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Members of the Rab protein family, including RAB27B, are prenylated, membrane-bound proteins involved in vesicular fusion and trafficking (Chen et al., 1997 [PubMed 9066979]).[supplied by OMIM, Nov 2010].. Additionally we are shipping RAB27B Antibodies (67) and RAB27B Proteins (13) and many more products for this protein.
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Rab27b enrichment occurs early in secretory vesicle formation.
Rab27b participates in aspects of lacrimal gland acinar cell secretory vesicle formation and release.
Rab27b is associated with tubulovesicle membranes in the parietal cell and Rab27b may play a role in stimulation-associated membrane recruitment and gastric acid secretion.
RAB27A (show RAB27A ELISA Kits), RAB27B and VPS36 (show VPS36 ELISA Kits) are frequently underexpressed in advanced prostate cancer and are inversely correlated with prostate cancer outcome. There seems to be a close relationship in the expression of RAB27A (show RAB27A ELISA Kits), RAB27B and VPS36 (show VPS36 ELISA Kits), with RAB27A (show RAB27A ELISA Kits) and RAB27B being dependent on VPS36 (show VPS36 ELISA Kits).
decreased expression of Rab27A (show RAB27A ELISA Kits) and Rab27B, especially Rab27A (show RAB27A ELISA Kits), closely correlated with tumor progression and are valuable prognostic indicators in colorectal cancer patients.
Data indicate that a significant correlation between rab (show HRB ELISA Kits) GTP-binding protein (RAB27B) and p53 tumor suppressor protein (p53 (show TP53 ELISA Kits)) expression was observed.
MiR (show MLXIP ELISA Kits)-193a-3p and miR (show MLXIP ELISA Kits)-193a-5p play important roles in osteosarcoma metastasis through down-regulation of the Rab27B and SRR (show SRR ELISA Kits) genes and therefore may serve as useful biomarkers for the diagnosis of osteosarcoma
These data indicate that Rab27B is involved at a different steps of zymogen granule maturation and secretion, which is distinct from that of Rab3D (show RAB3D ELISA Kits).
Experimental data are reviewed with a focus on the secretory Rab27 (show RAB27A ELISA Kits) family of small GTPases and their implications in cancer progression.
Decreased invasion partly resulted from reduced expression and activation of MMP-9 (show MMP9 ELISA Kits) after Rab27b knockdown. Downregulation of Rab27b also suppressed tumor growth in vivo.
Data indicate that the secretion of microRNA miR (show MLXIP ELISA Kits)-143, depends on rab (show HRB ELISA Kits) GTP-binding (show RND2 ELISA Kits) proteins Rab7a (show RAB7A ELISA Kits) and Rab27b.
Rab27B nuclear expression is correlated with several clinicopathological features of GIST patients, and it may serve as an unfavorable prognostic marker.
Silencing of the exocytotic RAB (show HRB ELISA Kits) family members RAB27A (show RAB27A ELISA Kits) or RAB27B halted miR23b and miR921 secretion and reduced cellular invasion.
PI3K-dependent formation of a kinesin-1/Slp3/Rab27b complex is critical for the microtubule-dependent movement of secretory granules required for mast cell degranulation.
Loss of Rab3D (show RAB3D ELISA Kits) from secretory vesicles, leading to disproportionate Rab27 (show RAB27A ELISA Kits)-to-Rab3D (show RAB3D ELISA Kits) activity, may contribute to the enhanced release of cathepsin S (show CTSS ELISA Kits) in tears of patients with Sjogren's syndrome.
Rab27b is expressed in bone marrow derived neutrophils and Rab27b knockout (Rab27b KO) along with Rab27a/b (show RAB27A ELISA Kits) double knockout (Rab27DKO) neutrophils exhibit impaired transwell migration in vitro in response to chemokines MIP-2 (show CXCL2 ELISA Kits) and LTB4 (show PTGR1 ELISA Kits).
EPI64B (show TBC1D10B ELISA Kits) can serve as a potential physiological GAP for Rab27B and thereby participate in the regulation of exocytosis in pancreatic acinar cells.
Expression of Rab27b DN constructs resulted in dispersed collagen vesicles which may represent failed secretory vesicles sequestered in the cytosol.
Data suggest that Rab27a (show RAB27A ELISA Kits) and Rab27b regulate distinct steps in the bone marrow-derived mast cells (BMMC) degranulation pathway, with Rab27a (show RAB27A ELISA Kits)/Mlph (show MLPH ELISA Kits)/MyoVa (show MYO5A ELISA Kits) regulating cortical actin stability upstream of Rab27a/b (show RAB27A ELISA Kits)/Munc13-4 (show UNC13D ELISA Kits)-dependent granule exocytosis.
Data indicate that inhibition of Rab27a (show RAB27A ELISA Kits), but not Rab27b, affects exosome secretion.
Stimulation-dependent lysosomal RANKL (show TNFSF11 ELISA Kits) release is mediated by Rab27a/b (show RAB27A ELISA Kits) and their effector molecules, and this mechanism may be important for osteoclast activation in vivo.
Morphological changes observed at the ultrastructural level in Rab27b-deficient lung samples result from secretory defects in alveolar epithelial type II and Clara cells that, over time, lead to atrophy of the epithelium.
Members of the Rab protein family, including RAB27B, are prenylated, membrane-bound proteins involved in vesicular fusion and trafficking (Chen et al., 1997
RAB27B, member RAS oncogene family
, ras-related protein Rab-27B