1288.00
SapI SapI限制性内切酶 替代NEB R0569S NEB R0569L
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SapI SapI限制性内切酶 替代NEB R0569S NEB R0569L


SapI   is a restriction endonuclease that recognizes the sequence GCTCTTCN^NNN_.. BspQ I (10 U/μl) and 10X BspQ I Buffer are included.


Product Information

Source

E.coli  

Restriction Enzyme Cutting Site

5’…GCTCTTC(N)1↓…3’

3’…CGAGAAG(N)4↑…5’

Storage Buffer

10 mM Tris-HCl, 300 mM NaCl, 1 mM DTT, 0.1 mM EDTA, 500 μg/ml HSA, 50% Glycerol, pH 7.4

Enzyme Activity Definition

One unit is defined as the amount of enzyme required to digest 1 µg of λ DNA in 1 hour at 37°C in a total reaction volume of 50 µl.

Transportation/Storage Condition

Dry ice transport, store at -20 ± 5 °C. Avoid repeated freeze-thaw cycles  

Product Applications

Molecular cloning, restriction site mapping, genotyping, SNPs, etc.  


Specifications

ComponentsCat. #/Size
SAP-DL101-1000 USAP-DL101-1000 U
SapI (10 U/μl)SAP-DL101-E (100 μl)SAP-DL101-E (1ml)
10×Cut Reaction BufferCUT-DL001-B8 (800 μl)CUT-DL001-B80 (8ml)


Assay Data

SapI -1.png

Fig. 1 The digestion efficiency of DiLab SapI is greater than competitor, and basically equivalent to the BspQI digestion efficiency of the competitor. 1 μg plasmid was added to 1 μl SapI/BspQI (lane NC was control, lane 1 - 4 diluted at 2 times gradient, lane 1 was stock solution) in a 15 min at 37°C/50°C with a total reaction volume of 50 μl.


SapI -2.png

Fig. 2 1 μg plasmid was added to 1 μl SapI (lane NC was control, lane 1 - 5 diluted at 2 times gradient, lane 1 was stock solution) in a 16 h at 37°C with a total reaction volume of 50 μl.


Cautions

(1) BspQI is insensitive to Dam, Dcm, and CpG methylation.
(2) Before the enzymatic digestion reaction, try to ensure that the DNA does not contain impurities such as phenol, chloroform, alcohol, EDTA, etc., so as not to affect the enzymatic digestion effect.



提示:本产品仅供工业应用或科学研究使用!


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小递价格
1288.00
所属品牌
DiLab
来源
E. coli
纯度
10 U/μl,以每批次为准
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