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Top : New Forum Archives (2009-): : Molecular-Biology
1651. RNA extraction from stained cells - (reply: 2)
1652. agarose gel electrophoresis - fluorescence which will not migrate from well and does not disappear a (reply: 5)
1653. No band after digestion - (reply: 4)
1654. Problem with ligation - Insert into the "wrong" vector (reply: 11)
1655. finding promoter - (reply: 1)
1656. Problem in expression of protein cloned in pcDNA3 - (reply: 1)
1657. Cloning in pCR2.1 plasmid - (reply: 7)
1658. How long can DNA precipitate at -20? - (reply: 6)
1659. Nucleotides with different font size - (reply: 2)
1660. primer sequence problem - (reply: 2)
1661. Maxiprep using alkaline lysis, very high OD, but low intensity on gel - (reply: 2)
1662. lambda phage library - (reply: 1)
1663. More colonies fron vector only control? - (reply: 1)
1664. Mutagenesis again - (reply: 1)
1665. standard curve method for Q-PCR - (reply: 3)
1666. PCR - No Band formation - (reply: 3)
1667. GEL SMEAR - (reply: 4)
1668. Cloning a 3.5Kb fragment for sequencing - P-gem T-easy. (reply: 2)
1669. Localization of kanamycin resistance protein - (reply: 1)
1670. dna sequencing - (reply: 1)
1671. Biotinylated oligo separation - (reply: 4)
1672. Advice on Cloning Strategy - (reply: 4)
1673. Miniprep DNA-strange nanodrop peak at 240-250nm? - (reply: 4)
1674. Ligation Problem? Or Something else...? - (reply: 3)
1675. Ligation of Blunt PCR Product - (reply: 1)
1676. Help Help, sequencing not working - Sequencing-noisy (reply: 4)
1677. Why do I always get these same 4 point mutations ? Help !!! - (reply: 2)
1678. Adapters - (reply: 2)
1679. RNA extraction: no pellet... - (reply: 2)
1680. Slight Smear after Digestion - (reply: 2)