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Top : New Forum Archives (2009-): : Molecular-Cloning
631. Stable transfection - (reply: 2)
632. Using normal competent cells in electroporation method? - (reply: 1)
633. an effective way to do a yeast colony pcr - (reply: 2)
634. pGEM-T Easy vector contamination - (reply: 2)
635. recover old transformed DH5 - (reply: 1)
636. NZY+Broth can be replaced by LB Broth in mutagenesis exp - (reply: 2)
637. oligo(dt) 15 vs random primers - (reply: 3)
638. I need bynary vector pART27 - (reply: 1)
639. Plasmid with two similar bacterial ORIs - Can it be transformed into bacteria?? - (reply: 2)
640. Why don't I get the expected entry clones when I use the gateway system?? - (reply: 2)
641. Need help verifying promotor of a PUC19 based plasmid - (reply: 1)
642. cloning into Pgem t easy - (reply: 1)
643. How to get pure protein of a gene - (reply: 3)
644. How to insert genes into chromosome of E. coli - (reply: 1)
645. Gene synthesis - (reply: 2)
646. I canīt obtain the amount of DNA required for ligation of blunt ends - (reply: 2)
647. Pls help me with this plasmid!!! - (reply: 1)
648. Problems with Restriction Digest Results - (reply: 7)
649. Methods of plasmid transformation? only heat shock? - (reply: 1)
650. Digestion - (reply: 2)
651. Digestion of Genomic DNA - (reply: 1)
652. Isolation of a Gene of Interest for Subcloning - (reply: 8)
653. E.coli grow on neg. control - (reply: 1)
654. Transformed cells have many mutations! pET-46 Ek/LIC + sequence verified ins - (reply: 1)
655. Need help troubleshooting digest. - (reply: 1)
656. Competent cells question: JM101 vs DH5alpha - (reply: 2)
657. How to avoid plasmid instability - (reply: 4)
658. Question Help - (reply: 1)
659. Shear-induced damage of plasmid by vortexing - (reply: 1)
660. Problems with blunt end ligation - (reply: 3)