• mRNA generation for in vitro translation systems
• Supplied with 10X Reaction Buffer
Description: SP6 RNA Polymerase catalyzes the synthesis of RNA in the 5´→ 3´ direction in the presence of a DNA template containing an SP6 phage promoter. SP6 RNA Polymerase can be used to generate high specific activity labeled RNA probes, RNA for in vitro translation, biologically active mRNA and/or preparative quantities of defined length RNA by run off transcription (1).
Source: An E. coli strain that carries the cloned gene for SP6 RNA Polymerase from Salmonella typhimurium LT2Z.
Applications:
Radiolabeled RNA probe preparation (2)
RNA generation for in vitro translation (3)
RNA generation for studies of RNA structure, processing and catalysis (3)
Expression control via anti-sense RNA
Reagents Supplied: RNAPol Reaction Buffer (10X)
Reaction Conditions: 1X RNAPol Reaction Buffer Supplemented with 0.5 mM ATP, 0.5 mM Guanosine triphosphate, 0.5 mM UTP, and 0.5 mM CTP Incubate at 40°C.
1X RNAPol Reaction Buffer: 40 mM Tris-HCl
6 mM MgCl2
10 mM Dithiothreitol
2 mM spermidine
pH 7.9 @ 25°C
Unit Definition: One unit is defined as the amount of enzyme that will incorporate 1 nmol ATP into acid-insoluble material in a total reaction volume of 50 μl in 1 hour at 40°C in 1X RNA Polymerase Reaction Buffer.
Concentration: 20,000 units/ml
Storage Conditions: 50 mM Tris-HCl
100 mM NaCl
20 mM 2-Mercaptoethanol
1 mM EDTA
50% Glycerol
0.1% Triton X-100
pH 7.9 @ 25°C
原厂资料:
• Isolated from a recombinant source
• RNA probe preparation for hybridization
• mRNA generation for in vitro translation systems
• Supplied with 10X Reaction Buffer
Description: SP6 RNA Polymerase catalyzes the synthesis of RNA in the 5´→ 3´ direction in the presence of a DNA template containing an SP6 phage promoter. SP6 RNA Polymerase can be used to generate high specific activity labeled RNA probes, RNA for in vitro translation, biologically active mRNA and/or preparative quantities of defined length RNA by run off transcription (1).
Source: An E. coli strain that carries the cloned gene for SP6 RNA Polymerase from Salmonella typhimurium LT2Z.
Applications:
Radiolabeled RNA probe preparation (2)
RNA generation for in vitro translation (3)
RNA generation for studies of RNA structure, processing and catalysis (3)
Expression control via anti-sense RNA
Reagents Supplied: RNAPol Reaction Buffer (10X)
Reaction Conditions: 1X RNAPol Reaction Buffer Supplemented with 0.5 mM ATP, 0.5 mM Guanosine triphosphate, 0.5 mM UTP, and 0.5 mM CTP Incubate at 40°C.
1X RNAPol Reaction Buffer: 40 mM Tris-HCl
6 mM MgCl2
10 mM Dithiothreitol
2 mM spermidine
pH 7.9 @ 25°C
Unit Definition: One unit is defined as the amount of enzyme that will incorporate 1 nmol ATP into acid-insoluble material in a total reaction volume of 50 μl in 1 hour at 40°C in 1X RNA Polymerase Reaction Buffer.
Concentration: 20,000 units/ml
Storage Conditions: 50 mM Tris-HCl
100 mM NaCl
20 mM 2-Mercaptoethanol
1 mM EDTA
50% Glycerol
0.1% Triton X-100
pH 7.9 @ 25°C