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Top : New Forum Archives (2009-): : Molecular-Cloning
601. should I do blunt end my pcr product before ligation - (reply: 2)
602. Maxiprep of freeze/thawed pellet. - (reply: 1)
603. Digest with AarI and Pml I - (reply: 1)
604. Help with CGL gene cloning problems - (reply: 1)
605. screening for GPF - (reply: 10)
606. Creating a pGEM-T easy + insert sequence map - (reply: 1)
607. where to get vector overexpressing caveolin-1? - (reply: 2)
608. Colony PCR works but DNA yeild very low after miniprep - (reply: 2)
609. pINDUCER series - (reply: 1)
610. LZRS vector details - (reply: 1)
611. 12.4kb vector 6.7kb insert - (reply: 2)
612. Stable transfection - (reply: 2)
613. Using normal competent cells in electroporation method? - (reply: 1)
614. an effective way to do a yeast colony pcr - (reply: 2)
615. pGEM-T Easy vector contamination - (reply: 2)
616. recover old transformed DH5 - (reply: 1)
617. NZY+Broth can be replaced by LB Broth in mutagenesis exp - (reply: 2)
618. oligo(dt) 15 vs random primers - (reply: 3)
619. I need bynary vector pART27 - (reply: 1)
620. Plasmid with two similar bacterial ORIs - Can it be transformed into bacteria?? - (reply: 2)
621. Why don't I get the expected entry clones when I use the gateway system?? - (reply: 2)
622. Need help verifying promotor of a PUC19 based plasmid - (reply: 1)
623. cloning into Pgem t easy - (reply: 1)
624. How to get pure protein of a gene - (reply: 3)
625. How to insert genes into chromosome of E. coli - (reply: 1)
626. Gene synthesis - (reply: 2)
627. I canīt obtain the amount of DNA required for ligation of blunt ends - (reply: 2)
628. Pls help me with this plasmid!!! - (reply: 1)
629. Problems with Restriction Digest Results - (reply: 7)
630. Methods of plasmid transformation? only heat shock? - (reply: 1)