Use your antibodies-online credentials, if available.
Il n’y a pas de produits dans votre liste de comparaison.
Votre panier est vide.
Afficher toutes les espèces
Afficher tous les synonymes
Sélectionnez vos espèces et l'application
anti-Mouse (Murine) Anticorps:
anti-Rat (Rattus) Anticorps:
Vous arrivez à notre recherche pré-filtrée.
SPG33 protein protrudin contains hydrophobic, intramembrane hairpin domains, interacts with tubular ER proteins, and functions in ER morphogenesis by regulating the sheet-to-tubule balance and possibly the density of tubule interconnections.
findings indicate that protrudin interacts with spastin (Montrer SPAST Anticorps) and induces axon formation through its N-terminal domain. Moreover, protrudin and spastin (Montrer SPAST Anticorps) may work together to play an indispensable role in motor axon outg
Protrudin-KIF5 com (Montrer KIF5A Anticorps)plex contributes to the vesicular trans (Montrer KIF5A Anticorps)port in neurons.
protrudin regulates Rab11 (Montrer RAB11A Anticorps)-dependent membrane recycling to promote the directional membrane trafficking required for neurite formation [protrudin]
The role of ZFYVE27/protrudin in hereditary spastic paraplegia is reported.
VAP-A (Montrer VAPA Anticorps) is an important regulator both of the subcellular localization of protrudin and of its ability to stimulate neurite outgrowth.
We found that Zfyve27, which encodes protrudin, identified a subpopulation of papillary label-retaining cells (pLRCs). With Zfyve27-CreERT2 transgenic and reporter mice we generated bitransgenic animals and performed cell-lineage analysis. Post tamoxifen, Zfyve27-CreERT2 marked cells preferentially located in the upper part of the papilla.
Identification and characterization of protrudin-L, neuron-specific isoform of protrudin that promotes axonal elongation and contributes to the establishment of neuronal polarity.
Phosphoinositides differentially regulate protrudin localization through the FYVE domain [protrudin]
protrudin contributes to the regulation of ER morphology and function, and that its deregulation by mutation is a causative defect in HSP.
Protrudin and KIF5 (Montrer KIF5A Anticorps) interact in mouse brain.Protrudin-KIF5 (Montrer KIF5A Anticorps) complex contributes to the vesicular transport in neurons.
This gene encodes a protein with several transmembrane domains, a Rab11-binding domain and a lipid-binding FYVE finger domain. The encoded protein appears to promote neurite formation. A mutation in this gene has been reported to be associated with hereditary spastic paraplegia, however the pathogenicity of the mutation, which may simply represent a polymorphism, is unclear.
zinc finger, FYVE domain containing 27
, zinc finger FYVE domain-containing protein 27
, Zinc finger FYVE domain-containing protein 27