Restriction Enzymes

SlaI (XhoI)

29,20 78,70 

SlaI is a restriction enzyme purified from Streptomyces lavendulae that cleaves the palindromic sequence CTCGAG.

Prototype (Isoschizomer): XhoI

Concentration: 10U/µL
Source: Stremptomyces lavendulae
Reagents supplied with: Buffer SH and the universal Simple Buffer for double digests. SlaI is also active in CutSmart® Buffer from NEB, 2x Tango™ Buffer from Thermo Fisher Scientific (Fermentas) or high salt buffers from other suppliers as long as the buffer is supplemented with 100µg/mL BSA.
Store at: -20 °C

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Unit definition: One unit is defined as amount of Sla I (Xho I) enzyme required to produce a complete digest of 1 µg Lambda DNA in 60 min in a total reaction volume of 50µL under the assay conditions.
Unit substrate: Lambda DNA/ HindIII digest
Unit calculation assay conditions: 1 µg Lambda DNA has been digested in 150mM NaCl, 1mM DTT, 10 mM Tris-HCl (pH 7.9 at 25 °C), 1mM dithiothreitol, 100 mM MgCl2, 100 µg/mL
Absence of contaminants: 50 units of SlaI do not produce any unspecific cleavage products after 16 hrs incubation with 1µg of Lambda DNA at 37 °C. After 10-fold overdigestion with SlaI, greater than 98% of the DNA fragments can be ligated and recut with this enzyme.
Storage buffer: SlaI is supplied in 50 mM KCl, 10 mM Tris HCl (pH 7.4), 0.1 mM EDTA, 1 mM dithiothreitol, 200 μg/ml BSA and 50% glycerol.
Inactivation: SlaI can be heat inactivated in 20min at 65 °C. The enzyme can be removed by spin column purification with PCR clean up kits. 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: Not sensitive

Activity in Simplebiotech buffers:

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

The Enzyme is supplied with 10x Buffer SH and the 10x universal Simple Buffer for double digests. The enzyme is also fully active in the respective buffers from other suppliers and may be used in double digests together with enzymes from other suppliers.
10x Buffer SH: 1500mM NaCl, 100mM Tris-HCl (pH 7.9 at 25 °C), 100mM MgCl2, 1mg/mL BSA
10x Simple buffer: 500 mM Potassium Acetate, 200 mM Tris-acetate (pH 7.9 at 25°C), 100 mM Magnesium Acetate, 1000 μg/ml BSA

Rapid digest within 15 minutes.

10x Buffer SH                              2 µL

DNA (0.5-1µg)                             1µL

10 U SlaI                                        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.

Referece: Takahashi, H., Shimizu, M., Saito, H., Ikeda, Y., & Sugisaki, H. (1979). A new site-specific endonuclease from Streptomyces lavendulae (SlaI). Gene, 5(1), 9-18.


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