DNase I, RNase-free, GMP-Grade (GMP-DNI-EE001), DMF #038032

  • Description: Digests single- and double-stranded DNA to oligonucleotides containing a 5' phosphate and 3'-hydroxylated ends
  • Applications: In Vitro Transcription (IVT)
    Removal of DNA from RNA samples
    DNase I footprinting
  • Quality: FDA Drug Master Files #038032
    Manufactured according to GMP guidelines
    High purity and tested for contaminating RNase and protease activities
    Suitable for the isolation of DNA-free RNA in diagnostic and mRNA therapeutics applications
  • Related Products: RNase-R, GMP-Ready
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    BsaI, GMP-Grade

Catalog: GMP-DNI-EE001

$438.00
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Product Description DNase I is an endonuclease that digests single- and double-stranded DNA to oligonucleotide containing a 5' phosphate and 3'-hydroxylated ends. It is an essential enzyme for the efficient digestion of DNA during RNA purification and is suitable for molecular diagnostics and in vitro mRNA synthesis applications.

This product has been submitted to the FDA Drug Master Files and is assigned DMF #038032.
Synonyms DNase1; DNase 1; DNaseI; Deoxyribonuclease I; DeoxyribonucleaseI; Deoxyribonuclease 1; Deoxyribonuclease1;
Application In Vitro Transcription (IVT)
Removal of DNA from RNA samples
DNase I footprinting
Concentration 4U/µL
Unit Definition One unit corresponds to the amount of enzyme required to produce a change in absorbance at 260 nm of 1.0 in 10 minutes.
Source Expressed in an E.coli strain with DNase I gene isolated from bovine pancreas.
Molecular Weight 39kD
Quality Standards Activity (Degradation plasmid method): ≥ 4 kU/mL
Purity (SEC-HPLC): ≥ 95%
Residual RNase: Negative
Residual Protease: Negative
Endotoxin: ≤ 1.2 EU/mL
Residual Host Cell DNA: ≤ 100 pg/mg
Residual Host protein: ≤ 20 ng/mg
Residual Heavy Metal: ≤ 10 ppm
Residual Nickel Salt: ≤ 10 ppm
Bioburden: ≤ 1 CFU/10 mL
Form Liquid
Shipping Shipping with dry ice
Stability And Storage -20C±5°C for 24 months.
Figure 1. 1µg DNA was added to various activity units of DNase I in a total reaction volume of 10µL. Compared with competitors 1 and 2, DNase I of KACTUS has a stronger digestive effect.
Figure 2. Different concentrations of ions were added to the transcriptional reaction. Results show DNase I is inhibited by Na+ and K+.

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