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biological source
bacterial (Thermus aquaticus BM)
recombinant
expressed in E. coli
form
liquid
usage
sufficient for ≤2,000 reactions (11647687001), sufficient for ≤500 reactions (11647679001)
specific activity
1 U/μL
mol wt
~95 kDa
feature
dNTPs included: no, hotstart: no
packaging
pkg of 1,000 U (11647687001 [4 x 250 U]), pkg of 250 U (11647679001)
manufacturer/tradename
Roche
concentration
25 U/mL, 30 U/mL
parameter
72 °C optimum reaction temp.
technique(s)
PCR: suitable
color
colorless
input
purified DNA
optimum pH
~9.0 (20 °C)
solubility
water: miscible
suitability
suitable for PCR, suitable for molecular biology
NCBI accession no.
UniProt accession no.
application(s)
genomic analysis
life science and biopharma
foreign activity
Endonucleases 20 units, none detected, Nicking activity 20 units, none detected
storage temp.
−20°C
General description
The high processivity, absence of exonuclease activity and temperature optima of Taq DNA Polymerase enable the use of this enzyme in DNA sequencing, especially where the resolution of secondary structures plays a major role.
Application
Packaging
Other Notes
Unit Assay: Incubation buffer:
67 mM Tris/HCl; pH 8.3/25 °C, 5 mM MgCl2, 10 mM Mercaptoethanol, 0.2% Polydocanol, 0.2 mg/ml Gelatine, 0.2 mM each dATP, dGTP, dTTP and 0.1 mM dCTP.
Incubation procedure:
M13mp9ss, M13 primer (17mer) and 1 μCi (α-32P) dCTP are incubated with suitable dilutions of Taq DNA Polymerase in 50 μl incubation buffer at +65 °C for 60 minutes. The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation.
Volume Activity: 1 U/μl
Legal Information
Tylko elementy zestawu
- Taq DNA Polymerase 1 U/μl
- PCR Buffer with MgCl<sub>2</sub> 10x concentrated
- MgCl<sub>2</sub> Stock Solution
- PCR Buffer without MgCl<sub>2</sub>
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
Klasa składowania
12 - Non Combustible Liquids
wgk
WGK 2
flash_point_f
does not flash
flash_point_c
does not flash
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