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A highly sensitive telomerase detection method that combines telomefic repeat amplification protocol(TRAP)and magnetic beads based electrochemiluminescence(ECL)assay has been developed.Briefly,telomerase recognizes biotinylated telomerase synthesis primer(B-TS)and synthesizes extension products,which then serve as the templates for PCR amplification using B-TS as the forward primer and tris-(2’2’-bipyddyl)ruthenium(TBR)labeled ACX(TBR-ACX)as the reversed primer.The amplified product is captured on streptavidin-coated paramagnetic beads and detected by ECL.Telomerase positive HeLa cells were used to validate the feasibility of the method.The experimental results showed down to 10 cancer cells can be detected easily.The method is a useful tool for telomerase activity analysis due to its sensitivity,rapidity,safety,high throughput,and low cost.It can be used for screening a large amount of clinical samples.
A highly sensitive telomerase detection method that combines telomefic repeat amplification protocol (TRAP) and magnetic beads based electrochemiluminescence (ECL) assay has been developed. Briefly, telomerase recognizes biotinylated telomerase synthesis primer (B-TS) and synthesizes extension products, which then serve as the templates for PCR amplification using B-TS as the forward primer and tris- (2’2’-bipyddyl) ruthenium (TBR) labeled ACX (TBR-ACX) as the latter primer. amplified product was captured on streptavidin-coated paramagnetic beads and detected by ECL.Telomerase positive HeLa cells were used to validate the feasibility of the method. The experimental results showed down to 10 cancer cells can be detected easily. The method is a useful tool for telomerase activity analysis due to its sensitivity, rapidity , safety, high throughput, and low cost. It can be used for screening a large amount of clinical samples.