S. cerevisiae Host Cell DNA Residue Detection Kit is used for the quantitative analysis of S. cerevisiae host cell DNA residuce in intermediate samples, semi-finished and finished products of various biological products. This kit adopts Taqman fluorescent probe and the polymerase chain reaction (PCR) method, which has fg level minimum detection limit and can specifically and quickly detect the residual S. cerevisiae cell DNA. The kit needs to be used together with the the Residual DNA Sample Preparation Kit (Cat# 18461ES). Feature Compliance with regulations: the products are fully validated according to the requirements of Chp, USP, ICH, etc., and their performance is in line with Chinese and foreign regulations and standards; Guarantee of quality: the raw materials of the kits are all self-developed, and the qPCR Mix and other enzyme products are produced in an ultra-clean enzyme factory; High sensitivity: the limit of quantification can reach 3 fg/μL level; High precision: high intra-batch repeatability and low inter-batch variation; Strong exclusivity: specific detection of residual DNA in S. cerevisiae cells without interference from other exogenous genomic DNA; Strong anti-interference: add internal control (IC), easy to exclude sample interference, reaction preparation abnormalities and other factors. Application Residual S. cerevisiae Host Cell DNA test in biological products. Specification Sensitivity 3 fg/μL (range 30fg/μL~300pg/μL) Assay Time ~1.5 hours Assay Principle Fluorescent probe qPCR method Required Instruments Real-time fluorescence quantitative PCR system Components Components No. Name 41324ES50-EN 41324ES60-EN 41324-A S. cerevisiae qPCR Mix 0.75 mL 1.5 mL 41324-B S. cerevisiae Primer&Probe Mix 200 μL 400 μL 41324-C DNA Dilution Buffer 1.8 mL×2 1.8 mL×4 41324-D S. cerevisiae DNA Control (30 ng/μL) 25 μL 50 μL 41324-E IC* 50 μL 100 μL *IC：Internal control. Figures Limit of quantification S. cerevisiae DNA was detected at 30 fg/uL, 10 fg/uL, 3 fg/uL, and 1 fg/uL with 10 replicates for each concentration. The results showed that at concentrations of 3 fg/uL and above, the CV was
