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Top : New Forum Archives (2009-): : Molecular-Cloning
631. Creating a pGEM-T easy + insert sequence map - (reply: 1)
632. where to get vector overexpressing caveolin-1? - (reply: 2)
633. Colony PCR works but DNA yeild very low after miniprep - (reply: 2)
634. pINDUCER series - (reply: 1)
635. LZRS vector details - (reply: 1)
636. 12.4kb vector 6.7kb insert - (reply: 2)
637. Stable transfection - (reply: 2)
638. Using normal competent cells in electroporation method? - (reply: 1)
639. an effective way to do a yeast colony pcr - (reply: 2)
640. pGEM-T Easy vector contamination - (reply: 2)
641. recover old transformed DH5 - (reply: 1)
642. NZY+Broth can be replaced by LB Broth in mutagenesis exp - (reply: 2)
643. oligo(dt) 15 vs random primers - (reply: 3)
644. I need bynary vector pART27 - (reply: 1)
645. Plasmid with two similar bacterial ORIs - Can it be transformed into bacteria?? - (reply: 2)
646. Why don't I get the expected entry clones when I use the gateway system?? - (reply: 2)
647. Need help verifying promotor of a PUC19 based plasmid - (reply: 1)
648. cloning into Pgem t easy - (reply: 1)
649. How to get pure protein of a gene - (reply: 3)
650. How to insert genes into chromosome of E. coli - (reply: 1)
651. Gene synthesis - (reply: 2)
652. I canīt obtain the amount of DNA required for ligation of blunt ends - (reply: 2)
653. Pls help me with this plasmid!!! - (reply: 1)
654. Problems with Restriction Digest Results - (reply: 7)
655. Methods of plasmid transformation? only heat shock? - (reply: 1)
656. Digestion - (reply: 2)
657. Digestion of Genomic DNA - (reply: 1)
658. Isolation of a Gene of Interest for Subcloning - (reply: 8)
659. E.coli grow on neg. control - (reply: 1)
660. Transformed cells have many mutations! pET-46 Ek/LIC + sequence verified ins - (reply: 1)