I am using Qiagen Blood RNA Mini kit to isolate RNA from whole blood.. and the A260/A230 is quite low, even below 1. My main downstream application is RNA-seq. and I am not sure if this low ratio would affect the sequencing.
is low A260/A230 due to low concentration of RNA 20-50 ng/μL), presence of EDTA in the blood samples, or buffer carryover? how can I improve this ratio?