JumpStart™ Taq DNA Polymerase
SIGMA/D4184 - without MgCl2
Synonym: hot start DNA polymerase; hot start PCR
MDL Number: MFCD00166026
Product Type: Chemical
| application(s) | agriculture |
| color | colorless |
| concentration | 2.5 units/μL |
| feature | dNTPs included: no |
| hotstart | |
| form | liquid |
| input | purified DNA |
| Quality Level | 300 ![]() |
| shipped in | wet ice |
| storage temp. | −20°C |
| suitability | suitable for PCR |
| technique(s) | PCR: suitable |
| usage | sufficient for 1500 reactions |
| sufficient for 250 reactions | |
| sufficient for 50 reactions |
| Application: | • For PCR amplifications that require reduced non-specific amplification • For multiplex PCR • For reduction of primer dimers |
| Application: | JumpStart™ Taq DNA polymerase has been used: • In the PCR amplification of DNA isolated from herbarium specimens. • In the PCR reaction mixture for randomly amplified polymorphic DNA polymerase chain reaction (RAPD PCR). • To amplify and detect a point mutation in the EGFR exon 19 using specific cancer cell lines. • In real-time quantitative PCR • For PCR amplification of complex genomic or cDNA templates • For the PCR amplification of very low-copy number targets • For the PCR amplification of many thermal cycles (>35), and multiple primer pairs in the same reaction tube |
| Features and Benefits: | • Reduces non-specific amplification • Increases PCR specificity and yield • Reduces set-up time concerns associated with manual or wax Hot Start methods • Activation time of less than 1 minute |
| General description: | The Taq DNA polymerase activity is inactivated by combining the enzyme with JumpStart™ Taq antibody, a neutralizing monoclonal antibody to Taq DNA polymerase. Antibody inactivation provides a simple, efficient procedure for hot-start polymerase chain reaction (PCR). Hot start PCR can significantly improve the results of DNA amplification by reducing the generation of nonspecific amplification products and primer-dimer artifacts. When used in PCR, JumpStart Taq DNA polymerase is inactive at low (room) temperature. When the temperature is raised above 70 °C in the first denaturation step of the cycling process, the complex dissociates and the polymerase becomes fully active. |
| Legal Information: | JumpStart is a trademark of Sigma-Aldrich Co. LLC |
| Legal Information: | Use of this product is covered by one or more of the following US patents and corresponding patent claims outside the US: US 8,404,464 and US 7,972,828. The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims. Antibody licensed for in vitro research use under U.S. Patent No. 5,338,671 and 5,587,287, and corresponding patents in other countries. |
| Other Notes: | One unit incorporates 10 nmol of total dNTPs into acid-precipitable DNA in 30 min at 74 °C. |
| Other Notes: | Sigma′s JumpStart Taq DNA Polymerase is an antibody-inactivated hot-start enzyme designed to minimize non-specific amplification while increasing target yield. Once the reaction temperature reaches 70°C, Taq DNA polymerase activity is restored and the resulting PCR exhibits a higher specificity and yield. This antibody-enzyme complex allows for easy and convenient set-up with less contamination risk than manual hot-start techniques. The enzyme may also be included in the master mix preparation resulting in more consistency from one reaction to the next. |
| Other Notes: | View more detailed information on JumpStart Taq enzymes at www.sigma-aldrich.com/hot . |
| Packaging: | JumpStart Taq DNA Polymerase is provided with a 10× reaction buffer available with and without MgCl2. The magnesium free 10× buffer also includes a separate tube of 25 mM MgCl2 for optimization. |
| Packaging: | Supplied with 10× reaction buffer without MgCl2. Includes a separate tube of 25 mM MgCl2 |
| RIDADR | NONH for all modes of transport |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | −20°C |
| UNSPSC | 12352204 |

