|
931. Problems with double transfections -cells die - (reply: 7)
932. competent cells - (reply: 2)
933. Isopropanol precipitatation overnight - (reply: 4)
934. RNAse treatment of genomic DNA - concentration and duration? - (reply: 1)
935. Unable to PCR!!!! - (reply: 3)
936. turbid DNA from maxiprep - (reply: 3)
937. no bacterial growth after inoculation - (reply: 4)
938. Low A260/A280 ratio after gel purification using Promega PCR Clean-up System - (reply: 2)
939. Anoyone knows a good reliable gel documentation system? - (reply: 4)
940. Isolating Genomic DNA from a small colony of cultured human cells - (reply: 1)
941. how to seperate double-digestion products on agarose gel - (reply: 14)
942. Insert lose in Phage display library - (reply: 6)
943. Help: I am loosing the DNA during PCR purification - (reply: 7)
944. PCR primer with no extra DNA end - (reply: 5)
945. Relative promoter strength - (reply: 2)
946. Dot Blot - Protein not adhering to membrane - (reply: 1)
947. Protein contamination - How to remove all protein from my DNA? - (reply: 3)
948. fluorescent -transfection problem - (reply: 1)
949. extract plasmids from transfected eukaryotic cells - (reply: 6)
950. I can't see anything in my gel. I need help - (reply: 1)
951. Restriction digestion of clones give undesired product - (reply: 3)
952. cDNA shelf-life - (reply: 1)
953. Phenol peak at RNA isolation with Trizol method - (reply: 1)
954. HELP!!!!absorbance peak and radioactivity do not match??? - (reply: 4)
955. cell culture confusion - (reply: 1)
956. COL E1 mutations in vector after sequencing - (reply: 1)
957. Strange band in colony PCR - (reply: 2)
958. stability of Phusion and Pfu at room temperature - (reply: 2)
959. what does HLA-G stand for? - (reply: 4)
960. saturation mutagenesis library problem again - (reply: 2)
932. competent cells - (reply: 2)
933. Isopropanol precipitatation overnight - (reply: 4)
934. RNAse treatment of genomic DNA - concentration and duration? - (reply: 1)
935. Unable to PCR!!!! - (reply: 3)
936. turbid DNA from maxiprep - (reply: 3)
937. no bacterial growth after inoculation - (reply: 4)
938. Low A260/A280 ratio after gel purification using Promega PCR Clean-up System - (reply: 2)
939. Anoyone knows a good reliable gel documentation system? - (reply: 4)
940. Isolating Genomic DNA from a small colony of cultured human cells - (reply: 1)
941. how to seperate double-digestion products on agarose gel - (reply: 14)
942. Insert lose in Phage display library - (reply: 6)
943. Help: I am loosing the DNA during PCR purification - (reply: 7)
944. PCR primer with no extra DNA end - (reply: 5)
945. Relative promoter strength - (reply: 2)
946. Dot Blot - Protein not adhering to membrane - (reply: 1)
947. Protein contamination - How to remove all protein from my DNA? - (reply: 3)
948. fluorescent -transfection problem - (reply: 1)
949. extract plasmids from transfected eukaryotic cells - (reply: 6)
950. I can't see anything in my gel. I need help - (reply: 1)
951. Restriction digestion of clones give undesired product - (reply: 3)
952. cDNA shelf-life - (reply: 1)
953. Phenol peak at RNA isolation with Trizol method - (reply: 1)
954. HELP!!!!absorbance peak and radioactivity do not match??? - (reply: 4)
955. cell culture confusion - (reply: 1)
956. COL E1 mutations in vector after sequencing - (reply: 1)
957. Strange band in colony PCR - (reply: 2)
958. stability of Phusion and Pfu at room temperature - (reply: 2)
959. what does HLA-G stand for? - (reply: 4)
960. saturation mutagenesis library problem again - (reply: 2)