mm. Yea, that could be a problem. So the buffer is basically just a conductive gasket.
--A
On Thu, Mar 7, 2013 at 3:10 PM, Nathan McCorkle <nmz787@gmail.com> wrote:
On Thu, Mar 7, 2013 at 12:02 PM, Avery louie <inactive.e@gmail.com> wrote:the patent say gas evolution at the electrode will cause increased
> Could you just cast your electrodes into your gel? Will anything bad
> happen? I guess it would be hard to remove the electrodes, since they are
> fairly delicate.
>
resistance and eventually breaking the circuit unless aluminum and
palladium electrodes are used at opposite ends to absorb the O2 and
H2 gas.
> --A
>
> On Thu, Mar 7, 2013 at 2:07 PM, Nathan McCorkle <nmz787@gmail.com> wrote:
>>
>> Seems like it's just a marketing tactic, the second instruction says:
>> "Remove combs, add 300ml deionized water, add little running buffer at
>> both ends, or without running buffer when runing bufferless genotyping
>> gel."
>>
>> That most likely means the gel is buffered too. I think more
>> appropriate marketing would be 'liquid-free', if anything.
>>
>> Here's a patent that's about to expire on this type of system
>> (probably the same as the Invitrogen eGel)
>> http://www.google.com/patents?hl=en&lr=&vid=USPAT5209831
>>
>>
>> I'm trying to figure out what kind of buffer they're using, that's the
>> key to this '6 minute run'... but it's probably Sodium Borate or
>> Lithium Borate (i.e. Faster Better Media LLC) here's 'their' patent:
>> http://www.6mgel.com/6mgel%20patent.pdf
>>
>> And the work Faster Better Media LLC based their products on:
>> http://en.wikipedia.org/wiki/SB_buffer
>>
>> http://www.biotechniques.com/multimedia/archive/00037/BTN_A_04374ST04_O_37093a.pdf
>>
>>
>> --
>> -Nathan
>>
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-Nathan
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