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international online community for dna barcoding professionals

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Lab Operations

Come share protocols and troubleshooting experiences, compare techniques, and discuss collaborative efforts.

Members: 73
Latest Activity: on Thursday

Discussion Forum

Exo-sap it clean-up? 2 Replies

Hello everyone,I'm in the sequencing stage of my M.Sc. research project, and I'm not getting very clean results so far.  I'm working with bivalve species found on the US East Coast (oysters,…Continue

Started by Lyndell M. Bade. Last reply by Lyndell M. Bade May 31, 2012.

Sharing Lab Protocols 7 Replies

One of the biggest goals of the Community Network is to share information among barcoders, and information about lab protocols is a very high priority. If you have documents that describe the…Continue

Started by David E. Schindel. Last reply by Gerald Griffin Oct 14, 2011.

Outsourcing DNA extraction and sequencing 3 Replies

We are looking into possibilities for generating barcode data from 3500 Indonesian plant species and we are considering sending our samples out for DNA extracting and sequencing.Does anyone have…Continue

Started by Gillian Dean. Last reply by Gillian Dean Jul 17, 2011.

electrophoresis equipment 1 Reply

 i got an email from someone asking about the type of wire to use in a gel tank - it is platinum wire that should be used. for some reason i cant find the post that was in the email in lab…Continue

Started by Gillian Dean. Last reply by Patricia Escalante Dec 19, 2010.

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Comment by Wonhoon, Lee on December 27, 2010 at 12:31am

Hi. I’m Wonhoon and working as postdoctoral position at Seoul National University (South Korea). I’m interesting in Korean Forest Insect Pests DNA barcoding. Until now, I have made barcode sequences about 200 species belong to six orders. I hope to learn many developed methods and share my experiences related in barcode researches in this community.

Thank you very much.

 Wonhoon Lee

Comment by Thomas Horn on August 28, 2010 at 4:01pm
Hi, i am currently confronted with very weak matK amplification of some species. We use dried material to extract DNA from. I am still not convinced that the extraction is the problem.
Did your group solve their problems?
Comment by Diego Pignataro on March 2, 2010 at 4:11pm
Hi!
My group is having some problems with matK amplification for fresh and herbarium samples, anybody have a recommendation or a protocol to follow? to improve the PCR reaction?

thanks a lot


Diego
 

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