Ordering Information | ||
| Cat.No | Product | Units |
| MX-0647-01 | SuperTherm Taq DNA Polymerase (5u/ul) | 100U |
| MX-0647-02 | SuperTherm Taq DNA Polymerase (5u/ul) | 250U |
| MX-0647-03 | SuperTherm Taq DNA Polymerase (5u/ul) | 1000U |
| MX-0647-04 | SuperTherm Taq DNA Polymerase (20u/ul) | 250U |
| MX-0647-05 | SuperTherm Taq DNA Polymerase (20u/ul) | 1000U |
| MX-0647-06 | SuperTherm Taq DNA Polymerase | 10 x 1000u |
| Ordering Information | ||
| Cat.No | Product | Units |
| MX-0614-01 | DNA Amplification kit | 50 rxns |
DNA Amplification kit is used for the amplification of DNA fragments (100bp to 5kb). This kit contains all necessary components including Marker to perform PCR reactions. The reagents provided in this kit is sufficient for 50 PCR reactions except for control
DNA and Primer which are sufficient for 10 reactions.
Materials Provided
- Taq DNA Polymerase
- dNTPs
- 10X Reaction Buffer
- 25mM MgCl 2
- Control DNA
- Primer (Forward and Reverse) Match only to Control DNA
- DNA Marker
- Instruction Manual
Storage: -20 ° C
| Ordering Information | ||
| Cat.No | Product | Units |
| MX-0614-01 | DNA Amplification kit | 50 rxns |
Supplied with 5X Reaction Buffer
Purified from an E.coli strain carrying a Moloney Murine Leukemia Virus (M-MuLV) reverse transcriptase overproducing plasmid. M-MuLV is an RNA and DNA dependent DNA polymerase. The enzyme also exhibits RNase H activity, catalyzes 5′ to 3′ synthesis of DNA. The enzyme exhibits 3′ to 5′ exonuclease activity.
Unit Definition : 1 unit of enzyme catalyzes the incorporation of 1 nanomoles of dTTP into acid insoluble form in 10 min at 37°C using poly(Ra) oligo(dT) as the template primer
Concentration : 50U/µl
Reaction Buffer : 50mM Tris-HCl (pH8.3), 75mM KCl, 3mM MgCl2, 10mM DTT
Storage Buffer : 50mMTris-HCl (pH 8.3),1mM EDTA, 0.1mM DTT, 0.1% NP-40, 0.1mM NaCl and 50% glycerol
Storage : -20°C
| Ordering Information | ||
| Cat.No | Product | Units |
| MX-0717-02 | M-MuLV Reverse Transcriptase | 1000U |
| MX-0717-03 | M-MuLV Reverse Transcriptase | 5000U |
| MX-0717-04 | M-MuLV Reverse Transcriptase | 10000U |
SuperTherm DNA polymerase is a Thermostable DNA polymerase, purified fromThermus aquaticus strain by several rounds of chromatography. The purity of SuperTherm DNA polymerase is more than 90% of the total protein in the preparation. Amplification of DNA fragments (100bp to 5kb) can be achieved with it. The enzyme has both, 5′-3′ polymerase and 5′-3′ exonuclease activities.
Concentration : 5units /µl & 20units /µl
Storage : -20°C
| Ordering Information | ||
| Cat.No | Product | Units |
| MX-0647-01 | SuperTherm Taq DNA Polymerase (5u/ul) | 100U |
| MX-0647-02 | SuperTherm Taq DNA Polymerase (5u/ul) | 250U |
| MX-0647-03 | SuperTherm Taq DNA Polymerase (5u/ul) | 1000U |
| MX-0647-04 | SuperTherm Taq DNA Polymerase (20u/ul) | 250U |
| MX-0647-05 | SuperTherm Taq DNA Polymerase (20u/ul) | 1000U |