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anti-Human GPSM2 Antibodies:
anti-Rat (Rattus) GPSM2 Antibodies:
anti-Mouse (Murine) GPSM2 Antibodies:
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Human Polyclonal GPSM2 Primary Antibody for ICC, IF - ABIN4315933
Kotak, Busso, Gönczy: NuMA interacts with phosphoinositides and links the mitotic spindle with the plasma membrane. in The EMBO journal 2014
Show all 2 Pubmed References
Human Polyclonal GPSM2 Primary Antibody for ELISA, WB - ABIN188736
Yasumi, Sakisaka, Hoshino, Kimura, Sakamoto, Yamanaka, Ohno, Takai: Direct binding of Lgl2 to LGN during mitosis and its requirement for normal cell division. in The Journal of biological chemistry 2005
Endothelial flow mechanotransduction through the junctional complex is mediated by a specific pool of VE-cadherin (show CDH5 Antibodies) that is phosphorylated on cytoplasmic tyrosine Y658 and bound to LGN.
In mammary stem cells, the asymmetric domain of Insc bound to LGN:Galphai(GDP) suffices to drive asymmetric fate, and reverts aberrant symmetric divisions induced by p53 loss.
Data support the notion that the Galpha (show SUCLG1 Antibodies), but not Gbetagamma, arm of the Gi/o signalling is involved in TRPC4 (show TRPC4 Antibodies) activation and unveil new roles for RGS (show PITX2 Antibodies) and LGN in fine-tuning TRPC4 (show TRPC4 Antibodies) activities.
high expression of G-protein signaling modulator 2 was involved in the pathological processes of hepatocellular carcinoma through activation of the phosphatidylinositol 3-kinase/protein kinase B (show AKT1 Antibodies) signaling pathway, which may provide an attractive potential diagnostic biomarker and therapeutic target for treatment of hepatocellular carcinoma.
This mutation is predicted to abolish all four GoLoco domains in GPSM2 and this explains the bioinformatic prediction for this mutation to be functionally damaging. Full clinical and molecular accounts of the novel mutation are provided in this paper.
Kinocilium is essential for proper localization of Lgn, as well as Gai and aPKC, suggesting that cilium function plays a role in positioning of apical proteins critical for hearing.
This study determined the crystallographic structure of human Afadin (show MLLT4 Antibodies) in complex with LGN.
results fit a model whereby LGN influences interphase microtubule dynamics in endothelial cells to regulate migration, cell adhesion, and sprout extension, and reveal a novel non-mitotic role for LGN in sprouting angiogenesis
A crystal structure of Frmpd4 (show FRMPD4 Antibodies)-bound LGN in an oxidized form is also reported, although oxidation does not appear to strongly affect the interaction with Frmpd4 (show FRMPD4 Antibodies).
LGN is required for mitotic spindle rotation but not orientation maintenance.
LGN in complex with the asymmetric domain of Inscuteable, which reveals a tetrameric arrangement of intertwined molecules.
LGN and Galphai participate in a long-inferred signal that originates outside the bundle to model its staircase-like architecture, a property that is essential for direction sensitivity to mechanical deflection and hearing.
these results show a context-dependent function for LGN.
support for the hitherto untested model that Par3 (show F2RL2 Antibodies)-mInsc (show INSC Antibodies) and Galphai3 (show GNAI3 Antibodies) act cooperatively to polarize LGN and promote perpendicular divisions
LGN-TPR motifs are versatile and capable of recognizing multiple targets via diverse binding modes.
X-ray crystallography and binding studies reveal that LGN GoLoco binding motifs are potent guanine nucleotide dissociation inhibitors.
The restricted localization of NuMA (show NUMA1 Antibodies) in the lateral belt is instructive for the planar alignment of the mitotic spindle, and required for its planar maintenance.
Knocking out LGN, (the G protein regulator), randomized the orientation of normally planar neuroepithelial divisions.
Excessive LGN induces meiotic spindle organization defects by elongating the spindle and enhancing pole focusing, whereas depletion of LGN by RNA interference results in meiotic spindle deformation and chromosome misalignment.
The protein encoded by this gene belongs to a family of proteins that modulate activation of G proteins, which transduce extracellular signals received by cell surface receptors into integrated cellular responses. The N-terminal half of this protein contains 10 copies of leu-gly-asn (LGN) repeat, and the C-terminal half contains 4 GoLoco motifs, which are involved in guanine nucleotide exchange. This protein may play a role in neuroblast division and in the development of normal hearing. Mutations in this gene are associated with autosomal recessive nonsyndromic deafness (DFNB82).
G-protein signalling modulator 2 (AGS3-like, C. elegans)
, G-protein-signaling modulator 2
, mosaic protein LGN
, G-protein signaling modulator 2 (AGS3-like, C. elegans)
, G-protein signaling modulator 2 (AGS3-like)
, LGN protein
, pins homolog (Drosophia)