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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.
RNase H is a ribonuclease enzyme that specifically hydrolyzes RNA phosphodiester bonds in DNA-RNA-binding chains. RNase H has a bivalent metal ion catalytic mechanism, such as Mg2+ and Mn2+ directly involved in the catalytic function. RNase H cannot hydrolyze phosphodiester bonds in single- or double-stranded DNA or RNA. This kit can be used to remove mRNA from the DNA and mRNA complex structures before the second strand of cDNA is synthesized, and to achieve pairing through complementary DNA sequences Spot-point snipping of RNA, identification of DNA-RNA hybrids, removal of poly(A) from mRNA hybridization onto poly (dT), In vitro polyadenylation reaction product studies.
Store at -20 °C.