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Top : New Forum Archives (2009-): : Molecular-Biology
1681. No band after digestion - (reply: 4)
1682. Problem with ligation - Insert into the "wrong" vector (reply: 11)
1683. finding promoter - (reply: 1)
1684. Problem in expression of protein cloned in pcDNA3 - (reply: 1)
1685. Cloning in pCR2.1 plasmid - (reply: 7)
1686. How long can DNA precipitate at -20? - (reply: 6)
1687. Nucleotides with different font size - (reply: 2)
1688. primer sequence problem - (reply: 2)
1689. Maxiprep using alkaline lysis, very high OD, but low intensity on gel - (reply: 2)
1690. lambda phage library - (reply: 1)
1691. More colonies fron vector only control? - (reply: 1)
1692. Mutagenesis again - (reply: 1)
1693. standard curve method for Q-PCR - (reply: 3)
1694. PCR - No Band formation - (reply: 3)
1695. GEL SMEAR - (reply: 4)
1696. Cloning a 3.5Kb fragment for sequencing - P-gem T-easy. (reply: 2)
1697. Localization of kanamycin resistance protein - (reply: 1)
1698. dna sequencing - (reply: 1)
1699. Biotinylated oligo separation - (reply: 4)
1700. Advice on Cloning Strategy - (reply: 4)
1701. Miniprep DNA-strange nanodrop peak at 240-250nm? - (reply: 4)
1702. Ligation Problem? Or Something else...? - (reply: 3)
1703. Ligation of Blunt PCR Product - (reply: 1)
1704. Help Help, sequencing not working - Sequencing-noisy (reply: 4)
1705. Why do I always get these same 4 point mutations ? Help !!! - (reply: 2)
1706. Adapters - (reply: 2)
1707. RNA extraction: no pellet... - (reply: 2)
1708. Slight Smear after Digestion - (reply: 2)
1709. RNeasy: B-Me vs. DTT - (reply: 1)
1710. ChIP purification method - (reply: 7)