Q1: How many times can it be reused?
Pre-installed desalination column (gravity/centrifugal), gentle operation, no loss, no contamination of glue, can be used dozens of times
Q2: Product recovery rate
Separate the volume as per regulations, with a recovery rate of over 90%
Q3: Can it be used to separate viruses and disinfectant samples?
Theoretically, it's possible, but it hasn't been verified
Q4: What should be done when the sample volume exceeds the maximum loading volume?
If the maximum quantity cannot be exceeded, multiple sample additions are required, with replacement buffer solutions added at intervals.
Q5: Is there a molecular weight cut-off threshold?
It is suitable to use globulins with a molecular weight greater than 5Kd for desalination
Q6: Operational questions
no
Q7: It can be reused several times
It can be reused several times
Q8: Product recovery rate
Product recovery rate
Q9: Can it be used to separate virus and disinfectant samples
Can it be used to separate virus and disinfectant samples
Q10: What should be done when the sample volume is greater than the maximum loading volume
What should be done when the sample volume is greater than the maximum loading volume
Q11: Is there a threshold for molecular weight cut-off
Is there a threshold for molecular weight cut-off
Q12: What does the actual product look like?
Frequently Asked Questions Images and Tables/Images 6.png; Common question pictures and tables
Q13: What is the principle of the desalting column?
Its working principle mainly utilizes the function of molecular sieves to separate substances based on the different molecular sizes of the substances to be separated. After the sample enters the centrifugal desalination column, molecules larger than the maximum pore size of the matrix cannot enter the matrix gel. They move along the gaps between the matrix gel particles with the flowing solution at a relatively fast downward speed and are eluted from the column first. Molecules smaller than the pore size of the matrix will continuously enter the interior of the matrix gel pore size. Therefore, small-molecular-weight substances stay in the matrix for a longer time and move down more slowly, and are eluted after large-molecular-weight substances