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991. DNA Storage - (reply: 10)
992. RBC LYSIS BUFFER - a good substitute of sucrose? - (reply: 5)
993. Luciferase assay - expected range of raw reading values - (reply: 1)
994. compare between 2 or more genes - (reply: 1)
995. sample preservation for RNA extraction - (reply: 1)
996. Designing primers for the ORFs - (reply: 9)
997. Bioinformatics Software - (reply: 2)
998. Low yields with quiagen midi kit - (reply: 2)
999. RNA extraction from blood stain - (reply: 1)
1000. Knocking out non-essential gene - (reply: 2)
1001. PCR with phophorylated primers - (reply: 1)
1002. Nanodrop absorbtion at 290 nm??? - (reply: 1)
1003. Plasmid sequencing without primers - (reply: 1)
1004. Either too low or too high a260/a230 - (reply: 5)
1005. RNA purity - (reply: 3)
1006. RNA Buffer Extraction - (reply: 3)
1007. wet chamber for ISH - (reply: 4)
1008. Convertion of 100% glycerol to 80% - (reply: 1)
1009. Difference between EST and cDNA? - (reply: 4)
1010. question related to mutagenesis - (reply: 1)
1011. Genotyping by allele specific PCR - (reply: 6)
1012. Size and composition of spacer between protein and tag? - (reply: 4)
1013. Wacky BioAnalyzer Results - (reply: 12)
1014. How much of plasmid should be cut to see the gene - (reply: 1)
1015. Plasmid sequencing - (reply: 1)
1016. NO Insert found in the Colony PCR - (reply: 15)
1017. Sequencing shows different results when sequenced from the other end - (reply: 3)
1018. Possible non-specific staining of ribo-probe in Fluorescence in situ hybridisati - (reply: 1)
1019. T7 Expression System - (reply: 5)
1020. Purification of oligos for EMSA - (reply: 1)
992. RBC LYSIS BUFFER - a good substitute of sucrose? - (reply: 5)
993. Luciferase assay - expected range of raw reading values - (reply: 1)
994. compare between 2 or more genes - (reply: 1)
995. sample preservation for RNA extraction - (reply: 1)
996. Designing primers for the ORFs - (reply: 9)
997. Bioinformatics Software - (reply: 2)
998. Low yields with quiagen midi kit - (reply: 2)
999. RNA extraction from blood stain - (reply: 1)
1000. Knocking out non-essential gene - (reply: 2)
1001. PCR with phophorylated primers - (reply: 1)
1002. Nanodrop absorbtion at 290 nm??? - (reply: 1)
1003. Plasmid sequencing without primers - (reply: 1)
1004. Either too low or too high a260/a230 - (reply: 5)
1005. RNA purity - (reply: 3)
1006. RNA Buffer Extraction - (reply: 3)
1007. wet chamber for ISH - (reply: 4)
1008. Convertion of 100% glycerol to 80% - (reply: 1)
1009. Difference between EST and cDNA? - (reply: 4)
1010. question related to mutagenesis - (reply: 1)
1011. Genotyping by allele specific PCR - (reply: 6)
1012. Size and composition of spacer between protein and tag? - (reply: 4)
1013. Wacky BioAnalyzer Results - (reply: 12)
1014. How much of plasmid should be cut to see the gene - (reply: 1)
1015. Plasmid sequencing - (reply: 1)
1016. NO Insert found in the Colony PCR - (reply: 15)
1017. Sequencing shows different results when sequenced from the other end - (reply: 3)
1018. Possible non-specific staining of ribo-probe in Fluorescence in situ hybridisati - (reply: 1)
1019. T7 Expression System - (reply: 5)
1020. Purification of oligos for EMSA - (reply: 1)