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The results from this analysis indicated that Rab11a (zeige RAB11A ELISA Kits), Rab11c(Rab25 (zeige RAB25 ELISA Kits)) and Rab14 were expressed in a wide range of cell lines, including the human placental trophoblastic BeWo cell line.
acst as oncogene (zeige RAB1A ELISA Kits) and Induces proliferation of gastric cancer cells via AKT (zeige AKT1 ELISA Kits) signaling pathway
Rab14-specific siRNA-induced downregulation of Rab14 increases the sensitivity to cisplatin, while forced expression of Rab14 lacking 3'-UTR (zeige UTS2R ELISA Kits) abrogated the pro-apoptotic function of miR (zeige MLXIP ELISA Kits)-148a in renal cancer cells. miR (zeige MLXIP ELISA Kits)-148a acts as a tumor suppressor and holds great potential for renal cancer therapy by directly targeting Rab14.
PKCiota binds to Rab14 and that PKCiota requires Rab14 for its correct distribution in cells. As with Rab14, PKCiota protects claudin-2 (zeige CLDN2 ELISA Kits) from lysosomal degradation and, in consequence, modulates epithelial barrier.
We find that Rab14 indeed binds to RCP (zeige CRCP ELISA Kits), albeit with reduced affinity relative to conventional Rab11 (zeige RAB11A ELISA Kits)-FIP (zeige USF2 ELISA Kits) and Rab25 (zeige RAB25 ELISA Kits)-FIP (zeige USF2 ELISA Kits) complexes. However, in vivo, Rab11 (zeige RAB11A ELISA Kits) recruits RCP (zeige CRCP ELISA Kits) onto biological membranes.
RAB14 is a direct target of both MIR144 and MIR451. As MIR144 and MIR451 expression increased during human erythropoiesis, RAB14 protein expression decreased. RAB14 as a novel physiological inhibitor of human erythropoiesis.
the miR (zeige MLXIP ELISA Kits)-451/RAB14 interaction plays an important role in the enhancement of radiosensitivity in NPC (zeige NPC1 ELISA Kits) cells.
Data indicate that myosin Va (zeige MYO5A ELISA Kits) interacted with multiple new Rab (zeige HRB ELISA Kits) subfamilies including Rab6 (zeige RAB6A ELISA Kits), Rab14 and Rab39B (zeige RAB39B ELISA Kits).
Rab5a (zeige RAB5A ELISA Kits), Rab8a (zeige RAB8A ELISA Kits) and Rab14 are major regulators of MT1-MMP (zeige MMP14 ELISA Kits) trafficking and invasive migration of primary human macrophages.
Data indicate taht the parasitophorous vacuole (PV), marked with Rab14, Rab30, or Rab43, colocalize with host-derived sphingolipids in the vacuolar space.
findings provide compelling evidence that Rab22a plays a central role in the MHC-I endocytic trafficking, which is crucial for efficient cross-presentation by dendritic cells
Rab14 limits the sorting of Glut4 (zeige SLC2A4 ELISA Kits) from endosomes into insulin (zeige INS ELISA Kits)-sensitive regulated secretory compartments in adipocytes.(
Rab14 activity promotes phagosome maturation during C. albicans infection but is dysregulated on the phagosome in the presence of the invasive hyphal form, which favors fungal survival and escape.
RAB14 functions upstream of RAB10 (zeige RAB10 ELISA Kits) in the sorting of GLUT4 (zeige SLC2A4 ELISA Kits) to the specialized transport vesicles that ferry GLUT4 (zeige SLC2A4 ELISA Kits) to the plasma membrane.
the primary role of Rab14 in GLUT4 (zeige SLC2A4 ELISA Kits) trafficking is to control the transit of internalised GLUT4 (zeige SLC2A4 ELISA Kits) from early endosomes into the Golgi complex, rather than direct GLUT4 (zeige SLC2A4 ELISA Kits) translocation to the plasma membrane.
Data show that Rinl is closely associated with the cytoskeleton and thus contributes to the spatial control of Rab5a and Rab22 signaling at actin-positive compartments.
The kinesin-3 motor KIF16B (zeige KIF16B ELISA Kits)/Rab14 complex acts in biosynthetic Golgi-to-endosome traffic of the fibroblast growth factor receptor (FGFR) during early embryonic development.
Rab14 enables mycobacterial phagosomes to maintain early endosomal characteristics and avoid late endosomal/lysosomal degradative components.
The complete coding sequences of three porcine genes--RAB14, S35A3 and ITM2A (zeige ITM2A ELISA Kits) were amplified and nucleotide sequence and tissue expression were analysed.
RAB14 belongs to the large RAB family of low molecular mass GTPases that are involved in intracellular membrane trafficking. These proteins act as molecular switches that flip between an inactive GDP-bound state and an active GTP-bound state in which they recruit downstream effector proteins onto membranes (Junutula et al., 2004
RAB14, member RAS oncogene family
, rab14, member ras oncogene family
, Ras-related protein Rab-14
, ras-related protein Rab-14
, F protein-binding protein 1
, bA165P4.3 (member RAS oncogene family)
, small GTP binding protein RAB14
, GTPase Rab14
, RAB22, member RAS oncogene family
, ras-related protein Rab-22A