DNase I
Purified DNase I tested to be free of contaminating activity for the degradation of nucleic acids.
- RNase free
- Contains a mixture of four isoenzymes from bovine pancreas (10 units/µl)
DNase I, RNase Free catalyses the degradation of double-stranded DNA into oligonucleotides 1,2 and mononucleotides. This enzyme has been isolated as a mixture of four isoenzymes from bovine pancreas that cut preferentially next to pyrimidine nucleotides.
Reaction Conditions: 40 mM Tris-HCl (pH 7,5), 6 mM MgCl₂, 2 mM CaCl₂, 1 µg DNA and 1 unit enzyme in a 25 µl volume. Incubate 30 minutes at 37 °C.
: For research use only. Not for use in diagnostic procedures.
Purified DNase I tested to be free of contaminating activity for the degradation of nucleic acids.
- RNase free
- Contains a mixture of four isoenzymes from bovine pancreas (10 units/µl)
DNase I, RNase Free catalyses the degradation of double-stranded DNA into oligonucleotides 1,2 and mononucleotides. This enzyme has been isolated as a mixture of four isoenzymes from bovine pancreas that cut preferentially next to pyrimidine nucleotides.
Reaction Conditions: 40 mM Tris-HCl (pH 7,5), 6 mM MgCl₂, 2 mM CaCl₂, 1 µg DNA and 1 unit enzyme in a 25 µl volume. Incubate 30 minutes at 37 °C.
: For research use only. Not for use in diagnostic procedures.
- Catalog No:
- AGLS600031
- AGLS600032
- Nom de l'enzyme:
- DNase I
- DNase I
- Formulaire:
- Premixed
- Premixed
- Formulation:
- 10 mM Tris-HCl (pH 7,5), 10 mM CaCl₂, 10 mM MgCl₂ and 50 % glycerol (v/v). (Dilutions should be made in this buffer.)
- 10 mM Tris-HCl (pH 7,5), 10 mM CaCl₂, 10 mM MgCl₂ and 50 % glycerol (v/v). (Dilutions should be made in this buffer.)
Product Family Options
- Info cdtCdt
Specifications
Cat. No.AGLS600031Nom de l'enzymeDNase IFormulairePremixedFormulation10 mM Tris-HCl (pH 7,5), 10 mM CaCl₂, 10 mM MgCl₂ and 50 % glycerol (v/v). (Dilutions should be made in this buffer.)Specifications
Cat. No.AGLS600032Nom de l'enzymeDNase IFormulairePremixedFormulation10 mM Tris-HCl (pH 7,5), 10 mM CaCl₂, 10 mM MgCl₂ and 50 % glycerol (v/v). (Dilutions should be made in this buffer.)
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