Athens Research/Cambio - Excellence in Molecular Biology/50kU/PM-1210-02

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Enzymes for Molecular Biology

Enzymes for Molecular Biology: Enzymes for Molecular Biology

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  • Description
  • Protocols
  • References

S1 Nuclease (Aspergillus oryzae)

S1 Nuclease catalyses the release of 5"-phosphoryl mono- and oligonucleotides from single stranded nucleic acids

Cambio

Catalogue No.DescriptionPack SizePriceQty
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PM-1210-02S1 Nuclease50kU£550.00QuantityAdd to Order
PM-1210-10S1 Nuclease10kU£250.00QuantityAdd to Order

S1 Nuclease (Aspergillus oryzae)

S1 Nuclease catalyses the release of 5"-phosphoryl mono- and oligonucleotides from single stranded nucleic acids

Cambio

Source

Aspergillus oryzae

Applications

  • Catalyzes degradation of single-stranded nucleic acids into oligonucleotides and 5"-mononucleotides (1)
  • Cleaves both single-stranded DNA and RNA, with stronger DNAse activity
  • Double-stranded DNA, double-stranded RNA and DNA-RNA hybrids are resistant to degradation at moderate enzyme concentration
  • Capable of cleavage of double-stranded nucleic acids at nicks, mismatches and small gaps (2)
  • Relaxes/linearizes supercoiled plasmids
  • Removes protruding single-stranded ends
  • Can generate double-stranded DNA breaks in response to DNA nicks a basic sites
  • Used for S1 mapping of nucleic acids
  • Requires Zn²ions for activity
  • The enzyme is active up to 65°C

Unit Definition

One unit is the amount of enzyme required to convert 1µg of denatured calf thymus DNA to an acid soluble form in 1 minute at 37°C.

Storage Buffer

20 mM Sodium Acetate (pH 4.6)50 mM NaCl1 mM ZnCl2 50% (v/v) glycerol

Quality Control

All preparations are assayed for contaminating exonuclease and double-stranded DNase activities.

Storage Conditions

Store at -20°C

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

S1 Nuclease (Aspergillus oryzae)

S1 Nuclease catalyses the release of 5"-phosphoryl mono- and oligonucleotides from single stranded nucleic acids

Cambio

Download here

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

S1 Nuclease (Aspergillus oryzae)

S1 Nuclease catalyses the release of 5"-phosphoryl mono- and oligonucleotides from single stranded nucleic acids

Cambio

(1) Berg, A.J. et al. (1977) Cell 12, 721(2) Sambrook, J. et al. (1989) Molecular cloning: A laboratory Manual, second edition, pp. 5.78-5.79, Cold Spring Harbor, New York

If you cannot find the answer to your problem below then please contact us or telephone 01954 210 200

Myeloperoxidase Enzyme Immunoassay Kit 髓过氧化物酶 免疫分析试剂盒 Human MPO EIA KIT FEATURES: USE - Measure human MPO in a variety of matrices SAMPLE -Serum, Platelet-Poor Heparin Plasma, Saliva, Urine or Tissue Culture Media SAMPLES / KIT - 40 in duplicate SENSITIVITY - 0.068 ng/mL STABILITY - liquid reagents stable at 4°C QUICK RESULTS - 2.5 HOURS Myeloperoxidase (MPO) is a tetrameric heme-containing protein abundantly produced in neutrophil granulocytes where it plays an important anti-microbial role. During degranulation MPO is released into the extracellular space. There, as part of the neutrophils “respiratory burst”, it produces hypochlorous acid from hydrogen peroxide and Cl–. MPO also uses hydrogen peroxide to oxidize tyrosine to the tyrosyl radical. Both hypochlorous acid and tyrosyl are cytotoxic and when present can kill bacteria and other pathogens. Hereditary deficiency of myeloperoxidase predisposes individuals to immune deficiency. Studies have shown an association between elevated MPO levels and coronary artery disease, and in 2003 it was suggested that MPO may serve as a sensitive predictor of myocardial infarction in patients complaining of chest pain. Since that time the clinical utility of MPO testing in cardiac patients has been solidly established in the literature with well over 100 papers published. In 2010 this clinical application was further refined by additional studies which determined that measuring both MPO and C-reactive protein (CRP) provided more accurate prediction of mortality risk than measuring just CRP alone.