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hobglobin

Member Since 26 Jan 2009
Offline Last Active Today, 12:47 PM
*****

#125925 Words, Words, Words

Posted hobglobin on 22 December 2011 - 12:26 PM

junk food

but I guess the pure alcohol bottle from your lab closet is disappearing on Fridays faster than usual, eh? Posted Image


#125202 Need help for PCR for AT rich gene

Posted hobglobin on 10 December 2011 - 11:05 AM

Often it is suggested to use betaine to make a PCR work in AT-rich regions. Also the companies say this about their additives (Q-solution (= betaine), PCRx Enhancer Solution etc). No idea if it's true, but an attempt might be useful.


#122978 Self-plagiarism?

Posted hobglobin on 03 November 2011 - 08:47 AM

What do you mean with "the chapter" of your thesis? Anyway if it's one chapter of several it should be okay, because an undergrad study can be a good starting point of a phd thesis. But it shouldn't be too much (the extent of repetition is critical here) and it anyway makes not much sense to do the same work again??


#121883 I was plagiarized, what should I do?

Posted hobglobin on 19 October 2011 - 08:12 AM

also as decent researcher you need as many papers as possible and poster publications help too...therefore I'd insist on my rights here...


#121229 salts in PCR

Posted hobglobin on 10 October 2011 - 08:36 AM

Cations stabilize the duplex state of DNA, and the algorithms for salt correction formulas are developed using Na+concentrations, for whatever reasons. So I'd take into account monovalent and bivalent ions as primer3 does it. I guess it's not that important if it's K+ or Na+ (someone might correct me here).
NH4+ surely also will have an effect as it is a cation, but it also influences the enzyme's activity. I don't know any program that accounts for that, but perhaps no data are available, as such additives are anyway a trial and error issue.
Actually my way to deal with it is to calculate roughly an annealing temperature (using standard settings) and then later doing a gradient PCR, if the reaction works. The calculated Tms are also always an estimate that have to be verified and then optimised. And also with simple formulas such as
Tm (°C) = 81.5 + 0.41(%GC) - (675/N) or Tm = 4(G + C) + 2(A + T) °C PCRs worked...Posted Image


#118904 an alternative way for money

Posted hobglobin on 04 September 2011 - 02:14 AM

Writing proposals, outlines for grants and projects is a tiresome duty if you want to stay in research and have no permanent position or need additional money for a project....
as an alternative way to get money crowd funding becomes more and more important, and next to websites where this is offered for all types of projects, also sites that are only for funding science projects are created.
Here is a short paper about this in Nature Neuroscience.

A few examples:

Kickstarter is a website for all kinds of projects and ideas that need money (arts projects, start up companies, etc)

Fundscience (non-profit, USA-based, only for science projects)

MyProjects (UK, only for cancer research projects)

Open Genius (non-profit, science only, still in development I think)

Because of the not that high amounts of money you can get, it's perhaps a good idea for pilot projects, feasibility studies or funding gaps. Have a look.


#118223 Friday, I'm in love

Posted hobglobin on 25 August 2011 - 11:48 AM

And here an adapted version of an old song from Alice Cooper: School's Out

Well we're not choosy
All the nerds and geeks
bein' all that nosey
'Cause they found no sheiks
Well they can't fund ya
Can't find work
If that don't suit ya
Try to smirk

Lab's out for summer
Lab's out forever
Lab's been blown to pieces

No more pipets
No more papers
No more student’s dirty coats

Well we got no class
And we got no results
And we got no publication
We can't even think of a word that rhymes

Lab's out for summer
Lab's out forever
Lab's been blown to pieces

No more enzymes
No more digests
No more technician's dirty coats

Out for summer
Out till fall
We might not go back at all

Lab's out forever
Lab's out for summer
Lab's out with fever
Lab's out completely

Posted Image


#116984 experiments in progress

Posted hobglobin on 09 August 2011 - 09:01 AM

Posted Image


#114381 How to open *.bin?

Posted hobglobin on 06 July 2011 - 08:46 AM

View Postpito, on 06 July 2011 - 07:12 AM, said:

you need isobuster for it.
http://www.smart-pro...terdownload.php

and maybe this will help too:
http://www.ehow.com/...n-bin-file.html
But only if it's a disc image (then it's presumably a large file). But it can also be a file with general binary code (see your windows system folder). Or a data file that stored data as binary code (some population genetics software has it as results output). For these files I'd use an editor (results) or hexeditor (binary file, here you might get an idea which program produced this file)....QuickView Plus, hexedit, notepad would be my ideas.


#110281 Musca domestica gDNA isolation

Posted hobglobin on 19 May 2011 - 10:56 AM

RNA? There can be surprisingly much and large in insects. Add RNAse and see if the band is still there.


#110081 Micropipetting technique

Posted hobglobin on 17 May 2011 - 09:02 AM

using a balance to control pipetting was suggested several times before

here is a powerpoint presentation from Rainin with several hints and some good advice:

Attached File  raininpipettetechniques.ppt   1.83MB   164 downloads


#107851 Words, Words, Words

Posted hobglobin on 24 April 2011 - 12:45 PM

nice theory


why doesn't it matter? and next week I'll diet I guess... :P


#106241 Nanodrop DNA

Posted hobglobin on 08 April 2011 - 12:01 PM

Read this too:
Link


#103867 Placing dNTP in 64 C waterbath

Posted hobglobin on 16 March 2011 - 10:31 AM

I never did it, but don't think it will ruin it. The PCR reaction has higher temperatures...
Of course it depends on the time there, storing it at that temp will be harmful of course.  ;)


#100823 Casting 3% agarose

Posted hobglobin on 16 February 2011 - 07:07 AM

If it's not the too hot temperature itself causing the cracks, but the temperature differences between hot gel and cold tray (leading to tensions within the tray material), you might preheat the tray slowly e.g. in a water bath.




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