Restriction Enzymes


49,90 388,50 

NotI is a restriction enzyme purified from Nocardia otitidis-caviarum that cleaves the palindromic sequence GCGGCCGC.

Concentration: 10U/µL

Source: Nocardia corallina

Reagents supplied with: The Enzyme is supplied with 10x UniqueNotI Buffer. The enzyme is also fully active in the respective buffers from other suppliers.

Store at: -20 °C

Qualified for rapid digest in just 15 minutes.

Lieferzeit: Lieferzeit 1-2 Werktage

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Reagents supplied with: UNotI buffer

Contents 10x UNotI: 500 mM Tris-HCl (pH 7.9 at 25 °C), 1000mM NaCl, 50mM MgCl2, 1mg/mL BSA
Activity in Simplebiotech buffers:

L M H SH Simple 2x Simple
<10  25-50 75-100 75 50 100


Rapid digest within 15 minutes.

10x UNotI buffer                      2 µL
DNA (0.5-1µg)                          1µL
10 U NotI                                   1 µL
Nuclease free water            16 µL
                                Final volume 20µL

Incubate at 37 °C for 15 minutes.

Always add the restriction enzymes as last component. Mix gently but thoroughly by pipetting up and down or flicking. Spin down.
Incubate at 37 °C for 15min. Restriction enzymes are stored in 50% glycerol. The glycerol concentration in the reaction mix should not exceed 10%. When digesting more than 1µg DNA, scale up the restriction mix or prolong the incubation time.

Unit definition: One unit is defined as amount of NotI enzyme required to produce a complete digest of 1 µg Adenovirus-2 DNA DNA in 60 min in a total reaction volume of 50µL under the assay conditions.
Unit substrate: Adenovirus-2 DNA.
Unit calculation assay conditions: 100 mM NaCl, 50 mM Tris-HCl (pH 7.9 at 25°C), 5mM MgCl2, 1mM DTT, 100 µg/mL bovine serum albumin.
Absence of contaminants: 50 units of NotI do not produce any unspecific cleavage products after 16 hrs incubation with 1µg of Adeno-2 DNA at 37 °C. After 30-fold overdigestion with NotI, greater than 98% of the DNA fragments can be ligated and recut with this enzyme.
Storage buffer: NotI is supplied in 500 mM KCl, 10 mM TrisHCl (pH 7.4), 0.1 mM EDTA, 1 mM dithiothreitol, 0.1% Triton, 500 μg/ml BSA and 50% glycerol.
Inactivation: Heat to 65 °C for 20 minutes. It is also possible to stop the digest by addition of EDTA to a final concentration of >10mM or SDS to a concentration of 0.1 %. Alternatively use our environmentally friendly 6x orange gel loading buffer. For further enzymatic reactions remove SDS or EDTA by spin column-based PCR purification kit.
Methylation Sensitivity:

dam methylation: Not sensitive

dcm methylation: Not sensitive

CpG methylation: Blocked


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