Hello Sol,

You first should choose the fragments you want to amplify and adjust your DNA extraction method. The bigger your fragments, the more DNA and high quality you will need to use. I have extracted DNA using a standard Phenol-Chloroform protocol from mites which are also very small, and had approx. 50ng/uL DNA at the end, which was more than enough to amplify a 950bp CoxI fragment.

Hope it helps...

Cheers

Alex

Dear Sol

I think you will get enough DNA for barcoding out of a leg if you can pull it from your specimens.

The question is whether it makes sense for you to use NDE (non-destructive DNA-extraction). At least in ants you might be happy with what you get (the cleared cuticle, which you can wholemount then.

We always use NDE in Protura, which often are below 1mm of length. I would guess that we never had the Problem of too few tissue for DNA-barcoding up till now.

greetings

nikola

P.S. you can see our protocols, but there is plenty of literature on NDE for sure also with beetles and ants

https://www.researchgate.net/publication/260645744_Where_Taxonomy_Based_on_Subtle_Morphological_Differences_Is_Perfectly_Mirrored_by_Huge_Genetic_Distances_DNA_Barcoding_in_Protura_%28Hexapoda%29

https://www.researchgate.net/publication/258217025_Confocal_imaging_of_the_exo-_and_endoskeleton_of_Protura_after_non-destructive_DNA_extraction

Article Where Taxonomy Based on Subtle Morphological Differences Is ...

Article Confocal imaging of the exo- and endoskeleton of Protura aft...

Thanks so much for your responses, this is really helpful info and I reckon from this that two legs from even the very small specimens should be sufficient for the PCR.

Cheers,

Sol