We narrowed to 28 results for: SEC
-
TypeProtocol...add 10 µL of the pool to 990 µL LB then perform a second and then third 1:100 dilution). Plate 100 µL of...not present on the most dilute plate, count the second plate (ie. the 1:10,000 dilution). After 12-18 ...
-
Protocol - pLKO.1 – TRC Cloning Vector
TypeProtocol...digestion with EcoRI and AgeI. The oligos from section B contain the shRNA sequence flanked by sequences...polymerase has difficulty reading through the secondary structure of the hairpin sequence. Back to Top... -
DNA Quantification
TypeProtocol...despite the accuracy of the NanoDrop, if two consecutive samples have significantly different concentrations... -
Protocol - How to Design Primers
TypeProtocol... be relatively simple and contain no internal secondary structure to avoid internal folding. One also ... -
Lab Safety for Biosafety Levels One and Two
TypeProtocol...impenetrable by a needle, and must be able to close securely. Biohazard signs should be placed in all areas... -
Using a Light Microscope Protocol
TypeProtocol...the microscope stage. If using a slide, you can secure it into place using the metal clips on the stage... -
AAV Purification by Iodixanol Gradient Ultracentrifugation
TypeProtocol.... Figure 3: Example of an SDS-PAGE gel of 10 consecutive gradient fractions followed by silver stain. ... -
Isolating a Monoclonal Cell Population by Limiting Dilution
TypeProtocol...well in sparse/individual cultures due to lack of secreted growth factors, so not every cell type will be...