Product Name | Code No. | Size | Price | Note |
---|---|---|---|---|
Gene Taq FP |
311-04164 |
50 units |
||
Gene Taq FP |
317-04161 |
250 units |
||
Gene Taq FP |
313-04163 |
250 units x 4 |
Gene Taq FP is obtained by purifying Gene Taq to a higher purity by a unique technique in which contamination by genomic DNA derived from the host bacteria is controlled as much as possible. This product possesses similar functions as Gene Taq and is characterized by having a high amplification efficiency of DNA fragments of not more than 1 kbp and having no 5'-3' exonuclease activity. Also, having a terminal transferase activity, the PCR product obtained can be used for TA cloning.
Molecular Weight | 68 kDa |
---|---|
Concentration | 5 units/μl |
Storage Conditions | 20 mmol/l Tris-HCl (pH 8.0), 100 mmol/l KCl, 0.1 mmol/l EDTA, 0.5% Tween 20, 1 mmol/l DTT, 50% Glycerol |
Unit Definition | One unit is defined as the enzyme activity incorporating 10 nmoles of deoxynucleotide into acid-insoluble precipitates at 74°C for 30 min using activated calf thymus DNA as a primer/template. |
Purity | No change was observed in the agarose gel electrophoresis pattern of DNA after reacting 10 units of this enzyme and 1 µg of λ/Hind III digest at 74°C for 1 hr. |
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Component | Quantity | Storage | Description |
---|---|---|---|
Gene Taq FP | 50 units x 1 | -20°C | |
dNTP Mixture (2.5 mmol/l each) | 160 μl x 1 | -20°C | |
10 x Gene Taq Universal Buffer (15 mmol/l Mg2+) | 1 ml x 1 | -20°C |
Component | Quantity | Storage | Description |
---|---|---|---|
Gene Taq FP | 250 units x 1 | -20°C | |
dNTP Mixture (2.5 mmol/l each) | 800 μl x 1 | -20°C | |
10 x Gene Taq Universal Buffer (15 mmol/l Mg2+) | 1 ml x 1 | -20°C |
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Product | Characteristics | 5' → 3' exonuclease activity | terminal transferase activity |
---|---|---|---|
Gene Taq | The amplification efficiency of DNA fragments not more than 1 kbp is especially high. | - |
+ |
Gene Taq NT | Gene Taq NT has the same functions as natural Taq DNA polymerase. | + |
+ |
Gene Taq FP | Gene Taq FP obtained by further purifying Gene Taq to a higher degree of purity and by controlling the contamination by the host-derived DNA as much as possible. It is suitable for RAPD PCR which is affected by contamination by the genomic DNA. |
- |
+ |