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anti-Human ARPC3 Antibodies:
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Human Monoclonal ARPC3 Primary Antibody for ICC, ELISA - ABIN1742555
Gonzalez-Aparicio, Flores, Fernandez-Espejo: Antiparkinsonian trophic action of glial cell line-derived neurotrophic factor and transforming growth factor β1 is enhanced after co-infusion in rats. in Experimental neurology 2010
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Cow (Bovine) Polyclonal ARPC3 Primary Antibody for WB - ABIN2784768
Ewing, Chu, Elisma, Li, Taylor, Climie, McBroom-Cerajewski, Robinson, OConnor, Li, Taylor, Dharsee, Ho, Heilbut, Moore, Zhang, Ornatsky, Bukhman, Ethier, Sheng, Vasilescu, Abu-Farha, Lambert, Duewel et al.: Large-scale mapping of human protein-protein interactions by mass spectrometry. ... in Molecular systems biology 2007
Human Polyclonal ARPC3 Primary Antibody for ELISA, WB - ABIN185223
Welch, DePace, Verma, Iwamatsu, Mitchison: The human Arp2/3 complex is composed of evolutionarily conserved subunits and is localized to cellular regions of dynamic actin filament assembly. in The Journal of cell biology 1997
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Cancer cell motility mediated by the actin-related protein 2 (show ACTR2 Antibodies)/3 complex (Arp2 (show ACTR2 Antibodies)/3) is required for vessel co-option in liver metastases in vivo.
genetic association study in population in Canada: Data suggest that an SNP in the promoter region of ARPC3 (CpG-SNP rs3759384 C>T) is associated with metabolic syndrome complicated by severe abdominal obesity and hypertriglyceridemia in the population studied.
Endogenous Nogo-B (show RTN4 Antibodies), which may exert its effects through ARPC 2 (show ARPC2 Antibodies)/3 and MYL-9 (show MYL9 Antibodies), is necessary for the migration and contraction of airway smooth muscle cells.
The actin-related protein 3 (show ACTR3 Antibodies) structures were more visible with anti-p34Arc monoclonal antibody.
This study provided the first evidence that the Arp2/3 complex, a key actin nucleator, is involved in distinct stages of spine formation and is required for synapse unsilencing.
In the absence of ArpC3, enterocytes had defects in the organization of the endolysosomal system: transcytosis of IgG was disrupted, lipid absorption was perturbed, and neonatal mice died within days of birth.
GMF debranches filaments by a mechanism related to cofilin-mediated severing, but in which GMF has evolved to target molecular junctions between actin-related proteins in the Arp2/3 complex and actin subunits in the daughter filament of the branch.
Together with the observation that Gadkin-mediated inhibition of cell spreading requires its binding to ARP2 (show AICDA Antibodies)/3, these data indicate that Gadkin is a negative regulator of ARP2 (show AICDA Antibodies)/3 function present on intracellular membranes
results demonstrate a critical role for the Arp2 (show AICDA Antibodies)/3 complex in the assembly of lamellipodia-based leading edges and directional cell motility
that targeting of Arpc3 by miR-29a/b fine tunes structural plasticity by regulating actin network branching in mature and developing spines
These data indicate the importance of Arpc3 in the Arp2 (show AICDA Antibodies)/3 complex for trophoblast outgrowth and suggest that Arpc3 may be indispensable for implantation.
The GMF-Arp2 interface reveals how the ADF-H actin-binding domain in GMF is exploited to specifically recognize Arp2/3 complex and not actin.
This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been implicated in the control of actin polymerization in cells and has been conserved through evolution. The exact role of the protein encoded by this gene, the p21 subunit, has yet to be determined.
ARP2/3 protein complex subunit p21
, actin-related protein 2/3 complex subunit 3
, arp2/3 complex 21 kDa subunit
, Arp2/3 complex subunit p21-Arc
, actin related protein 2/3 complex subunit 3
, actin related protein 2/3 complex, subunit 3, 21kDa