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Top : New Forum Archives (2009-): : Molecular-Biology
1561. Selecting Lethal Mutants? - (reply: 1)
1562. RNA extraction from stained cells - (reply: 2)
1563. agarose gel electrophoresis - fluorescence which will not migrate from well and does not disappear a (reply: 5)
1564. No band after digestion - (reply: 4)
1565. Problem with ligation - Insert into the "wrong" vector (reply: 11)
1566. finding promoter - (reply: 1)
1567. Problem in expression of protein cloned in pcDNA3 - (reply: 1)
1568. Cloning in pCR2.1 plasmid - (reply: 7)
1569. How long can DNA precipitate at -20? - (reply: 6)
1570. Nucleotides with different font size - (reply: 2)
1571. primer sequence problem - (reply: 2)
1572. Maxiprep using alkaline lysis, very high OD, but low intensity on gel - (reply: 2)
1573. lambda phage library - (reply: 1)
1574. More colonies fron vector only control? - (reply: 1)
1575. Mutagenesis again - (reply: 1)
1576. standard curve method for Q-PCR - (reply: 3)
1577. PCR - No Band formation - (reply: 3)
1578. GEL SMEAR - (reply: 4)
1579. Cloning a 3.5Kb fragment for sequencing - P-gem T-easy. (reply: 2)
1580. Localization of kanamycin resistance protein - (reply: 1)
1581. dna sequencing - (reply: 1)
1582. Biotinylated oligo separation - (reply: 4)
1583. Advice on Cloning Strategy - (reply: 4)
1584. Miniprep DNA-strange nanodrop peak at 240-250nm? - (reply: 4)
1585. Ligation Problem? Or Something else...? - (reply: 3)
1586. Ligation of Blunt PCR Product - (reply: 1)
1587. Help Help, sequencing not working - Sequencing-noisy (reply: 4)
1588. Why do I always get these same 4 point mutations ? Help !!! - (reply: 2)
1589. Adapters - (reply: 2)
1590. RNA extraction: no pellet... - (reply: 2)