Skip to main content
Sitemap
|
Contact us
Facebook
Twitter
YouTube
Home
About Us
Introduction
Quality Policy
Accreditation
Publications
Products
New
Download
Plasmid DNA
Post Reaction DNA
Genomic DNA
Total RNA
DNA RNA Protein
Virus DNA/RNA
Magnetic Beads
DNA Ladders
Enzymes
PCR
Protein
Vacuum Filtration
Catalogue
Q&A
Plasmid DNA
Gel/PCR
Genomic DNA
RNA
Blog
Home
About Us
Introduction
Quality Policy
Accreditation
Publications
Products
New
Download
Q&A
Plasmid DNA
Gel/PCR
Genomic DNA
RNA
Blog
Q&A
Product support
Plasmid DNA
Gel/PCR
Genomic DNA
RNA
Genomic DNA
Breadcrumb
Frequently Asked Questions
Genomic DNA
What should be done if the column is clogged?
Why is the DNA recovery lower than expected?
Why doesn't the Eluted DNA perform well in downstream applications?
Why does the genomic DNA band appear smeared in agarose gel electrophoresis?
What is the key to successfully isolating genomic DNA of good yield and quality?
Why does the sample appear viscous after sample Lysis and not pass through the column easily, even when less than the suggested maximum sample amount is used?
When Buffy coat is used, the column tends to be clogged.