1. You've never ever talked to my partner and you don't have any knowledge about the partner, as we don't even really work together too much anymore
2. I was never ever in my life in the UK.
3. I did not ever post a picture of any mass spectrometer on this forum. You probably have one chromosome extra, but well, I'll take my time with you.
4. The pictures were posted by xupc, who contacted me regarding the testing.
5. It's not a mass spec, not like uneducated prick like you would ever know the difference.
6. He literally posted "It should be noted that the spectofotometry machine outputs blinking numbers (they look like this http://chemwiki.ucdavis.edu/@api/deki/files/8472/Spc20Blnk.gif) that you"
So the guy posts AN EXAMPLE MACHINE FROM WIKIPEDIA. A PICTURE OF EXAMPLE OF SPECTROPHOTOMETRIC MACHINE - SO YOU CAN SEE IT FIRST TIME IN YOUR LIFE.
LITERALLY THE FIRST PICTURE THAT GOOGLE PROBABLY SPAT OUT.
7. CBS (cretinous bullshit spammer) and JIM think that's my lab WHILE IT WAS NEVER STATED SO BY ANYBODY BUT HIM AND JIM. It takes a special kind of retard to think that and to think that my lab is on wikipedia, haha.
8. ALSO, Cretinous Bullshit Spammer proves he is retarded again in this mere post:
UK GENTECH LABS where he shows he is even uncabable of understanding the DATE system.
9. I don't think I have to add I was never associated with the lab and never supported it, just stood past my results. If anybody can find anywhere where I shilled for this lab I'll send him a cookie.
There are also other GEMS to be found in that thread from JIM, like:
"Sorry mate but although PHOTOSPEC or GS/MS are quite useful to identify sample compounds NONE are capable of sample QUANTIFICATION!" - no comment, just lol
"You just can't slam all that crap into a Spec and obtain results, the constituents MUST first be isolated into individual compounds and then run SEPARATELY." - he seems to no have ever heard of chromatography being a separation technique, haha
"If you just run an oil with the BA, NaB, Tren-A and a monoglyceride in a MS the fragments will form dimers trimers and sodium adducts for sure. Now that's excluding any other adulterants EVERY UGL uses in their formulation.
How odd is it NO sodium adducts or adulterants were detected, only those substances that were likely listed on the vial labeling.." - sodium in oils? where exactly? you put table salt in your injectables JIM? that would explain a lot of stuff going on with your brain
Chemistry 101, failed again by JIM.
Do you want me to quote him in another thread, where he says the MS is awesome for quantitation?
Or do you want me to quote you about 500000 publications from REAL SCIENTISTS unlike JIM, who USE MS for Uv/VIS for quantitation?
Come at this you little a-hole, I'll enjoy it.
It's cool that you got a pic with JIM, which one it who?
See up, little doggie.
Try forming a coherent sentence you uneducated fuck.
What you wrote is mess both gramatically both factually and has no basis in truth.
Forming coherent sentences is kinda a requirement to get into and pass the med school, which again makes me wonder...
I'll make a thread saying you are dickless... And don't you dare to post there! If you disagree measure your dick by YOURSELF and START A NEW THREAD. Or better off LEAVE.
>5 hplcs
JIM being at it in maths again.
Also your evidence... I don't know, it kinda lacks the 'evidence' part.
Also MY LINE WAS NOT BAD DATA. I am not as retarded to claim that without ANY EVIDENCE - SOMETHING WHAT YOU DO ALL THE TIME (which makes you a retard I guess?).
My line is that you are a liar and an uneducated ass.
Something for you, Mr. JIM again, as you keep forgetting to respond to this:
"Generic" GH ASSAYS
"Generic" GH ASSAYS
"Generic" GH ASSAYS
Also, the HPLC is brand new, thank you.
Sorry, can't hear you, just got off the phone with Mr. President.
He cries in his sleep because of that?