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The protein encoded by GPSM2 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. Additionally we are shipping GPSM2 Proteins (4) and many more products for this protein.
Showing 10 out of 53 products:
Chicken Polyclonal GPSM2 Primary Antibody for IF, IHC - ABIN2784504
Izaki, Kamakura, Kohjima, Sumimoto: Two forms of human Inscuteable-related protein that links Par3 to the Pins homologues LGN and AGS3. in Biochemical and biophysical research communications 2006
Human Polyclonal GPSM2 Primary Antibody for ELISA, WB - ABIN190875
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
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.
Hepatocyte Par1b (show MARK2 Antibodies) defines lumen position in concert with the position of the astral microtubule anchoring complex LGN-NuMA (show NUMA1 Antibodies) to yield the distinct epithelial division phenotypes.
one homozygous frameshift GPSM2 variants c.1473delG was identified in three Chudley-McCullough syndrome Dutch patients.
Data indicate that dynein- and astral microtubule-mediated transport of Galphai/LGN/nuclear mitotic apparatus (NuMA (show NUMA1 Antibodies)) complex from cell cortex to spindle poles.
Studies indicate that the Inscuteable (Insc (show INSC Antibodies))and NuMA (show NUMA1 Antibodies) are mutually exclusive interactors of LGN.
Results show compound heterozygous mutations in the GPSM2 gene, in affected members of a family with Chudley-McCullough syndrome, co-segregate in the family as an autosomal recessive trait.
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)