KIT MIDI FLOW ILLUSTRA BLOOD GENOMICPREP 1 * 50 Tes (GE HEALTHCARE)

ویرایش
90.5.27

تاریخ اعتبار
90.7.27

لطفا پس از پایان اعتبار قیمت با شماره تلفن 88748085 تماس حاصل فرمائید

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Technical Information


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Real-time PCR amplification from genomic DNA extracted from K3 EDTA-treated whole blood using the illustra blood genomicPrep Mini Spin Kit. The eluted product (3 μl ) and various amounts (0.1, 1, 10, and 100 ng) of control DNA were amplified using chromosome-specific primers in a real-time PCR assay on an ABI 7900. Replicates were n = 3.

The purification process involves minimal shearing resulting in the production of 5 to 10 μg of good quality, intact genomic DNA from a 200 μl sample. Input sample volumes can vary from 50 μl to 1 ml. The method uses a simple genomic DNA purification protocol that uses chaotropic agents to extract DNA from blood cells, denature protein components, and promote the selective binding of DNA to a column-based, novel silica-membrane. The elution volume can be modified as necessary to obtain the appropriate genomic DNA concentration for most downstream molecular biological applications. The kit contains spin columns prepacked with a novel silica membrane, lyophilized proteinase K powder, lysis solution, wash and elution buffers, microcentrifuge collection tubes, a full protocol booklet, and a detachable, quick reference protocol card.

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Digestion of purified genomic DNA with restriction enzymes. Purified genomic DNA from the blood genomicPrep Mini Spin Kit was digested with AluI, EcoRI, HindIII, and BamHI restriction enzymes.

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Kit compatibility across multiple anticoagulants. Isolation of genomic DNA was carried out from 200 μl of human (Hu) whole blood treated with K3-EDTA (EDTA), sodium citrate (Cit) and sodium heparin (Hep). The plot shows mean values for yield and purity with standard deviations.

TECHNICAL SPECIFICATIONS
Yield 4 to 6 μg/200 μl whole blood 
Purity  > 1.7 to 1.6 
Total time of prep* less than 20 min 
Hands-on time* less than 5 min 
Size > 20 kbp 
*including lysis, purification & desalting

References

  1. Sambrook, J., Fritsch, E.F and Maniatis, T. Molecular cloning: A laboratory Manual, Cold Spring Harbor laboratory, 2nd eds., (1989).
  2. Vogelstein, B. and Gillespie, D. Proc. Natl. Acad. Sci. USA 76, 615 (1979).
  3. Marko, M.A., Chipperfield, R. and Birnboim, H.C. Anal. Biochem. 121, 382 (1982).
  4. Voo, K.S. and Jacobsen B.M., Biotechniques 24, 240-243 (1998).
  5. Hilz, H. et al. Eur. J. Biochem. 56, 103-108 (1975).
  6. Ausubel, F.M. et al., eds., Current Protocols in Molecular Biology 1, 1.68 (1991).
  7. Melzak, K. A. et al., J. Coll. Interf. Sci. 181, 635-644 (1996).
فروشنده: آزمیران
گارانتی اصالت و سلامت کالا
پشتیبانی ۷ روز هفته ۲۴ ساعته
۴۰۰,۰۰۰ تومان
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