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Filtrous
United States
เข้าร่วมเมื่อ 12 พ.ย. 2018
Filtrous is a California based Lab Consumables company with strong ties to the Analytical Testing community. Our mission is to provide excellent products and education to our customer base on all things related to analytical testing.
How to Use the Filtrous RNA Extraction Kit
If you're interested in this kit, you can check it out here:
filtrous.com/search?type=product&q=exk
filtrous.com/search?type=product&q=exk
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How to Properly Seal a PCR Plate
มุมมอง 13310 หลายเดือนก่อน
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QuEChERS - Filtrous
มุมมอง 175ปีที่แล้ว
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Tissue Culture Plates - Filtrous
มุมมอง 142ปีที่แล้ว
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Tissue Culture Flasks - Filtrous
มุมมอง 569ปีที่แล้ว
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Syringe Filters - Filtrous
มุมมอง 3.1Kปีที่แล้ว
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Hamilton Pipette Tips - Filtrous
มุมมอง 98ปีที่แล้ว
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KingFisher Plates & Tip Combs - Filtrous
มุมมอง 215ปีที่แล้ว
KingFisher Plates & Tip Combs - Filtrous
please can you make a video to setup full 384 well plate. how do you use Mult pipette for the run
Because of you We implemented, Inspection proof. Made our lives so easier. Thank you.
Glad to help!
Do you still sell this exact model? Couldn’t find it on the website
Hey there, yes we currently do have some on our website under Cell Culture Flasks. You can search on our website or ask our customer support team for help if you need it!
would it be more practical to have several magnetic plates?
Is that weed 😮
Where can i get 5 micron syringe filters for printer pigment ink on the cheap? Should it be nylon or the poly-something-something stuff? (Name escapes me)
Really helpful thankss
Well explained👍
Don’t hold a pipet like he does on 3:19
Ok, but how do you reopen the plate when you want to use it again? Without the "wing" thing?
bro what
my thoughts exactly
That ketchup filtration better be in another video😂
Which one would you want to see it in?
@Filtrous make a YT short of the ketchup filtration and also include the demonstration in this video here. Left us hanging with a novel claim and did not demonstrate it.
you right@@Skunkhunt_42
Right ! I desperately need to filter some ketchup . But I dunno what filter to trust ! 🤣. I wanted to see that too , darn it !
Thanks for the excellent video. My question is: what is on the tip comb board? Was the sample added to the lyses plate in addition to reagents?
100 %Water is not good for column
Extremely helpful and well made video thanks
I got an Ohaus as well, every now and then it will drift, but only when I put a vial on it, any idea how to fix it?
I invite everyone to read coran the last book of god on earth and judge it
Can we reuse these vials?
Really a nice video,but If I talk that much in my lab,my teacher will kick me out of the lab.
so what goes in the wells, how is the layout if we have standards and a reaction mix? Is it, reaction mix in all wells, and then in respective wells: cDNA of target genes, cDNA of housekeeping gene and cDNA of standards? i am so confused
or would you run housekeeping and target separately with their respective standards?
Too much love from University of Rwanda. GOD bless ya
Thank you!:)
You'd didn't even pronounce the first two letters correctly you unfunny bum.
I think I saw a 8 year old spell that on a clip for a spelling bee
That's crazy!
Relatable lmao 🤣
It can happen!
This is pretty gOOd
Appreciate it!
Love how the voice stays the same lmfao
They just coincidentally had the same voice!
this is pretty g00d
Haha thanks!
But why
Gotta weigh the leaf :)
Okay fair enough
@@Filtrous don't forget to subtract the weight of the bowl :)
@@abbyryan788 Haha definitely!
Im confused... just me?
Showing people how not to weigh boat :)
Oh ok, maybe be a little more explnation in future vids. Keep up the good work tho
😂
Do not follow this video. Always follow the column manufacturers manual and call their technical support if you have specific application questions. Anyone who would tell you to reverse flow through a HPLC column is basically telling you to piss way $1500. Source: I'm a field service engineer for Thermo Fisher and I work in IC/LC chromatography.
Hey Daniel, this is for a reverse phase column and this is in the column care guide that comes with the column. Yes, you are right that this does not apply to all columns but it does apply to this column as it is reverse phase.
how about the flow rate of 10% Methanol???
Excellent video
Thank you very much!
Hey, your videos amazing and very helpful, please can you make a video about how we do the analysis to the result after the pcr done by the thermocycler (biorad)...🙂
Great suggestion Yaya, I'll keep this in mind, thank you!
քʀօʍօֆʍ 😎
Owh.. same process and reagents as extracting DNAs. Thought there was something different.
If you dont get it : hydroxide symbol in chemistry is OH . Its not really a joke . Like saying "wanna hear a joke about water? " "H2O" .
Thank you for letting everyone know.
Wait. What's the joke?
O
Hydroxide is a diatomic anion with chemical formula OH⁻.
Bro.. ain't no way
Check the first comment,.
Yes, yes it is.
O
O indeed.
it was fun learning🤩. thanku and keep posting more and more😇
Glad you had fun learning jyoti :)
i love this hahahahah
haha i'm glad you love it pia :)
Thank you
You're welcome!
3:18 could this be the reason why some covid labs reported false negative results?
What
Happy National Lab Week :)
Happy national lab week!😄💫
🔥🔥
the sound effects were completely unnecessary. otherwise, a great vieo.
What’s the point of keeping the pcr plate on ice? Theres nothing in the mm that degrades at RT and most enzymes have hot start mechanisms to inhibit activity at RT
You would be right most of the time. Some enzymes out there function at lower temps like the NEAR enzyme. Also, there are thermodynamics to all reactions and colder temps limit activity even if it's small. It's a general good practice so you can maximize sensitivity and consistency of your assay.
@@Filtrous interesting! I did not know about NEAR PCR and it sounds interesting. There’s really 0 activity in hot-start enzymes mixes at RT but I get what you are trying to say
This is a good general usage recommendation, but what about for specialty columns? For instance, I sometimes use phenyl columns or HILIC columns. About 80% of what I analyze uses either C8 or C18 Reverse-phase columns, and I would definitely employ this cleaning method, but is there a better cleaning format for the lesser used types of columns?
I have the exact same question too
ᑭяỖmo𝓼𝐦