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On-Column DNase Digestion Assay Kit
A quick and efficient way to remove contaminating genomic DNA from RNA preparations.
By: BioVision, Inc.
Figure 1: 5 μg Jurkat cell RNA mixed with Hind III-digested λ DNA was purified. 1. RNA without DNase treatment. 2. DNase treatment prior to the RNA Clean-Up Protocol. 3. RNA Clean-Up Protocol with optional On-Column DNA digestion step. RM: Riboruler marker. All
samples were incubated at RT for 30 min for DNase treatment. 10 μl was loaded per lane.
Figure 2: RNA was purified from Jurkat cells using BV Cat# K2065. Lanes 1 & 3. RNA without DNase treatment. Lanes 2 & 4. RNA with DNase treatment. RM: Riboruler marker. All samples were incubated at RT for 15 min for DNase treatment. 10 μl of elution was loaded per lane.
For more information on this Assay kit Cat# K2066, Visit: https://bit.ly/
(408) 493-1800 EXt: 224