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    DNA酶I 來源于牛胰腺無RNase & Protease,溶液), ≥2,000 Kunitz units/ml
    產(chǎn)品基本信息
    產(chǎn)品編號:D128590
    產(chǎn)品名稱:DNA酶I 來源于牛胰腺無RNase & Protease,溶液), ≥2,000 Kunitz units/ml
    產(chǎn)品CAS:9003-98-9
    規(guī)格含量:500UN
    產(chǎn)品價格:1800
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    產(chǎn)品詳細(xì)介紹

      DNA酶I 來源于牛胰腺無RNase & Protease,溶液), ≥2,000 Kunitz units/ml

      Product Name: Deoxyribonuclease I from Bovine Pancreas(RNase & Protease Free,Solution)
      別名:脫氧核糖核酸酶 I;脫氧核糖核酸 5′-寡核苷酸-水解酶
      CAS號:9003-98-9
      介紹: Bovine pancreatic deoxyribonuclease is an endonuclease which splits phosphodiester linkages, preferentially adjacent to a pyrimidine nucleotide yielding polynucleotides with free hydroxyl group at the 3' position and phosphate group at the 5' position. The average chain length of a limit digest is a tetranucleotide.
      用途: 用于從蛋白質(zhì)樣品中除去 DNA。 Deoxyribonuclease I from bovine pancreas has been used in a study to compare several procedures for reducing RNase contamination in preparations of DNase. Deoxyribonuclease I from bovine pancreas has also been used in a study to investigate the effect of the composition of sodium dodecyl sulfate preparations on the renaturation of enzymes after polyacrylamide gel electrophoresis.
      貯存: 儲存溫度-20°C
      生化和生理學(xué)機(jī)理: DNase I is an endonuclease that acts on phosphodiester bonds adjacent to pyrimidines to produce polynucleotides with terminal 5′-phosphates. In the presence of Mg2+, DNAse I cleaves each strand of DNA independently and the cleavage sites are random. Both DNA strands are cleaved at approximately the same site in the presence of Mn2+. Divalent cations such as Mn2+, Ca2+, Co2+, and Zn2+ are activators of the enzyme. A concentration of 5 mM Ca2+ stabilizes the enzyme against proteolytic digestion. The pH optimum is found to be between 7 and 8. DNAse I from bovine pancreas consists of four chromatographically distinguishable components, A, B, C, and D, with their molar ratios being 4:1:1 respectively. Only minor amounts of D are found. 2-Mercaptoethanol, chelators, sodium dodecyl sulfate (SDS)6 and actin7 are known to inhibit the enzyme activity.


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