BP8018-1

OPTIZYME™ SpeI (BcuI), Fisher BioReagents™

Manufacturer: Fischer Scientific

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Concentration

10 U/μL

Incubator Temperature

37°C

For Use With (Application)

>95% of DNA fragments can be ligated and re-cut after 50-fold over-digestion with SacI

Quantity

400 U

Product Type

SacI

Components

10X OPTIZYME™ Ecl136II, SacI Buffer

pH

7.4

Storage Buffer

10mM Tris HCl (pH 7.4 at 25°C), 100mM KCl, 1mM EDTA, 1mM DTT, 0.2mg/mL BSA, 50% Glycerol

Cut Site

A.CTAGT

Form

Liquid

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Description

  • 5'...A^C T A G T...3' 3'...T G A T C^A...5' Supplied with: 10X OPTIZYME Buffer 4 Conditions for 100% Activity: 1X OPTIZYME Buffer 4: 33mM Tris-acetate (pH 7.9 at 37°C), 10mM Mg-acetate, 66mM K-acetate and 0.1mg/ml BSA Incubate at 37°C Enzyme Activity in OPTIZYME buffers: Buffer 1: 50 - 100% Buffer 2: 50 - 100% Buffer 3: 0 - 20% Buffer 4: 100% Buffer 5: 20 - 50% Storage Buffer: 10mM Tris-HCl (pH 7.5 at 25°C), 300mM KCl, 1mM DTT, 0.1mM EDTA, 0.2mg/ml BSA and 50% (v/v) glycerol Ligation and Re-cleavage: More than 80% of the DNA fragments can be ligated and more than 90% of these can be re-cut after 50-fold over-digestion with SpeI
  • Digestion of Agarose-embedded DNA: A minimum of 10 units of SpeI is required for the complete digestion of 1μg of agarose-embedded Adenovirus-2 DNA in 16 hours
  • Note: Assayed using pUC19 DNA with insert, containing BcuI recognition site
  • Compatible Ends: XmaJI, Eco130I, NheI, XbaI Methylation Effects: Dam: Never overlaps - no effect Dcm: Never overlaps - no effect CpG: Never overlaps - no effect EcoKI: May overlap - effect not determined EcoBI: May overlap - effect not determined

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Concentration:
10 U/μL

Incubator Temperature:
37°C

For Use With (Application):
>95% of DNA fragments can be ligated and re-cut after 50-fold over-digestion with SacI

Quantity:
400 U

Product Type:
SacI

Components:
10X OPTIZYME™ Ecl136II, SacI Buffer

pH:
7.4

Storage Buffer:
10mM Tris HCl (pH 7.4 at 25°C), 100mM KCl, 1mM EDTA, 1mM DTT, 0.2mg/mL BSA, 50% Glycerol

Cut Site:
A.CTAGT

Form:
Liquid

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