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may play a role in G-protein coupled, 5-HT2C receptor-activated phosphoinositide-linked second messenger signaling [RGD, Feb 2006]..
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Human Polyclonal MPDZ Primary Antibody for IHC, WB - ABIN350501
Dephoure, Zhou, Villén, Beausoleil, Bakalarski, Elledge, Gygi: A quantitative atlas of mitotic phosphorylation. in Proceedings of the National Academy of Sciences of the United States of America 2008
Show all 5 references for ABIN350501
Mouse (Murine) Monoclonal MPDZ Primary Antibody for IF, WB - ABIN968588
Fallon, Moreau, Croft, Labib, Gu, Fon: Parkin and CASK/LIN-2 associate via a PDZ-mediated interaction and are co-localized in lipid rafts and postsynaptic densities in brain. in The Journal of biological chemistry 2002
Show all 2 references for ABIN968588
Human Polyclonal MPDZ Primary Antibody for IHC, WB - ABIN2775622
Szafranski, Schindler, Taudien, Hiller, Huse, Jahn, Schreiber, Backofen, Platzer: Violating the splicing rules: TG dinucleotides function as alternative 3' splice sites in U2-dependent introns. in Genome biology 2008
These observations indicate neuronally expressed RHGF-2 is an essential RHO-1 specific RhoGEF (show ARHGEF11 Antibodies) that binds most strongly to MPZ-1 PDZ domain (show INADL Antibodies) eight and is required for wild-type C. elegans morphology and growth.
results suggest that the ARR-1-MPZ-1-DAF (show CD55 Antibodies)-18 complex functions to regulate DAF-2 signaling in vivo and provide insight into a novel mechanism by which arrestin (show SAG Antibodies) is able to regulate IGF-1R (show IGF1R Antibodies) signaling and longevity
These studies suggest that the SER-1 (show JAG1 Antibodies)/MPZ-1 interaction facilitates SER-1 (show JAG1 Antibodies) mediated signaling.
This evidence points to a role of MUPP1 as a membrane raft-associated molecular organizer, suggesting that mammalian spermatozoa may use a scaffolding protein and membrane subdomains to organize components involved in the process of acrosomal exocytosis.
The replication association of rs1324183 (MPDZ-NF1B (show NFIB Antibodies)) with KC in our population and the results, which are identical to those in different populations, suggest that rs1324183 (MPDZ-NF1B (show NFIB Antibodies)) is a common genetic risk for Keratoconus.
MUPP-1 controls the PALS-1 (show MPP5 Antibodies)/PATJ (show INADL Antibodies) complex levels at the post-translational level.
Our data strongly support the candidacy of MPDZ as a novel congenital hydrocephalus (show FOXC1 Antibodies) disease gene.
The data indicates potential association between variation in mpdz NMDA dependent AMPA (show GRIA3 Antibodies) trafficking and alcohol dependence.
Results indicate that the coxsackievirus and adenovirus receptor (show CXADR Antibodies) interacts with multi-PDZ domain protein 1 (MUPP1) and is involved in MUPP1 recruitment to the tight junction.
The results revealed prominent MUPP1 expression which was (show INADL Antibodies)restricted to the apical acrosomal region and, most notably, to the equatorial segment of the acrosome[MUPP1]
MUPP1 binds to the G protein-coupled MT(1 (show MT1A Antibodies)) melatonin receptor and directly regulates its G(i)-dependent signal transduction
An interaction between the human somatostatin receptor 3 (show SSTR3 Antibodies) and the multiple PDZ protein MUPP1 was identified.
Exploratory haplotype and single nucleotide polymorphisms association analyses suggest a possible association between the MPDZ gene and alcohol dependence but not alcohol withdrawal seizures.
Results suggest that signaling mediated by Pals1 (show MPP5 Antibodies), which has a higher affinity for Patj (show INADL Antibodies) than for MUPP1 and is involved in the activation of the Par6 (show PARD6A Antibodies)-aPKC complex, is of principal importance for the function of Patj (show INADL Antibodies) in epithelial cells.
MUPP1-PDZ4 domain contained three alpha-helices and six beta-strands in the core. The GLGI motif, L562/A564 on the beta-strand B, and H605/V608/L612 on the alpha-helix B formed a PDZ (show INADL Antibodies) binding pocket which could bind to the C-terminal of the binding partners.
Increased MPDZ expression decreased the severity of ethanol withdrawal, while decreased MPDZ expression increased ethanol withdrawal severity. Decreased MPDZ expression was associated with increased voluntary ethanol consumption.
neurexin 1 (show NRXN1 Antibodies) interaction with multi-PDZ domain protein (show INADL Antibodies) MUPP1
Our results confirm that Mpdz is a quantitative trait gene for alcohol withdrawal and demonstrate that its expression in the caudolateral substantia nigra pars (show EPRS Antibodies) reticulata is crucially involved in risk for alcohol withdrawal.
despite their terminal sequence diversity all three GABA transporter PDZ (show INADL Antibodies) motifs interacted with MUPP1 domain 7
Cadm1 (show CADM1 Antibodies) specifically interacts with Mupp1, and may form a ternary complex with Mupp1-GABBR2 (show GABBR2 Antibodies) in the cerebellum.
both AF6 (show MLLT4 Antibodies) and MUPP1 are associated with Cx36 (show GJD2 Antibodies)-containing interneuronal gap junctions that form electrical synapses in adult rodent brain
CaMKIIalpha (show CAMK2 Antibodies) interacts with MUPP1 in spermatozoa to prevents spontaneous acrosomal exocytosis.
5-HT2C (show HTR2C Antibodies) R interaction with MUPP1 is dynamically regulated by phosphorylation at Ser458
MUPP1 protein expression is co-localized with 5-HT(2A (show HTR2A Antibodies)) or 5-HT(2C (show HTR2C Antibodies)) receptor expression in all regions of the mouse brain, including the choroid plexus where 5-HT(2C (show HTR2C Antibodies)) receptors are highly enriched.
may play a role in G-protein coupled, 5-HT2C receptor-activated phosphoinositide-linked second messenger signaling
Multiple PDZ domain protein family member (mpz-1)
, multiple PDZ domain protein
, Multiple PDZ domain protein
, multiple pdz domain protein
, multi-PDZ domain protein 1