Different grades and packaging are available.

ATP, short for Adenosine-5'-triphosphate, is an essential component of energy conversion in biological systems and can be used in a variety of related applications in molecular biology, such as kinase reactions, in vitro transcription, linking and phosphorylation. This product is an ATP sodium saline solution with purity ≥96% (HPLC) with a concentration of 10mM±2mM and is free from endonuclease, exonuclease and ribonuclease contamination. ATP processes are strictly controlled to ensure the end products free from impurities following the Pharmaceutical Manufacturing Guidelines. We guarantee the manufacturing and quality control comply with GMP regulation for tracking each and every step of the manufacturing process, including raw material sourcing. This product has passed the HALAL certification.

10×Transcription Buffer, GMP Grade is the reaction buffer for T7 RNA Polymerase 2.0. This buffer has been optimized to produce 150-250μg of RNA in one reaction. It is also suitable for co-transcription systems, and the co-transcription capping effciency is greater than 95%. The synthesized RNA can be used for downstream applications such as RNA structure and function research, RNase protection, probe hybridization, RNAi, microinjection, and in vitro translation. 10×Transcription Buffer processes are strictly controlled to ensure the end products free from impurities following the Pharmaceutical Manufacturing Guidelines. We guarantee the manufacturing and quality control comply with GMP regulation for tracking each and every step of the manufacturing process, including raw material sourcing.

E. coli Poly (A) Polymerase does not depend on the presence of template, and can catalyze the sequential incorporation of ATP in the form of AMP into the 3´ terminal of RNA, i.e., the addition of polyA tail to the 3´ terminal of RNA. Poly (A) polymerase has A high tail adding efficiency and can add 20 to 200 A bases to the 3´ terminal of RNA. Polyadenylation improves the stability of RNA in cells and enhances the expression efficiency of RNA after transfection or microinjection. Poly(A) tails can be used as primer binding sites for first-strand cDNA synthesis in some applications and can be used for end-labeling or quantification of miRNA. The original enzymes of T7 RNA Transcription Enzyme Mix produced in E. coli. Our manufacturing processes are strictly controlled to ensure the end products free from host protein or nucleic acid contaminations and other impurities following the Pharmaceutical Manufacturing Guidelines. We guarantee the manufacturing and quality control comply with GMP regulation for tracking each and every step of the manufacturing process, including raw material sourcing.