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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.
DNase I is a deoxyribonucleic acid endonuclease that hydrolyzes single- or double-stranded DNA, producing dinucleotide, trinucleotide, and oligonucleotide products with 3’-hydroxyl and 5’-phosphate group ends. The activity of DNase I is Ca2+ dependent and can be activated by either Mg2+ or Mn2+. In the presence of Mg2+, DNase I can randomly cleave any site of double-stranded DNA. In the presence of Mn2+, DNase I recognizes both strands of DNA simultaneously and cleaves them at nearly identical sites.
DNase I can act on single-stranded DNA, double-stranded DNA, chromatin, and RNA:DNA hybrids. It is suitable for RNA extraction, in vitro transcription, and DNA removal in RT-PCR experiments. The production process of this product strictly controls host protein residues, nucleic acid residues, etc., and conforms to GMP production and quality management standards.
Store the components at -20°C.