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In vitro transcription of capped mRNA with modified nucleotides and Poly(A) tail
TSA (Tyramide Signal Amplification), used for signal amplification of ISH, IHC and IC etc.
Separation of phosphorylated and non-phosphorylated proteins without phospho-specific antibody
A convenient and sensitive way for cell proliferation assay and cytotoxicity assay
Protect the integrity of proteins from multiple proteases and phosphatases for different applications.
The kit uses magnetic bead purification for rapid sorting and recovery of DNA fragment size in high-throughput sequencing library (NGS) construction. The binding buffer of the kit contains superparamagnetic beads, which selectively bind DNA fragments based on the volume ratio of the bead suspension to the sample. High-purity DNA fragments eluted by magnetic separation and ethanol wash, low-salt elution buffer, or nuclease-free water are free of contaminants such as nucleotides, primers, linkers, enzymes, and salts, and can be used directly in downstream applications such as digestion, sequencing, hybridization, PCR, and more. Can be applied to manual or automatic liquid handling equipment.
The product is compatible with various brands of DNA and RNA library preparation kits and the library preparation process reported in the literature and is exactly the same as the widely used AMPure XP Beads, and the yield and size distribution of the library are highly consistent with AMPure XP Beads, so it can seamlessly replace AMPure XP Beads and effectively reduce your library construction cost.