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The protein encoded by REM1 is a GTPase and member of the RAS-like GTP-binding protein family. Additionally we are shipping RAS (RAD and GEM)-Like GTP-Binding 1 Proteins (5) and many more products for this protein.
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Rad (show RRAD Antibodies), Gem (show GEM Antibodies) and Rem all reduce depolarization-dependent Ca2 (show CA2 Antibodies)+ entry in developing myotubes.
amino-termini of Rad (show RRAD Antibodies) and Rem as the structural elements dictating the specific modes of inhibition of CaV1.1 (show CACNA1S Antibodies)
Loss of an REM1 protein increased L-type calcium current density in vivo in cardiac myocytes.
both Rem and Rad (show RRAD Antibodies) bind directly to Ca2 (show CA2 Antibodies)+ channel beta-subunits (CaV (show CA5A Antibodies) beta) in vivo
We conclude that Rem is capable of regulating L-type current, that release of Rem block is modulated by cellular kinase pathways, and that the Ca(V)1.2 (show CACNA1C Antibodies) COOH terminus contributes to Rem-dependent channel inhibition.
Rem-dependent Ca2 (show CA2 Antibodies)+ channel modulation involves formation of a Rem x CaVbeta x alpha-interaction domain regulatory complex without the need to disrupt CaValpha1 x CaVbeta association or alter CaValpha1 expression at the plasma membrane.
Nuclear localization of RGK proteins (Rad (show RRAD Antibodies), Rem, and Rem2 (show REM2 Antibodies)) contributes to the suppression of RGK-mediated cell shape remodeling.
a role for the Rem C terminus in plasma membrane localization through association with phosphatidylinositol lipids.
The protein encoded by this gene is a GTPase and member of the RAS-like GTP-binding protein family. The encoded protein is expressed in endothelial cells, where it promotes reorganization of the actin cytoskeleton and morphological changes in the cells.
GTP-binding protein REM 1
, RAS-like GTP binding protein Rem
, rad and Gem-like GTP-binding protein 1
, GTPase-regulating endothelial cell sprouting
, rad and gem related GTP binding protein 1