Ribosomal Protein L26L Polyclonal Antibody, 100ul Plasma but it localizes to unique

but it localizes to unique cap structures at the nucleolar periphery when RNA polymerase II transcription is inhibited

hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11

and this protein is 100% identical to the rat ortholog

Mutations in this gene are associated with inherited venous malformations of the skin and mucous membranes

which is located in the third intron

Ribosomal Protein L26L Polyclonal Antibody, 100ul Plasma but it localizes to uniqueRPL26L1 encodes a protein that shares high sequence similarity with ribosomal protein L26. Alternative splicing results in multiple transcript variants encoding the same protein.