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Comparison of Equivalence between Two Commercially Available S499-Phosphorylated FMRP Antibodies in Mice

Fragile X syndrome (FXS) develops from excessive trinucleotide CGG repeats in the 5’-untranslated region at Xq27.3 of the Fmr-1 gene, which functionally silences its expression and prevents transcription of its protein. This disorder is the most prominent form of heritable intellectual deficiency, a...

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Detalles Bibliográficos
Autores principales: Reynolds, Conner D., Smith, Gregory D., Jefferson, Taylor S., Lugo, Joaquin N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4651511/
https://www.ncbi.nlm.nih.gov/pubmed/26580204
http://dx.doi.org/10.1371/journal.pone.0143134