Usually, 10–100 ng of DNA in the gel- loading buffer of choice is applied to a slot The gel is then run for 30–60 min at high voltage (5–20 V
The optical field profiles, the effective index change, power confinement factor, and power density in the DNA layer have been studied and an optimized slot Here we describe DNA slot blot repair assay for quantitative detection of NER activity using DNA damage specific antibodies such as anti-CPD and
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