Common questions about nucleic acid extraction and product usage
Current total RNA extraction methods cannot completely remove DNA. Our total RNA kit uses a double-column method that removes most genomic DNA, but trace amounts may remain.
For purer RNA, we recommend:
DNase treatment is not recommended as digestion may be incomplete and may cause RNA degradation.
Storage conditions vary by product:
Orders can be placed through the following channels:
Please include catalog number, product name, quantity, delivery timeline, customer information, payment details, and shipping address with your order.
Upon receiving goods, please immediately inspect:
Do not sign for damaged goods. Contact our headquarters or local distributor immediately. Replacement will be arranged after verification.
Our Gel Extraction Kit recovers DNA fragments from 100bp to 40kb with a recovery rate > 90%. Maximum binding capacity: 10μg (mini column), 40μg (midi column/96-well plate per well).
Yes. This kit is specifically designed for purifying nucleic acid probes <100bp and PCR primers. Tested recovery rate > 90% for 30bp DNA fragments. Uses a novel silica matrix and unique buffer system. Maximum binding capacity: 20μg (mini column), 100μg (midi column/96-well plate).
Our DNA Enrichment Kit is designed for DNA solution concentration, achieving up to 50-fold concentration. It also removes oligonucleotides, primer dimers, and salts, providing simultaneous purification.
Yes, we hold multiple medical device registrations:
These products are suitable for clinical in vitro diagnostic nucleic acid extraction, enrichment, and purification.