Protocol Online logo
Top : New Forum Archives (2009-): : General-Lab-Techniques
931. What's the highest DNA concentration for PCR? - before being inhibited? (reply: 7)
932. intensity of flueroscence - (reply: 1)
933. Truncating or Rounding Sig Figs - all your ships are belong to us! (reply: 3)
934. Useful units of concentration - Which ones should I learn? (reply: 2)
935. Confused about mM and mmols and ml and L - HELP MEH! (reply: 2)
936. How to convert ng/ul to ug/ul - (reply: 3)
937. Procedures/Duties that starting lab assistants would do - HELP! (reply: 2)
938. u/ml and ug/ml - unit conversion (reply: 3)
939. HPLC calibration problem - (reply: 7)
940. Need help with dilution calculation - (reply: 2)
941. My RIPA cell lysis buffer - Western blot (reply: 3)
942. How long is DTT stable for at 4deg? - (reply: 5)
943. help me dilute this - (reply: 6)
944. Concerned about sterile technique - (reply: 1)
945. Agarose gel bands smear/ drag problem - (reply: 4)
946. Preparing BSA standards - (reply: 2)
947. How does the RBC lysis buffer work? - (reply: 9)
948. Molarity of citrate phosphate buffer - (reply: 1)
949. How to use the loading control? - (reply: 3)
950. Best way to apply pvp (or a viscous solution) to coverslip - Microscopy Technique (reply: 1)
951. How to make a buffer similar to PBS, pH 8,6? - (reply: 1)
952. Fluorometer vs luminometer - (reply: 1)
953. PAS negative - amylase or diastase digestion (reply: 1)
954. gel does not polymerize - (reply: 12)
955. Gel Storage for PAGE - Advance casting of polyacrylamide gels (reply: 2)
956. Culturing XL1 blue - MRF - (reply: 1)
957. How many volts/milliamps to run gel at? - (reply: 2)
958. How to get rid of phage contamination - (reply: 1)
959. EDTA to remove scales in Coffee Machine - Use of EDTA to remove scales from Coffee Machine (reply: 9)
960. liquid scintillation - (reply: 1)