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Dnase Ⅰ;Deoxyribonuclease I(Bovine pancrease);Deoxyribonucleate 5′-oligonucleotido-hydrolase

CAS No.: 9003-98-9
Item No.: E0046
Store at: -20℃

English name:Dnase Ⅰ;Deoxyribonuclease I(Bovine pancrease);Deoxyribonucleate 5′-oligonucleotido-hydrolase
Other names: Deoxygenated cell nuclease; Oxyribonucleic acid-5 ˊ- Oligonucleotide hydrolase; Ribonuclease free; Deoxyribonucleic acid polymerase; Deoxyribonuclease (bovine pancreas); Deoxygenated cell nuclease (bovine pancreas); DNase

Grade:BR
Molecular weight:38KDa
Vitality:≥300Kunitz U/mg

Definition of activity: At 25 ℃, the amount of enzyme that catalyzes high molecular DNA solution to increase the absorbance at 260nm by 0.001 per minute is an active unit

Loss on drying: < 5.0%

Ignition residue: < 1.0%

Physicochemical properties: White or off white lyophilized powder. It is a double stranded specific endonuclease, which can degrade double stranded DNA into 5 ˊ- Phosphoric acid and 3 ˊ- OH terminal oligodeoxyribonucleotides. Single stranded DNA can also be degraded in the presence of monovalent manganese ions. Soluble in water, slightly soluble in 30% ethanol and acetone. Enzyme reaction: deoxyribonucleic acid → dinucleotide 5 ′ phosphate + oligonucleotide 5 ′ phosphate, the optimum pH is 7.8.Light absorption coefficient (E1% 280) 11.1. The activator is divalent metal ions, and the maximum activation can be obtained from magnesium (Mg2 +) + calcium (Ca2 +). The inhibitors are EDTA and sodium dodecyl sulfate. 5mmol / L calcium (Ca2 +) can be added.

Purpose: Biochemical research. For molecular biology research. Various enzymes that degrade DNA.

These enzymes hydrolyze the phosphate diester bond on the sugar phosphate main chain. There are two kinds of enzymes: exonuclease and endonuclease. There are many kinds of DNAase, some are single chain specific, some are double chain specific, or sequence specific (such as restriction endonuclease). Restriction endonuclease has the ability to recognize specific base sequences, which has been used in gene manipulation technology to construct artificial clones.

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