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Top : New Forum Archives (2009-): : Tissue-and-Cell-Culture
931. HaCaT info. & HaCaT TEM - (reply: 1)
932. lentivirus for invitro study - (reply: 1)
933. HT1080 karyotype - (reply: 1)
934. Can buffering strength of media reduce with time ? - (reply: 4)
935. MDA-MB-231 cells question - (reply: 3)
936. Help!my 293T stop growth and become slim 24h after 1:3 splitting - unless you change new medium for them 24h after splitting (reply: 3)
937. Stable transfection selection - (reply: 3)
938. Bone marrow shipping - (reply: 3)
939. Why does my media turn alkaline not acidic? - MCF-7 in EMEM (reply: 4)
940. lncap and MCF-7become ethanol sensitive? - are lncap cells and MCF-7 cells ethanol-sensitive? (reply: 2)
941. How much protein from a confluent 6 well plate? - (reply: 5)
942. problems with yeast contamination - (reply: 1)
943. Help me - Are my cells infected with something or could this be unsusual morphol - (reply: 5)
944. how to dissociate cells for cell migration assay - (reply: 3)
945. Isolation of cytotrophoblasts - (reply: 1)
946. Help with DNA Quantification - Cell lysis for DNA quantification using Hoechst 33258 (reply: 2)
947. basic question on passage ratios - (reply: 1)
948. I did not change the media the day after transfecting 293T cells. Are they going - (reply: 1)
949. Non Mouse / Human Cell Line that is easily transfected - (reply: 2)
950. Best practice use of antibiotics - (reply: 2)
951. suspension cell transient transfection - (reply: 10)
952. elemination yeast contamination - (reply: 1)
953. Harvesting Mouse Organs for Mouse Tissue Extracts - (reply: 2)
954. abnormal nuclear morphology after treating shRNA - confocal, shRNA, nuclear morphology, cell division (reply: 2)
955. recommendation wanted for microscope - (reply: 2)
956. counting cells - (reply: 3)
957. need advice about antibody characterization - (reply: 4)
958. cell confluency & effect on cells...?? - (reply: 4)
959. mycoplasma false positive - Luminescence false positives for myco (reply: 2)
960. (CELL CULTURE) Serious advice needed regarding my career..? - (reply: 2)