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FEZ1 is an ortholog of the C. Zusätzlich bieten wir Ihnen FEZ1 Antikörper (62) und viele weitere Produktgruppen zu diesem Protein an.
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FEZ1 (zeige LZTS1 Proteine) promotes HIV-1 infection in non-neuronal cells via direct binding to the capsid and kinesin-1 to move the virus into the cell nucleus.
SCOC (zeige SCOC Proteine) forms a stable homogeneous complex with the coiled coil domain of FEZ1 (zeige LZTS1 Proteine). SCOC (zeige SCOC Proteine) dimerization and the SCOC (zeige SCOC Proteine) surface residue R117 are important for this interaction.
Studies indicate that FEZ1 (fasciculation and elongation protein zeta 1 (zeige LZTS1 Proteine)), SCOCO (short coiled-coil protein (zeige SCOC Proteine)) and kinesins (kinesin heavy chain (zeige KIF5A Proteine)) are involved in biological transport process.
Short Disrupted-in-Schizophrenia (DISC)1 splice variants show reduced or no binding to NDEL1 and phosphodiesterase (PDE)4B proteins but fully interact with FEZ1 and GSK3beta.
FEZ1 (zeige LZTS1 Proteine) operates as a kinesin adaptor for the transport of Stx (zeige ST8SIA2 Proteine), with cargo loading and unloading being regulated by protein kinases.
The data of this study suggested that FEZ1 (zeige LZTS1 Proteine) may play important roles in human astrocytes, and that mood stabilizers might exert their cytoprotective and mood-stabilizing effects by inducing FEZ1 (zeige LZTS1 Proteine) expression in astrocytes.
Genetic association analysis of two independent cohorts of (zeige DISC1 Proteine)schizophrenia patients and healthy controls reveals an epistatic interaction between FEZ1 and disrupted in schizophrenia (DISC)1.
FEZ2 (zeige FEZ2 Proteine) interacted with 59 proteins and that of these only 40 interacted with FEZ1 (zeige LZTS1 Proteine).
Demonstrated the formation of an intermolecular disulfide bond through FEZ1 (zeige LZTS1 Proteine) Cys (zeige DNAJC5 Proteine)-133, which appears to be essential for dimerization.
Studies indicate that suppression of FEZ1 (zeige LZTS1 Proteine) expression in cultured embryonic neurons causes deficiency of neuronal differentiation.
Phosphorylation of FEZ1 by MARK regulates its function in presynaptic protein trafficking.
Dendrite growth depends on degradation of FEZ1 regulated by Cdc20 (zeige CDC20 Proteine)/APC (zeige APC Proteine).
Fezzeta-1 interacts with disrupted in schizophrenia (DISC)1 (zeige DISC1 Proteine) to synergistically regulate dendritic growth of newborn neurons in the adult mouse hippocampus.
Fez1 is mainly expressed in cortical layers V and VI, not in gamma-aminobutyric acid neurons but in pyramidal neurons, the projection neurons of the cerebral cortex. Immunohistochemistry also shows that Fez1 is expressed in deep layers of the neocortex.
investigated the role of FEZ1 in brain development and the pathogenesis of schizophrenia by generating mice that lack Fez1
fez1 (zeige LZTS1 Proteine) is crucial for establishing regional subdivisions within the diencephalon and may also play a role in the development of the telencephalon and hypothalamus.
This gene is an ortholog of the C. elegans unc-76 gene, which is necessary for normal axonal bundling and elongation within axon bundles. Expression of this gene in C. elegans unc-76 mutants can restore to the mutants partial locomotion and axonal fasciculation, suggesting that it also functions in axonal outgrowth. The N-terminal half of the gene product is highly acidic. Alternatively spliced transcript variants encoding different isoforms of this protein have been described.
fasciculation and elongation protein zeta-1
, zygin I
, protein kinase C-binding protein Zeta1
, zygin 1
, fasciculation and elongation protein zeta 1 (zygin I)
, fasciculation and elongation protein zeta 1 L homeolog