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2101. some Q's about dna microarray - (reply: 2)
2102. cDNA concentration higher than original RNA - (reply: 4)
2103. How Much BrET? - In TAE (reply: 2)
2104. pfu vs long pcr mix - (reply: 7)
2105. Time required for digestion using Fast digest enzymes - (reply: 7)
2106. HELP! - How to read genetics (reply: 1)
2107. IFU, MOI, lentiviral vectors - (reply: 1)
2108. Genomic DNA Library - Problem of reactivity - Genomic DNA library screening with antibody (reply: 1)
2109. Sequencing - (reply: 1)
2110. Can be alkaline phosphatise inhibit by PBS? - (reply: 2)
2111. RCAS virus infection - (reply: 3)
2112. DENATURING AGAROSE GEL FOR RNA - (reply: 1)
2113. circular RNA - (reply: 3)
2114. Invitrogen REs and NEB Buffers - Are they compatible? (reply: 1)
2115. Incompatible restriction sites - Will E.coli ligate for me? (reply: 2)
2116. Where can you get the sequence of one exon of a gene? - (reply: 3)
2117. microrna quantitation ---use northern blot or qrt-pcr？ - (reply: 1)
2118. proteinase K problem - DNA loss during proteinase K treatment (reply: 1)
2119. ethanol precipitation - (reply: 1)
2120. RCAS virus stability - (reply: 2)
2121. concentration for cloning - (reply: 1)
2122. precise definition of exon? - (reply: 3)
2123. WGA kits - experiences? (reply: 3)
2124. why the bands migrate lower in the gel EMSA? - as I increase protein concentration (reply: 1)
2125. How do you detect large genomic deletion - (reply: 1)
2126. Dilution problem - 10 ug/ml to.... (reply: 1)
2127. Southern blot for deletion detection....HELP!!!!! - (reply: 3)
2128. salt condition of EMSA - I need to adjust salt condition to improve the specificity of my EMSA (reply: 1)
2129. Hybriization basic (?) question - (reply: 3)
2130. Gateway and Entry Vectors. - (reply: 1)
2102. cDNA concentration higher than original RNA - (reply: 4)
2103. How Much BrET? - In TAE (reply: 2)
2104. pfu vs long pcr mix - (reply: 7)
2105. Time required for digestion using Fast digest enzymes - (reply: 7)
2106. HELP! - How to read genetics (reply: 1)
2107. IFU, MOI, lentiviral vectors - (reply: 1)
2108. Genomic DNA Library - Problem of reactivity - Genomic DNA library screening with antibody (reply: 1)
2109. Sequencing - (reply: 1)
2110. Can be alkaline phosphatise inhibit by PBS? - (reply: 2)
2111. RCAS virus infection - (reply: 3)
2112. DENATURING AGAROSE GEL FOR RNA - (reply: 1)
2113. circular RNA - (reply: 3)
2114. Invitrogen REs and NEB Buffers - Are they compatible? (reply: 1)
2115. Incompatible restriction sites - Will E.coli ligate for me? (reply: 2)
2116. Where can you get the sequence of one exon of a gene? - (reply: 3)
2117. microrna quantitation ---use northern blot or qrt-pcr？ - (reply: 1)
2118. proteinase K problem - DNA loss during proteinase K treatment (reply: 1)
2119. ethanol precipitation - (reply: 1)
2120. RCAS virus stability - (reply: 2)
2121. concentration for cloning - (reply: 1)
2122. precise definition of exon? - (reply: 3)
2123. WGA kits - experiences? (reply: 3)
2124. why the bands migrate lower in the gel EMSA? - as I increase protein concentration (reply: 1)
2125. How do you detect large genomic deletion - (reply: 1)
2126. Dilution problem - 10 ug/ml to.... (reply: 1)
2127. Southern blot for deletion detection....HELP!!!!! - (reply: 3)
2128. salt condition of EMSA - I need to adjust salt condition to improve the specificity of my EMSA (reply: 1)
2129. Hybriization basic (?) question - (reply: 3)
2130. Gateway and Entry Vectors. - (reply: 1)