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New Forum Archives (2009-)
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General-Lab-Techniques
691.
Software for labeling gel picture -
(reply: 1)
692.
converting OD 600 reading to DNA concentration - Totally having a brain hiccup
(reply: 3)
693.
Filtering Copper Sulfate -
(reply: 6)
694.
How can i get this solution soluble? - Lysis buffer
(reply: 2)
695.
To thaw or not to thaw -
(reply: 4)
696.
ACS LabGrade - Chemicals, reagents...
(reply: 1)
697.
how to visualize a peptide -
(reply: 11)
698.
Laser capture microdissection - capturing single cells
(reply: 2)
699.
Forms of EDTA...? -
(reply: 1)
700.
Agarose Gel Electrophoresis Problems - DNA bands appear to be weird on the gel
(reply: 3)
701.
Working concentration -
(reply: 9)
702.
how to prepare micromolar drug concentration -
(reply: 4)
703.
Blow up my lab bench - again! -
(reply: 3)
704.
Prepration of PBS-BSA-EDTA - The testing of PBS-BSA-EDTA
(reply: 2)
705.
Destaining a coomassie sttained gel -
(reply: 14)
706.
5% agarose -
(reply: 4)
707.
Help! % solution confusion - Making % stock solutions
(reply: 4)
708.
R-Squared Values for a Standard Curve -
(reply: 4)
709.
Too much failure in electrophoresis, am I doing the gel correctly? -
(reply: 10)
710.
Disposal of coomassie stain -
(reply: 3)
711.
Running multiple PCRs in a day -
(reply: 7)
712.
plasmid extraction - why dilute
(reply: 3)
713.
How to calculate the mitotic rate? - Should I calculate the area of a High Power Field (HPF)?
(reply: 1)
714.
Sodium borate buffer gel problems -
(reply: 5)
715.
Which pipette is the best? -
(reply: 16)
716.
How to calibrate micropippete? -
(reply: 5)
717.
pH adjustment -
(reply: 1)
718.
Tips for visualizing very faint bands in agarose gels? - (The PCR ain't going to get better, so the gel must!)
(reply: 15)
719.
phenol 5% help! -
(reply: 3)
720.
How to store wet dialysis membranes once opened? -
(reply: 4)
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