I. Technological processes

Primer design synthesis

Sample RNA extraction and its quality detection

Sample cDNA synthesis (reverse transcription)

Real-time quantitative PCR of gradient dilution standard and housekeeping gene of sample to be tested

Preparation of DNA templates for mapping gradient dilution standard curves

The samples to be tested of real-time quantitative PCR

II. Contents and criteria for reporting

Experimental reports in detail, including experimental methods, steps, reagents used, instruments, photographs and relevant analytical data.

III. Fees and Service Cycles 

Rates and service cycles vary depending on the sample provided by the customer ,Please contact Customer Service Officer for details or refer to the signed cooperation contract 

IV. Quality assurance

Primer and template binding specificity of Pre-test detection，experimental conditions of optimization,ensure the accuracy of the results through strict QC. 

V. After-sales service

The company will conduct customer visits on a regular basis to improve our service quality. The terms and conditions are governed by the contract of cooperation concluded and the details will vary according to the content of the contract.