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primary structure was determined and developmental regulation of the gene (ATP1B4) was analyzed
During evolution, ATP1B4 lost its ancestral function, accumulated in nuclear membrane of perinatal myocytes, and associates with transcriptional coregulator Ski-inte (show EIF3K ELISA Kits)racting protein (SKIP).
variant in the coding region of the ATP1B4 gene may play little or no role in the development of PD in Chinese Han population.
Radical changes in the functions of orthologous ATP1B4 genes occurred during evolution of vertebrates. Expression of the ATP1B4 gene is predominantly muscle-specific (show EIF3K ELISA Kits) in tetrapods.
This gene has been found in all vertebrate genomes sequenced to date. However, this gene has undergone a change in function in placental mammals compared to other species. Specifically, in fish, avian, and amphibian species, this gene encodes plasma membrane-bound beta-subunits of Na,K-ATPase. In placental mammals, the encoded protein interacts with the nuclear transcriptional coregulator SKIP and may be involved in the regulation of TGF-beta signaling. Two transcript variants encoding different isoforms have been found for this gene.
, x,K-ATPase subunit beta-m
, x/potassium-transporting ATPase subunit beta-m
, Na,K-ATPase beta m-subunit
, X,K-ATPase beta-m subunit
, ATPase, (Na+)/K+ transporting, beta 4 polypeptide
, X/potassium-transporting ATPase subunit beta-m
, X,K-ATPase subunit beta-m