QIAGEN RNase-Free DNase Set保证无RNA酶、经严格质控和优化,配合RNeasy操作流程和QIAamp RNA Blood Mini操作流程使用。一般来说,使用RNeasy Kits纯化RNA时,不需要DNA酶消化步骤,因为硅胶膜离心柱技术可有效地去除大部分DNA,而无需DNA酶处理。然而,某些RNA应用对痕量DNA非常敏感,因此需要*去除DNA。QIAGEN RNase-Free DNase Set中提供RDD缓冲液,经优化可用于柱上DNA酶消化。该缓冲液也非常适合于溶液中高效DNA酶消化。在使用RNeasy试剂盒和QIAamp RNA Blood Mini Kit从细胞和组织中纯化RNA的过程中,QIAGEN RNase-Free DNase Set提供高效的柱上DNA消化。后续的洗涤步骤可将DNA酶高效去除。当使用RNeasy 96 试剂盒过程中需要DNA酶处理时,请QIAGEN Technical Services或当地经销商获取专门优化的实验方案。QIAGEN RNase-Free DNase Set是以稳定的、冻干粉酶形式提供。QIAGEN RNase-Free DNase Set提供1500 Kunitz units。1 Kunitz units是指在25°C、pH 5.0条件下,以高度聚合的DNA为底物,使每毫升底物的A260值每分钟升高0.001时所需要的DNase I的量(Kunitz, M. [1950] Crystalline desoxyribonuclease. I. Isolation and general properties, spectrophotometric method for the measurement of desoxyribonuclease activity. II. Digestion of thymus nucleic acid (desoxyribonucleic acid): the kinetics of the reaction. J. Gen. Physiol. 33, 349 and 363)。
订购信息:
Cat No./ID: 79254
RNase-Free DNase Set (50)
1500 Kunitz units RNase-free DNase I, RNase-free Buffer RDD, and RNase-free water for 50 RNA minipreps
The MagMAX™ Cell-Free DNA Isolation Kit is designed for enrichment of circulating cell-free DNA (cfDNA) and optimized for use with biological samples such as serum and plasma. The kit is based on MagMAX™ magnetic-bead technology, enabling reproducible recovery of high-quality DNA that is suitable for a broad range of applications, including real-time PCR, digital PCR, and next-generation sequencing.
Scalable isolation of circulating nucleic acid from plasma, serum, and urine cfDNA recovery is challenging due to the limited amount present in cell-free samples. The MagMAX Cell-Free DNA Isolation Kit addresses this with its magnetic bead-based purification format which allows you to easily process a wide range of sample input volumes, from 500 µL to 10 mL. When used with either a KingFisher™ Duo Prime or KingFisher™ Flex magnetic particle processor, 6 to 24 plasma/serum samples of 2 mL input volume can be isolated at once. Alternatively, samples can be processed manually with the use of a magnetic stand.
Features of the MagMAX Cell-Free DNA Isolation Kit include:
• Flexible design that permits both manual and automated isolation of cfDNA • Scalable format that allows for higher and lower input volumes • Automation-ready, phenol-free extraction • Fast procedure, which allows 6 to 24 samples to be processed typically in 40 minutes or less when used with the KingFisher Duo Prime Magnetic Particle Processor or the KingFisher Flex Magnetic Particle Processor with a 24 Deep-Well Head • Wide sample volume inputs range from 500 µL to 10 mL of plasma/serum or urine • Contains Dynabeads™ MyOne™ Silane for consistent isolation of cfDNA • Elution volumes range from 15 µL to 50 µL
1) E. Hochuli, H. Doeli and A. Schacher, "New Metal Chelate Adsorbent Selective for Proteins and Peptides Containing Neighbouring Histidine Residues", J. Chromatogr., 1987, 411, 177. 2) E. Hochuli, "Large-scale Chromatography of Recombinant Proteins", J. Chromatogr., 1988, 444, 293. 3) 河田聡, 高木俊夫, "表面プラズモン共鳴センサとは", 蛋白質、核酸、酵素, 1992, 37(15), 3005. 4) 笠井献一, "表面プラズモン共鳴(SPR)を利用したバイオセンサー", 蛋白質、核酸、酵素, 1992, 37(15), 2977. 5) Y. C. Sasaki, Y. Suzuki and T. Ishibashi, "Fluorescent X-ray Interference from a Protein Monolayer", Science, 1994, 263, 62. 6) G. B. Sigal, C. Bamdad, A. Barberis, J. Strominger and G. M. Whitesides, "A Self-assembled Monolayer for the Binding and Study of Histidine-tagged Proteins by Surface Plasmon Resonance”, Anal. Chem., 1996, 68, 490. 7) E. L. Schmid, T. A. Keller, Z. Dienes and H. Vogel, "Reversible Oriented Surface Immobilization of Functional Proteins on Oxide Surface", Anal. Chem., 1997, 69, 1979. 8) 橋本せつ子, "表面プラズモン共鳴現象を利用する生体分子相互作用の解析", ぶんせき, 1997, 362. 9) R. Yasuda, H. Noji, K. Kinosita and M. Yoshida, "F1-ATPase is a Highly Efficient Molecular Motor that Rotates with Discrete 120°Steps", Cell, 1998, 93, 1117.