PI88216

Thermo Scientific™ Micrococcal Nuclease Solution (≥100 U/μL)

Manufacturer: Thermo Scientific™

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Pack Size SKU Availability Price
Each of 1 PI88216-Each-of-1 In Stock ₹ 19,507.68

PI88216 - Each of 1

₹ 19,507.68

In Stock

Quantity

1

Base Price: ₹ 19,507.68

GST (18%): ₹ 3,511.382

Total Price: ₹ 23,019.062

Product Type

Cell Lysis Enzyme

Form

Liquid

Quantity

150 μL

Content And Storage

Upon receipt store at -20°C. Product is shipped with dry ice.

Reagent Type

Enzyme for Cell Lysis

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Description

  • Thermo Scientific™ Micrococcal Nuclease (MNase) is suitable for removing nucleic acids from cell lysates, releasing chromatin-bound proteins and shearing chromatin for use in chromatin immunoprecipitation (ChIP) experiments
  • This micrococcal nuclease is a stable liquid form of the enzyme derived from Staphylococcus aureus
  • Micrococcal nuclease (MNase) exhibits exo- and endo-5'-phosphodiesterase activities against DNA and RNA
  • This enzyme digests double-stranded, single-stranded, circular and linear nucleic acids
  • The highest activity is toward single-stranded nucleic acid substrates with preference for AT- or AU-rich regions
  • Enzymatic activity occurs at pH 7 to 10 and is strictly dependent on calcium for the digestion of RNA and DNA substrates
  • Micrococcal nuclease is suitable for removing nucleic acids from cell lysates, releasing chromatin-bound proteins and shearing chromatin for use in chromatin immunoprecipitation (ChIP) experiments
  • Highlights: Digests nucleic acids (DNA and RNA) Effective for double-stranded, single-stranded, circular and linear nucleic acids Active in neutral to alkaline buffer conditions containing divalent calcium ions Supplied at ≥100 units/μL in 10mM Tris-HCl, pH 7.5, 50mM NaCl, 1mM EDTA, 50% glycerol Compatible with: Thermo Scientific Subcellular Protein Fractionation Kit (Part No
  • 78840); Thermo Scientific Pierce ChIP Kit (Part No
  • 26156) Recommended for: Enzymatic DNA shearing for chromatin immunoprecipitation assays (ChIP); Removal of unwanted genomic or organellar nucleic acids from cell lysates; Degradation of nucleic acids in subcellular fractionation procedures

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