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Top : New Forum Archives (2009-): : General-Lab-Techniques
1021. converting OD 600 reading to DNA concentration - Totally having a brain hiccup (reply: 3)
1022. Filtering Copper Sulfate - (reply: 6)
1023. How can i get this solution soluble? - Lysis buffer (reply: 2)
1024. To thaw or not to thaw - (reply: 4)
1025. ACS LabGrade - Chemicals, reagents... (reply: 1)
1026. how to visualize a peptide - (reply: 11)
1027. Laser capture microdissection - capturing single cells (reply: 2)
1028. Forms of EDTA...? - (reply: 1)
1029. Agarose Gel Electrophoresis Problems - DNA bands appear to be weird on the gel (reply: 3)
1030. Working concentration - (reply: 9)
1031. how to prepare micromolar drug concentration - (reply: 4)
1032. Blow up my lab bench - again! - (reply: 3)
1033. Prepration of PBS-BSA-EDTA - The testing of PBS-BSA-EDTA (reply: 2)
1034. Destaining a coomassie sttained gel - (reply: 14)
1035. 5% agarose - (reply: 4)
1036. Help! % solution confusion - Making % stock solutions (reply: 4)
1037. R-Squared Values for a Standard Curve - (reply: 4)
1038. Too much failure in electrophoresis, am I doing the gel correctly? - (reply: 10)
1039. Disposal of coomassie stain - (reply: 3)
1040. Running multiple PCRs in a day - (reply: 7)
1041. plasmid extraction - why dilute (reply: 3)
1042. How to calculate the mitotic rate? - Should I calculate the area of a High Power Field (HPF)? (reply: 1)
1043. Sodium borate buffer gel problems - (reply: 5)
1044. Which pipette is the best? - (reply: 16)
1045. How to calibrate micropippete? - (reply: 5)
1046. pH adjustment - (reply: 1)
1047. Tips for visualizing very faint bands in agarose gels? - (The PCR ain't going to get better, so the gel must!) (reply: 15)
1048. phenol 5% help! - (reply: 3)
1049. How to store wet dialysis membranes once opened? - (reply: 4)
1050. Cellulose Membranes - Problem with my membrane (reply: 3)