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Arfaptin (zeige ARFIP1 ELISA Kits) physically associates with Glued and other dynactin complex components in the nervous system of both flies and mice and colocalizes with Glued at the Golgi in motor neurons.
It uncovered an important requirement for Lis1 (zeige PAFAH1B1 ELISA Kits) in promoting the recruitment of dynein and its accessory complex dynactin to RNA localization complexes.
multiple independent disruptions of Dynactin function cause a relocation of the photoreceptor nucleus toward the brain
dynein-dynactin, abnormal spindle protein (Asp (zeige ASIP ELISA Kits)), and KLP10A (zeige KIF24 ELISA Kits) have roles in Drosophila spindle pole organization
We conclude that Lis1 (zeige PAFAH1B1 ELISA Kits)/dynactin act together to regulate multiple, independent functions in mitotic cells, including spindle formation and cell cycle checkpoint release.
Microtubule binding depends on the N-terminal domain of p150[glued].
Mutants in the Lis1 (zeige PAFAH1B1 ELISA Kits)/dynactin complex strongly decrease maximum and average spindle velocity, consistent with this motor complex mediating spindle/cortex forces.
Dynein-dynactin plays a role in excluding dendritic Dscam (zeige DSCAM ELISA Kits) from axons by retrograde transport.
show that this cell polarity regulator interacts with Glued during central synapse formation.
Results suggested that variants in DCTN1 are not common risk factors for Chinese sporadic amyotrophic lateral sclerosis and that the frequency of variants of unknown significance in the cohort study was 0.39%.
This work reveals the structural details of Hook3 (zeige HOOK3 ELISA Kits)'s interaction with dynein and offers insight into how cargo adaptors form processive dynein-dynactin motor complexes.
No DCTN1 variants of disease significance were identified in this study suggesting the dynactin genes are unlikely to be a common cause of inherited peripheral neuropathies.
Mutations in the Dynactin 1 (DCTN1) gene have been demonstrated to result in various neurodegenerative diseases, including distal hereditary motor neuropathy type 7B. In the present study, a p.G59S mutation was identified as the underlying cause of Distal hereditary motor neuropathy type 7B in two families, and their detailed clinical features were characterized.
Study found that in peripheral blood mononuclear cells the median expression of KIFC3 (zeige KIFC3 ELISA Kits), KIF1B (zeige KIF1B ELISA Kits), and KIF5C was much lower than the expression of dynactin subunits DCTN1 and DCTN3 (zeige Dctn3 ELISA Kits), in both sporadic amyotrophic lateral sclerosis and healthy cases
Data suggest that cargo concentration at ERES is regulated by p150(glued) to coordinate protein sorting and transport carrier formation with the subsequent long-range transport towards the Golgi complex along microtubules.
Study shows p150glued located at the centrosome in a cell cycle-dependent manner where it is abundant during G1/S phase, located in the minus-end of microtubules during G2/M phase and at the minus-end of microtubules in the mitotic phase.
We find that LRRK1-mediated phosphorylation of CLIP-170 (zeige CLIP1 ELISA Kits) causes the accumulation of p150(Glued) (also known as DCTN1) a subunit of dynactin, at microtubule plus ends, thereby facilitating the migration of EGFR (zeige EGFR ELISA Kits)-containing endosomes.
The results describe the mutant dynactin p150Glued mouse model of motor neuron disease and show that genetic background influences phenotype in part through a region of chromosome 17 supporting the presence of genetic modifiers.
Dynactin functions as both a dynamic tether and brake during dynein-driven motility.
a mouse model expressing disease linked-G59S mutant dynactin p150(Glued) develops motor dysfunction >8 months before loss of motor neurons or dopaminergic degeneration is observed.
These findings uncovered the surprising functional relevance of GTP-bound Arl3 and LC8 for the unloading regulation of dynactin-bound cargo from dynein motor.
Functional relationships between PIK3C3 (zeige PIK3C3 ELISA Kits), dynactin, and AnkB (zeige ANKH ELISA Kits) promote axonal transport of organelles and are required for normal axon length.
The direct binding of the dynactin subunit p150(Glued) to JIP1 (zeige MAPK8IP1 ELISA Kits) competitively inhibits KHC (zeige KIF5A ELISA Kits) activation in vitro and disrupts the transport of APP (zeige APP ELISA Kits) in neurons.
These data unveil a previously unrecognized role for the dynein-dynactin motor complex in osteoclast formation and function.
in addition to its ciliogenic roles, Kif3a (zeige KIF3A ELISA Kits) recruits p150(Glued) to the subdistal appendages of mother centrioles, critical for centrosomes to function as microtubule-organizing centres.
Overexpression of TBCB leads to the decreased localization of p150 (zeige ABL1 ELISA Kits) to the microtubule network that might result in a functional modulation of this protein complex.
Melanoregulin interacts with the C-terminal domain of Rab-interacting lysosomal protein (RILP (zeige RILP ELISA Kits)) and forms a complex with RILP (zeige RILP ELISA Kits) and p150(Glued) (also known as dynactin subunit 1, DCTN1), a component of the dynein-dynactin motor complex.
It was shown KASH5 possesses hitherto unknown KASH-related sequences that directly interacted with SUN1 (zeige SUN1 ELISA Kits) and mediated telomere localization. KASH5 interacted with the microtubule-associated dynein- dynactin complex.
Dctn1 plays an important role in mouse spermiogenesis, and mainly affects the formation of the tail of spermatozoa.
This gene encodes the largest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. Dynactin is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit interacts with dynein intermediate chain by its domains directly binding to dynein and binds to microtubules via a highly conserved glycine-rich cytoskeleton-associated protein (CAP-Gly) domain in its N-terminus. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause distal hereditary motor neuronopathy type VIIB (HMN7B) which is also known as distal spinal and bulbar muscular atrophy (dSBMA).
dynactin 1 (p150, glued homolog, Drosophila)
, dynactin P150
, dynactin 1
, dynactin subunit 1
, dynactin subunit 1-like
, 150 kDa dynein-associated polypeptide
, dynactin 1, retrograde axonal transport
, dynactin 1 (p150, glued homolog)