100 jars.

You could clone a mushroom with a piece of tissue,use spores or a colonized grain. A flowhood isn't required and a glovebox would do fine. The problem with LC's is that you don't know if it is contaminated until you noc up a test jar. With agar you would know within a day or so if there is any contamination. If you don't mind testing each batch of LC you make then you could just stick with that. Another thing with Agar is you can isolate promising growth characteristics.

Here is a good video on Agar.
http://www.mediafire.com/download/w3m59na8dc93dee/Let's_Grow_Mushrooms!_2.6_-_Lets_Learn_Agar.mp4
 
Here is a good image on how you should "Swipe" your needle when applying spores.

2mxlh0i.jpg
 
Here is a good image on how you should "Swipe" your needle when applying spores.
2mxlh0i.jpg
That pattern is more for identification of various and different spores or bacteria. All the guy needs to do is squirt a drop or two in a plate and roll the plate around so the liquid spreads a bit. the spores will settle out after a day or so, and the liquid will evaporate soon enough, he may find that the spores have already germinated when the liquid is dry and he will see tiny spots of white all over the plate. If they look liquid, or quickly turn any color at all - then the syringe is contaminated - or the method is faulty, usually you can tell pretty quickly.
 
I inoced 500 ml LC ... and it sucked in my whole syringe. I then plastic wrapped it. Im not sure if this is right
 
So you put your whole spore solution in the 500 ml of LC?

While that is a shitload of spores to use I think you'll be okay.
 
Wait until they are 100 percent +5-7 more days for a consolidation period.


I thought you were doing grains?
 
I am. Inoced grains 6 days ago. Lc 3 days ago. Its the jars i started 3-4 weeks ago. The pics are on my profile. The ones i thought might have a prob. Just thiught mixing would help speed.
 
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