How do I remove the bubbles in Agilent Infinity II 1260 series
@kalrbaum.15 күн бұрын
Exactly what i was looking for, thanks!
@BlahBlah-gb6stАй бұрын
What could be wrong if my inlet total flow falls when the oven temp is ramping up? I have changed the septum.
@srirampmna135Ай бұрын
Sir how to calculate the delay time from detector to fraction collection tube .Could u pls share ur ideas ?
@LaLa-qf1qzАй бұрын
You are a great speaker. Very confident and helpful, thank you
@gooddaniel8603Ай бұрын
How do I apply to this class ?
@Ccccccccccsssssssssss2 ай бұрын
Thanks for the great video!
@lucasclementinomourao56772 ай бұрын
I'm currently working on a method where a pair of hydrophilic peaks elutes in less than 5 minutes, while another pair elutes about 15 minutes later in isocratic mode. When I use gradient methods (~50 to 70% ACN), the baseline drift increases significantly. What is the best way to run a gradient in these methods? Should I implement a steep gradient change in less than a minute or use a smoother gradient (over a longer period) ?
@srirampmna1352 ай бұрын
Sir, how does the molecule come.down when we place positive charge repeller .
@srirampmna1352 ай бұрын
Sir, could u pls explain about mass tuning in one video.
@bsadeghi10982 ай бұрын
Thats very great,thanks for these useful points,could you please explain the thermostat and autosampler parts too?how can i understand the effeciency of these two parts
@mohamedislambenghaname1333 ай бұрын
Is there any good method for erythropoietin in albumin serum ?
@denniswhv75463 ай бұрын
wow thanks!
@axionlabs3 ай бұрын
Welcome!
@Will_be_back_by_20243 ай бұрын
I like you! You're very practical
@axionlabs3 ай бұрын
I appreciate that!
@tayyabaraja4333 ай бұрын
Sir can u please tell me... Which type of standards used for the Hplc of The sample of TSB broth inoculated with bacterial strains for growth with crude oil?
@Sarahishamvasileva4 ай бұрын
How i can learn abt calibration, is it available for gcms
@wahmfarad27194 ай бұрын
Dear sir you explained well..
@137bob3d4 ай бұрын
this Axion guy gets my vote for having fab' knowledge at the tip of his tongue
@dewittk94045 ай бұрын
I’ve read that acetonitrile can have amine impurities and form deposits in pump components over time. Is there a procedure for flushing the system to remove/prevent this?
@user-nm4yb7gl5u5 ай бұрын
Great content! Thank u so much for sharing this!!
@axionlabs3 ай бұрын
My pleasure!
@Phasianidaes5 ай бұрын
Great explanation! This is critical when transferring methods into a lab with different brand and models
@axionlabs3 ай бұрын
Yes, exactly
@heboottoobigforhegotdamnfeet5 ай бұрын
How to deal with negative peaks on refractive index?
@MOHDSALEEM-gh7tf5 ай бұрын
Thank you sir for clearing my doubts 😊
@leewilliam34175 ай бұрын
Thanks so much 😊
@axionlabs3 ай бұрын
You're welcome 😊
@marcoromo92525 ай бұрын
how does it work if using an internal standard and using their ratios?
@shreem38595 ай бұрын
Very pocket friendly PI... fellows from this lab will be very lucky
@user-gc1ys5sh8v5 ай бұрын
HI Lee indeed inspiring,
@axionlabs3 ай бұрын
Glad you think so!
@srirampmna1356 ай бұрын
Iam facing issue in gcms as it shows vial out of range.hiw can I fix it
@user-yz8lr6zv4u6 ай бұрын
What HPLC machine is good enough to check Thc potency?
@MrSpicabooo18 күн бұрын
The best right now are waters arcs hplc amd waters acuity uplc
@srirampmna1356 ай бұрын
Can u pls explain how to setup peak purity and threshold in spectra option in agilent
@srirampmna1356 ай бұрын
I wish I could work under u and learn .Ur videos r really informative and interesting
@srirampmna1356 ай бұрын
Couod u please explain how to set the peak purity and threshold in agilent
@srirampmna1356 ай бұрын
I wish I could work under u and learn
@yerielhiciano76356 ай бұрын
What about highly acidic or basic samples? Will that affect the C18 ligands of a column. I work with human serum and plasma that are treated with acid, precipitated and the supernate is injected so not the same as the mobile phase.
@srirampmna1356 ай бұрын
Could u pls explain how to setup peak purity setup in spectra option in agilent
@user-vr6ol2hj3d6 ай бұрын
wow how excellent video ! this video was very helpful for me, but i want to know amount of sample using calibration curve you described
@MrScorpioAngel7 ай бұрын
good cure to learn!
@srirampmna1357 ай бұрын
Thank you soo much explaining and making such informatve video.Looking for more such videos .Can you please do a video on peak purity and independent column compartment port switching in agilent in detail
@rpsly18737 ай бұрын
Excellent explanation, awesome video
@axionlabs3 ай бұрын
Glad you liked it!
@MemoreSPalay7 ай бұрын
Thanks for this knowledge but I have a question Sir. Does pH also affect resolution and how?
@srirampmna1357 ай бұрын
Can u explain how to check whether uv lamp.intensity has reduced or.not?
@srirampmna1357 ай бұрын
I find this video and channel very useful and informative.Super and amazing
@axionlabs3 ай бұрын
Thank you so much 🙂
@srirampmna1357 ай бұрын
Amazing .where is ur lab ?
@axionlabs3 ай бұрын
It's in Chicago. Check out our lab here axionlabs.com/lc-gc-bootcamp/
@kirranaslam60777 ай бұрын
when there is the need of new claibration table then a option of then this table would be deleted??
@nadeemiqbal47427 ай бұрын
Thank you sir.
@andyrieder33457 ай бұрын
I am assuming Courts use the GC method right?
@muhamedhammoud93127 ай бұрын
love the videos, really helped me in my studies, great explanation, thanks!
@MrScorpioAngel9 ай бұрын
always best advices🙂
@MoodysZed9 ай бұрын
Great video. How simple easy and concise!
@axionlabs8 ай бұрын
Glad it was helpful!
@exploiteddna10 ай бұрын
what is the functional difference between running green stainless vs red stainless @ 0.3mL/min (Ion Paired, RP, LCMS). nice vids, thx for sharing