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These findings suggest that RalB might be one of the targets for facilitating the invasive phenotype of malignant gliomas induced by GGTase-I.
striking isoform-specific consequences of distinct CAAX-signaled posttranslational modifications that contribute to the divergent subcellular localization and activity of RalA (show rala ELISA Kits) and RalB.
expression of K-Ras (show HRAS ELISA Kits) and RalB and possibly RalA (show rala ELISA Kits) proteins is critical for maintaining low levels of p53 (show TP53 ELISA Kits), and down-regulation of these GTPases reactivates p53 (show TP53 ELISA Kits) by significantly enhancing its stability, contributing to suppression of malignant transformation
High RALB mRNA expression is associated with non-small-cell lung cancer growth and progression.
Integrin alpha(v (show ITGAV ELISA Kits))beta expression and the resulting KRAS-RalB-NF-kappaB (show NFKB1 ELISA Kits) pathway were both necessary and sufficient for tumour initiation, anchorage independence, self-renewal and erlotinib resistance.
nutrient starvation induces RALB deubiquitylation by accumulation and relocalization of the deubiquitylase USP33 (show USP33 ELISA Kits) to RALB-positive vesicles
RalA (show rala ELISA Kits) and RalB exhibit both distinct and redundant roles in tumorigenesis (Review).
The study found upregulated RalA (show rala ELISA Kits) and RalB activation in colorectal cancer tumor cell lines and tumors.
the existence of an ubiquitination/de-ubiquitination cycle superimposed on the GDP/GTP (show AK3 ELISA Kits) cycle of RalA (show rala ELISA Kits), involved in the regulation of RalA (show rala ELISA Kits) activity as well as in membrane raft trafficking.
RalA (show rala ELISA Kits) and RalB differentially regulate development of epithelial tight junctions.
findings show either RALA (show rala ELISA Kits) or RALB is sufficient for tumor growth; either RALA (show rala ELISA Kits) or RALB is sufficient for cell proliferation; RALA (show rala ELISA Kits) and RALB act in a redundant fashion
Endogenous RalB plays a negative role in the ingestion process of Fc gamma receptor (show FCGR1A ELISA Kits)-mediated macrophage phagocytosis.
This gene encodes a GTP-binding protein that belongs to the small GTPase superfamily and Ras family of proteins. GTP-binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors.
RAS-like protein B
, ras related GTP binding protein
, ras-related protein Ral-B
, v-ral simian leukemia viral oncogene homolog B (ras related; GTP binding protein)
, GTP binding protein)
, v-ral simian leukemia viral oncogene homolog B (ras related)