Frequently bought together:
Description
abm | NotI | E051
N/A
Concentration:
20000 U/ml
Form:
N/A
Alternate Name:
N/A
Reaction Buffer:
Buffer 1: 25%, Buffer 2: 100%, Buffer 3: 25%, Universal Buffer: 100%
Click here to view the buffer compatibility chart for restriction enzymes.
Reaction:
1X Universal Restriction Enzyme Reaction Buffer. Incubate at 37°C
Notes:
T7 RNA Polymerase has high specificity for the T7 phage promoter and will not recognize SP6 or T3 RNA Polymerase promoter sequences.
Application:
- Students gain hands-on laboratory experience using the CRISPR gene-editing technique.
- Experiment performed in E. coli
- Simple and robust editing occurs in 4 days
- Uses standard reagents and equipment
Components:
N/A
Inactivation:
N/A
Source:
N/A
Shipping conditions:
Ice Packs
Storage conditions:
-20°C
Storag Buffer:
10 mM Tris-HCl (pH 7.5), 250 mM NaCl, 1 mM DTT, 0.1 mM EDTA, 0.15% Triton® X-100, and 50% (v/v) Glycerol
Discount(%):
30