|
931. HUGE colonies everywhere! - (reply: 4)
932. subcloning dengue NS1 gene problems - molecular biology, cloning (reply: 5)
933. can I just ethanol precipitate Klenow? - without deactivating it? (reply: 4)
934. getting rid of undigested vector - (reply: 5)
935. Fusion protein questions - Botched deletion primer (reply: 2)
936. AscI digestion of plasmid - Problem with AscI digestion of plasmid DNA (reply: 6)
937. Qiagen DNA Kits - Extra bands (reply: 7)
938. Cloning Problem - (reply: 2)
939. TA cloning help - (reply: 4)
940. my experience with cloning - (reply: 2)
941. problem with designer - (reply: 1)
942. question for the PCR to cloning construct - (reply: 9)
943. design primer - (reply: 5)
944. Problems using gentamicin plasmids - (reply: 6)
945. Agaroase gel analysis of ligation reaction - (reply: 6)
946. so how do blunt ends stick together? - (reply: 4)
947. how can I shift the frame? - please help!!!! (reply: 14)
948. Problem on restriction digest - Inquire (reply: 11)
949. Insert is double the size than vector - (reply: 6)
950. transformation - random genomic inserts (reply: 3)
951. cDNA problem - (reply: 5)
952. oligo annealing - (reply: 3)
953. Multiple transformation - How many plasmids is it possible to transform at the same time ? (reply: 2)
954. Help with ligation using Topo TA - (reply: 7)
955. Restriction digest - volume of restriction digest (reply: 2)
956. Gene cloning - Gene library (reply: 1)
957. competen cell - (reply: 3)
958. Problem on negative control in Xgal - Question, suggestion (reply: 1)
959. impossible single enzyme cut - (reply: 1)
960. why the insert is always in opposite orientation - (reply: 1)
932. subcloning dengue NS1 gene problems - molecular biology, cloning (reply: 5)
933. can I just ethanol precipitate Klenow? - without deactivating it? (reply: 4)
934. getting rid of undigested vector - (reply: 5)
935. Fusion protein questions - Botched deletion primer (reply: 2)
936. AscI digestion of plasmid - Problem with AscI digestion of plasmid DNA (reply: 6)
937. Qiagen DNA Kits - Extra bands (reply: 7)
938. Cloning Problem - (reply: 2)
939. TA cloning help - (reply: 4)
940. my experience with cloning - (reply: 2)
941. problem with designer - (reply: 1)
942. question for the PCR to cloning construct - (reply: 9)
943. design primer - (reply: 5)
944. Problems using gentamicin plasmids - (reply: 6)
945. Agaroase gel analysis of ligation reaction - (reply: 6)
946. so how do blunt ends stick together? - (reply: 4)
947. how can I shift the frame? - please help!!!! (reply: 14)
948. Problem on restriction digest - Inquire (reply: 11)
949. Insert is double the size than vector - (reply: 6)
950. transformation - random genomic inserts (reply: 3)
951. cDNA problem - (reply: 5)
952. oligo annealing - (reply: 3)
953. Multiple transformation - How many plasmids is it possible to transform at the same time ? (reply: 2)
954. Help with ligation using Topo TA - (reply: 7)
955. Restriction digest - volume of restriction digest (reply: 2)
956. Gene cloning - Gene library (reply: 1)
957. competen cell - (reply: 3)
958. Problem on negative control in Xgal - Question, suggestion (reply: 1)
959. impossible single enzyme cut - (reply: 1)
960. why the insert is always in opposite orientation - (reply: 1)