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Top : New Forum Archives (2009-): : Molecular-Biology
2071. How Much BrET? - In TAE (reply: 2)
2072. pfu vs long pcr mix - (reply: 7)
2073. Time required for digestion using Fast digest enzymes - (reply: 7)
2074. HELP! - How to read genetics (reply: 1)
2075. IFU, MOI, lentiviral vectors - (reply: 1)
2076. Genomic DNA Library - Problem of reactivity - Genomic DNA library screening with antibody (reply: 1)
2077. Sequencing - (reply: 1)
2078. Can be alkaline phosphatise inhibit by PBS? - (reply: 2)
2079. RCAS virus infection - (reply: 3)
2080. DENATURING AGAROSE GEL FOR RNA - (reply: 1)
2081. circular RNA - (reply: 3)
2082. Invitrogen REs and NEB Buffers - Are they compatible? (reply: 1)
2083. Incompatible restriction sites - Will E.coli ligate for me? (reply: 2)
2084. Where can you get the sequence of one exon of a gene? - (reply: 3)
2085. microrna quantitation ---use northern blot or qrt-pcr? - (reply: 1)
2086. proteinase K problem - DNA loss during proteinase K treatment (reply: 1)
2087. ethanol precipitation - (reply: 1)
2088. RCAS virus stability - (reply: 2)
2089. concentration for cloning - (reply: 1)
2090. precise definition of exon? - (reply: 3)
2091. WGA kits - experiences? (reply: 3)
2092. why the bands migrate lower in the gel EMSA? - as I increase protein concentration (reply: 1)
2093. How do you detect large genomic deletion - (reply: 1)
2094. Dilution problem - 10 ug/ml to.... (reply: 1)
2095. Southern blot for deletion detection....HELP!!!!! - (reply: 3)
2096. salt condition of EMSA - I need to adjust salt condition to improve the specificity of my EMSA (reply: 1)
2097. Hybriization basic (?) question - (reply: 3)
2098. Gateway and Entry Vectors. - (reply: 1)
2099. dna storage buffer - (reply: 3)
2100. innoculated LB amp plate at 4C - (reply: 2)