|
1561. some Q's about dna microarray - (reply: 2)
1562. cDNA concentration higher than original RNA - (reply: 4)
1563. How Much BrET? - In TAE (reply: 2)
1564. pfu vs long pcr mix - (reply: 7)
1565. Time required for digestion using Fast digest enzymes - (reply: 7)
1566. HELP! - How to read genetics (reply: 1)
1567. IFU, MOI, lentiviral vectors - (reply: 1)
1568. Genomic DNA Library - Problem of reactivity - Genomic DNA library screening with antibody (reply: 1)
1569. Sequencing - (reply: 1)
1570. Can be alkaline phosphatise inhibit by PBS? - (reply: 2)
1571. RCAS virus infection - (reply: 3)
1572. DENATURING AGAROSE GEL FOR RNA - (reply: 1)
1573. circular RNA - (reply: 3)
1574. Invitrogen REs and NEB Buffers - Are they compatible? (reply: 1)
1575. Incompatible restriction sites - Will E.coli ligate for me? (reply: 2)
1576. Where can you get the sequence of one exon of a gene? - (reply: 3)
1577. microrna quantitation ---use northern blot or qrt-pcr？ - (reply: 1)
1578. proteinase K problem - DNA loss during proteinase K treatment (reply: 1)
1579. ethanol precipitation - (reply: 1)
1580. RCAS virus stability - (reply: 2)
1581. concentration for cloning - (reply: 1)
1582. precise definition of exon? - (reply: 3)
1583. WGA kits - experiences? (reply: 3)
1584. why the bands migrate lower in the gel EMSA? - as I increase protein concentration (reply: 1)
1585. How do you detect large genomic deletion - (reply: 1)
1586. Dilution problem - 10 ug/ml to.... (reply: 1)
1587. Southern blot for deletion detection....HELP!!!!! - (reply: 3)
1588. salt condition of EMSA - I need to adjust salt condition to improve the specificity of my EMSA (reply: 1)
1589. Hybriization basic (?) question - (reply: 3)
1590. Gateway and Entry Vectors. - (reply: 1)
1562. cDNA concentration higher than original RNA - (reply: 4)
1563. How Much BrET? - In TAE (reply: 2)
1564. pfu vs long pcr mix - (reply: 7)
1565. Time required for digestion using Fast digest enzymes - (reply: 7)
1566. HELP! - How to read genetics (reply: 1)
1567. IFU, MOI, lentiviral vectors - (reply: 1)
1568. Genomic DNA Library - Problem of reactivity - Genomic DNA library screening with antibody (reply: 1)
1569. Sequencing - (reply: 1)
1570. Can be alkaline phosphatise inhibit by PBS? - (reply: 2)
1571. RCAS virus infection - (reply: 3)
1572. DENATURING AGAROSE GEL FOR RNA - (reply: 1)
1573. circular RNA - (reply: 3)
1574. Invitrogen REs and NEB Buffers - Are they compatible? (reply: 1)
1575. Incompatible restriction sites - Will E.coli ligate for me? (reply: 2)
1576. Where can you get the sequence of one exon of a gene? - (reply: 3)
1577. microrna quantitation ---use northern blot or qrt-pcr？ - (reply: 1)
1578. proteinase K problem - DNA loss during proteinase K treatment (reply: 1)
1579. ethanol precipitation - (reply: 1)
1580. RCAS virus stability - (reply: 2)
1581. concentration for cloning - (reply: 1)
1582. precise definition of exon? - (reply: 3)
1583. WGA kits - experiences? (reply: 3)
1584. why the bands migrate lower in the gel EMSA? - as I increase protein concentration (reply: 1)
1585. How do you detect large genomic deletion - (reply: 1)
1586. Dilution problem - 10 ug/ml to.... (reply: 1)
1587. Southern blot for deletion detection....HELP!!!!! - (reply: 3)
1588. salt condition of EMSA - I need to adjust salt condition to improve the specificity of my EMSA (reply: 1)
1589. Hybriization basic (?) question - (reply: 3)
1590. Gateway and Entry Vectors. - (reply: 1)