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Small GTP-binding proteins of the RAB family, such as RAB32, play essential roles in vesicle and granule targeting (Bao et al., 2002 [PubMed 11784320]).[supplied by OMIM, Aug 2009].. Zusätzlich bieten wir Ihnen RAB32 Antikörper (40) und viele weitere Produktgruppen zu diesem Protein an.
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this study provides some compelling evidence showing that Rab32 is an essential host factor required for HCV particle assembly and thus that Rab32 could be a potential therapeutic target to interrupt HCV propagation.
Rab32 controls intracellular lipid accumulation through inducing lipolysis via enhancing ATGL (zeige PNPLA2 Proteine) expression indirectly.
Rab32 may regulate the physiological functions of LRRK2 (zeige LRRK2 Proteine).
Rab38 and its close homolog Rab32 bind to Myosin Vc but not to Myosin Va or Myosin Vb. Binding depends on residues in the switch II region of Rab32 and Rab38 and regions of the Myosin Vc coiled-coil tail domain.
BLOC-3 is a Rab32 and Rab38 (zeige RAB38 Proteine) guanine nucleotide exchange factor (zeige RASGRF1 Proteine), with a specific function in the biogenesis of lysosome-related organelles.
that Rab38 (zeige RAB38 Proteine) and Rab32 are the specific factors that direct the ubiquitous machinery to mediate transport from early endosomes to maturing LROs.
Identification of two new loci at IL23R (zeige IL23R Proteine) and RAB32 that influence susceptibility to leprosy
Rab32 is a dual function protein that participates in both mitochondrial anchoring of PKA and synchronization of mitochondrial fission.
RAB32 inactivation may represent a component of the oncogenic pathway of microsatellite-unstable gastrointestinal adenocarcinomas
Results suggest that Rab32 facilitates the formation of autophagic vacuoles whose membranes are derived from the ER and regulates the clearance of aggregated proteins by autophagy.
Rab32 represents a general cell-autonomous, antimicrobial defense that is counteracted by two Salmonella effectors.
Rab32 could improve the induction of iPSCs through the enhancement of lipid biosynthesis, highlighting the importance of lipid metabolism during reprogramming.
Data suggest RUTBC1/SGSM2 in melanocytes functions as physiological GTPase-activating protein for Rab32/Rab38 in regulation of transport of melanogenic enzymes (tyrosinase, tyrosinase-related protein 1, dopachrome isomerase) into melanosomes.
RNA interference-mediated depletion of Rab32 or of an essential component of a BLOC complex was sufficient to allow S. Typhi to survive within mouse macrophages.
Through a combination of its functions as a PKA-anchoring protein and a regulator of MAM properties, the activity and expression level of Rab32 determine the speed of apoptosis onset.
Data report the cloning and characterization of the mouse homologue of human Rab32.
Varp (zeige ANKRD27 Proteine) functions as the Rab32/38 effector that controls trafficking of Tyrp1 (zeige TYRP1 Proteine) in melanocytes.
Small GTP-binding proteins of the RAB family, such as RAB32, play essential roles in vesicle and granule targeting (Bao et al., 2002
RAB32, member RAS oncogene family
, ras-related protein Rab-32