Titlebook: Basic DNA and RNA Protocols; Adrian J. Harwood Book 1996 Humana Press 1996

Lament

exorbitant

CBC471

Myeloproliferative Neoplasms (MPNs)this range, fragments are both difficult to separate and hard to visualize because of diffusion within the gel matrix. These problems are solved by native polyacrylamide gel electrophoresis (PAGE). Using native PAGE, fragments as small as 10 bp and up to 1 kb can be separated with a resolution of as

ENDOW

表示向下

Techniques in Molecular Hematology, to visualize by ethidium bromide staining. This can be a serious problem when separating small fragments by polyacrylamide gel electrophoresis (..). End-labeling has the second advantage that it can be used to produce fragments labeled at one end. Because all of the enzymes employed are specific to

FLASK

DEBT

https://doi.org/10.1007/978-3-642-82734-1in RNA quantity following developmental or physiological changes. Its disadvantage is that it cannot be used when the RNA sample contains additional homologous sequences, which will hybridize to the probe and confuse the results.

Emmenagogue

凹處

Basic DNA and RNA Protocols978-1-59259-251-7Series ISSN 1064-3745 Series E-ISSN 1940-6029

托運(yùn)