Discussion of all aspects of biological molecules, biochemical processes and laboratory procedures in the field.
1 post • Page 1 of 1
I am working on constructing a phage library to express antibodies and currently I am doing the Fab library constructing work. I did PCR and got light chain (LC) products. There is a LC stuffer in the vector so I digested and gel purified the digested phagemid vector and the LC stuffer as a control. I tried to ligate the digested LC or LC stuffer with the vector. To test, I transformed the ligation product into DH5-alpha competent cells using regular heat shock transformation method. After picking colonies and digesting the miniprep products, I run a gel to check and the results are shown in the picture attached. From left to right, lanes 1-5 are the 5 colonies of vector-LC ligation while lanes 6-10 are the vector-LC stuffer colonies. Lane 13 is the purified vector as control. Apparently, there is some problem with the LC purification so the ligation-transformation did not work, I think? I did gel purify the LC product so I don’t know what to do right now. Any suggestion would be greatly appreciated!
Who is online
Users browsing this forum: No registered users and 8 guests