11480022001
Roche
Tth DNA Polymerase
pkg of 500 U (2 x 250_U), sufficient for ≤200 reactions
Synonyma:
DNA polymerase, polymerase
About This Item
Doporučené produkty
biological source
bacterial (Thermus thermophilus)
Quality Level
recombinant
expressed in E. coli
form
liquid
usage
sufficient for ≤200 reactions
specific activity
5 U/μL
packaging
pkg of 500 U (2 x 250_U)
manufacturer/tradename
Roche
concentration
0.5-5.0 units (per reaction for PCR (standard))
2.5 units (per reaction for PCR (standard))
parameter
75 °C optimum reaction temp.
technique(s)
PCR: suitable
RT-PCR: suitable
nucleic acid labeling: suitable
color
colorless
optimum pH
~9.0 (25 °C)
solubility
water: miscible
suitability
suitable for molecular biology
UniProt accession no.
application(s)
life science and biopharma
foreign activity
Endonuclease, none detected (up to 20 enzyme units using Lambda-DNA/ 16h/37°C)
Nicking activity, none detected ( up to 20 enzyme units using pBR322-DNA / 16h/37°C)
RNases, none detected (up to 20 enzyme units using MS II-RNA; 4h/37°C)
storage temp.
−20°C
General description
Application
- to amplify DNA fragments by polymerase chain reaction (PCR) due to its resistance towards prolonged incubations at high temperatures (95 °C)
- to label DNA fragments with either radiolabeled nucleotides, digoxigenin, or biotin, since this enzyme accepts modified deoxyribonucleotides as substrates
- to efficiently transcribe RNA targets into cDNA due to its intrinsic Mn-dependent reverse transcriptase (RT) activity
- for real time PCR
Biochem/physiol Actions
Features and Benefits
- Ensures optimized polymerase chain reaction (PCR) product size for at least up to 1,000 bp in a RT-PCR reaction
- Accepts modified desoxyribonucleoside triphosphates as substrates
- Has no association with RNase H activity
- Has high thermostability to overcome the problem, typically associated with the high degree of secondary structure present in RNA
Packaging
Quality
Unit Definition
Unit Assay: Incubation buffer for assay on activated DNA
67 mM Tris-HCI, pH 8.8 (+25 °C), 16.6 mM (NH4)2SO4, 6.7 mM MgCl2, 10 mM 2-mercaptoethanol, 0.2 mM dATP, dCTP, dGTP, dTTP each.
Incubation procedure
12.5 μg activated herring sperm DNA and 0.1 μCi [α32P] dCTP are incubated with 0.01 to 0.1 units Tth DNA Polymerase in 50 μl Incubation buffer with a paraffin oil overlay at +70 °C for 30 min.
The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation followed by scintillation counting.
Volume Activity: 0.5 to 5 U per reaction of PCR (optimal)
2.5 U per reaction of PCR (standard)
Determined in the assay on activated DNA described under "unit assay".
Other Notes
Legal Information
Pouze součásti soupravy
- PCR Buffer, including MgCl2 10x concentrated
- RT-PCR Buffer, coupled reaction in one tube 5x concentrated
- Mn(OAc)2-Solution 25 mM
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
does not flash
flash_point_c
does not flash
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