Athens Research/Cambio - Excellence in Molecular Biology/50 mini preps/GA-302-150

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Extraction & Purification - RNA

Extraction & Purification - RNA: Tissue/Cultures

RNA Isolation from tissues and cell cultures
  • Catalogue
  • Description
  • Protocols
  • References

Ribospin™ vRD

Ribospin™ vRD provides a convenient method for isolation of RNA and DNA from cell-free fluid, cell-culture supernatant, plasma, serum, swab, urine, and virus-infected samples. Ribospin™ vRD procedures employed the glassfiber membrane technology for the fastest and the most convenient of high purity RNA and DNA isolation, instead of conventional alcohol precipitation or phenol/chloroform extraction. Ribospin™ vRD buffer system provides the effective binding condition of RNA and DNA to glassfiber membrane through mix with lysis and binding buffers. And then the impurities on the membrane are washed away by two different wash buffers.....

GeneAll

Catalogue No.DescriptionPack SizePriceQty
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GA-302-150GeneAll Ribospin vRD50 mini preps£140.00QuantityAdd to Order

Ribospin™ vRD

Ribospin™ vRD provides a convenient method for isolation of RNA and DNA from cell-free fluid, cell-culture supernatant, plasma, serum, swab, urine, and virus-infected samples. Ribospin™ vRD procedures employed the glassfiber membrane technology for the fastest and the most convenient of high purity RNA and DNA isolation, instead of conventional alcohol precipitation or phenol/chloroform extraction. Ribospin™ vRD buffer system provides the effective binding condition of RNA and DNA to glassfiber membrane through mix with lysis and binding buffers. And then the impurities on the membrane are washed away by two different wash buffers.....

GeneAll

Description

Ribospin™ vRD provides a convenient method for isolation of RNA and DNA from cell-free fluid, cell-culture supernatant, plasma, serum, swab, urine, and virus-infected samples. Ribospin™ vRD procedures employed the glassfiber membrane technology for the fastest and the most convenient of high purity RNA and DNA isolation, instead of conventional alcohol precipitation or phenol/chloroform extraction. Ribospin™ vRD buffer system provides the effective binding condition of RNA and DNA to glassfiber membrane through mix with lysis and binding buffers. And then the impurities on the membrane are washed away by two different wash buffers. At last, pure RNA and DNA are eluted by nuclease-free water. Whole procedure may take only 20 minutes and the eluate is suitable for PCR, RT-PCR or any downstream application without further manipulation. Ribospin™ vRD plus! kit offers carrier RNA for purification of nucleic acid from very small amounts of sample.

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Features and Benefits

¦ Glassfiber membrane technology¦ Sample size : up to 300 uL¦ Preparation time : ~ 20 minutes¦ Stable and consistent yield¦ No phenol / chloroform extraction¦ No ethanol precipitation¦ Ready for use in PCR, RT-PCR, real-time PCR and other analytical procedures

Procedure

Specification

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

Ribospin™ vRD

Ribospin™ vRD provides a convenient method for isolation of RNA and DNA from cell-free fluid, cell-culture supernatant, plasma, serum, swab, urine, and virus-infected samples. Ribospin™ vRD procedures employed the glassfiber membrane technology for the fastest and the most convenient of high purity RNA and DNA isolation, instead of conventional alcohol precipitation or phenol/chloroform extraction. Ribospin™ vRD buffer system provides the effective binding condition of RNA and DNA to glassfiber membrane through mix with lysis and binding buffers. And then the impurities on the membrane are washed away by two different wash buffers.....

GeneAll

RibospinTM vRD (plus!) Protocol
RibospinTM vRD Protocol

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

Ribospin™ vRD

Ribospin™ vRD provides a convenient method for isolation of RNA and DNA from cell-free fluid, cell-culture supernatant, plasma, serum, swab, urine, and virus-infected samples. Ribospin™ vRD procedures employed the glassfiber membrane technology for the fastest and the most convenient of high purity RNA and DNA isolation, instead of conventional alcohol precipitation or phenol/chloroform extraction. Ribospin™ vRD buffer system provides the effective binding condition of RNA and DNA to glassfiber membrane through mix with lysis and binding buffers. And then the impurities on the membrane are washed away by two different wash buffers.....

GeneAll

List of references here

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.