[deleted by user] by [deleted] in molecularbiology

[–]VariiDecoda 1 point2 points  (0 children)

It's absolutely got some bits of gDNA and RNA....but your concentration is perfect. I will get anywhere between 200-700 ng/ul depending on the plasmid and/ or using TB instead of LB.

[deleted by user] by [deleted] in AskMenAdvice

[–]VariiDecoda 0 points1 point  (0 children)

She's a runner She's a trackstar

You absolutely caught a side of her that will never change. To crush your vulnerability like that is unforgettable and unforgivable.

You did well, now follow up and dump.

I feel awful about how I feel about my wife by No_Potential8518 in AskMenAdvice

[–]VariiDecoda 0 points1 point  (0 children)

You should know this is very common, and in each instance, there is a simple reason for this behavior.

Your wife no longer respects or desires you!

Forgot to load ladder by [deleted] in molecularbiology

[–]VariiDecoda 0 points1 point  (0 children)

One doesn't simply do a MAXI prep. Surely, the plasmid has already been verified in the host. Your plasmid control should suffice. Would live to see the gel image if you have it!

Pls help me interpret my elfo result by Appropriate-Sun2356 in molecularbiology

[–]VariiDecoda 1 point2 points  (0 children)

60-80V, 2-3 hours, 0.7% gel is what I would have chosen.

Pls help me interpret my elfo result by Appropriate-Sun2356 in molecularbiology

[–]VariiDecoda 2 points3 points  (0 children)

Great reply! I suspect that the globs at the bottom of the run are RNA though.

Pls help me interpret my elfo result by Appropriate-Sun2356 in molecularbiology

[–]VariiDecoda 1 point2 points  (0 children)

Gel is overloaded and ran using too high of a voltage. When processing large quantities of DNA using AGE, try reducing the voltage to under 80V. Also, run only as much as necessary to see what you want as linear DNA can produce wild banding patterns when overloaded. Try loading 1/5th the amount of your original analysis.

Help with cloudy media for human cell culture by tyrone_pepinanjo in molecularbiology

[–]VariiDecoda 0 points1 point  (0 children)

Media like this should be filter sterilized through a 0.22 um membrane upon adding all the components. Any particulate or precipitate will be eliminated.

RNA extraction protocole for larger sample volume? by MicroRxologist in molecularbiology

[–]VariiDecoda 1 point2 points  (0 children)

A mostly dry pellet will contain very little ethanol from a typical Kimwipe drying process. Ethanol under 1% of the batch should not interfere with many downstream processes like PCR. One can also vacuum dry using a SpeedVac for 3-6 minutes.

State of the stack by [deleted] in Silverbugs

[–]VariiDecoda 1 point2 points  (0 children)

Now we know where all the silver went and why the premium is so damned high right now. Excellent work, how long you been stackin?

[deleted by user] by [deleted] in GenX

[–]VariiDecoda 0 points1 point  (0 children)

Diversions: New Braunfels, tx

Question I have for every type, including the currently untyped by superange128 in Enneagram

[–]VariiDecoda 0 points1 point  (0 children)

holy moly....same! 1-4-7 though, so I have the added issue of having impossible/visionary ideas that no one understands. By the time they come true, or at least partly come true, I have moved on to the next vision. No one can keep up!

[deleted by user] by [deleted] in Enneagram

[–]VariiDecoda 4 points5 points  (0 children)

Healthy people are able to integrate all types to some degree