Hi, anybody here currently working with the new Hydroshear Plus form Digilab? I am in a big problem here!
Unconfigured Ad
Collapse
X
-
-
hydroshear plus
i have followed as instructed in the manual. the same speed code & cycle. however, the syringe broke 2 times already. after changing the syringe, i successfully perform the shearing. when i wanted to repeat the shearing, i notice there is white precipitate inside the syringe. now i don't know what should i do. and i think the syringe broken again.
Comment
-
-
Hope you managed to solve your problem in the meantime, but if not...
Do you wash the system often enough between and after shearing with filtered solutions (water, HCl, NaOH)?
Did you make sure your shearing assembly is not clogged? Look at the assembly under a microscope to make sure it is not clogged or damaged; in any case try washing it by putting in a sonicating water bath with distilled water or a weak SDS solution.
To make sure your assembly does not get clogged, make sure your DNA is super pure! The white precipitate could possibly be salt. Do a buffer exchange with columns or other purification means! If there are particles in your DNA sample or the DNA is not completely solubilized, it can clog the shearing assembly.
If the assembly is clogged the syringe can break.
We've only managed to clog the shearing assembly so far, but we've noticed it on time (leaking) and then washed it. No problems occurred after that.
It might be that your shearing assembly was clogged but you kept on shearing and the syringe broke.
Try contacting the Digilab technical support as well for more info!
Comment
-
Latest Articles
Collapse
-
by SEQadmin2
I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
Here are nine questions we think about, in roughly the order they matter, before...-
Channel: Articles
06-18-2026, 07:11 AM -
-
by SEQadmin2
Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.
The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
...-
Channel: Articles
06-02-2026, 10:05 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Whole-Genome Sequencing Traces Faroe Islands Ancestry to a North Atlantic Founder Population
by SEQadmin2
Started by SEQadmin2, 06-17-2026, 06:09 AM
|
0 responses
25 views
0 reactions
|
Last Post
by SEQadmin2
06-17-2026, 06:09 AM
|
||
|
Sequencing the Two-Toed Sloth Genome Reveals Jumping Genes Tied to Its Extreme Metabolism
by SEQadmin2
Started by SEQadmin2, 06-09-2026, 11:58 AM
|
0 responses
42 views
0 reactions
|
Last Post
by SEQadmin2
06-09-2026, 11:58 AM
|
||
|
Started by SEQadmin2, 06-05-2026, 10:09 AM
|
0 responses
48 views
0 reactions
|
Last Post
by SEQadmin2
06-05-2026, 10:09 AM
|
||
|
Started by SEQadmin2, 06-04-2026, 08:59 AM
|
0 responses
49 views
0 reactions
|
Last Post
by SEQadmin2
06-04-2026, 08:59 AM
|
Comment