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anti-Human MPDZ Antikörper:
anti-Mouse (Murine) MPDZ Antikörper:
anti-Rat (Rattus) MPDZ Antikörper:
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Mouse (Murine) Monoclonal MPDZ Primary Antibody für 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 Pubmed References
Mouse (Murine) Monoclonal MPDZ Primary Antibody für IF, WB - ABIN968589
Ullmer, Schmuck, Figge, Lübbert: Cloning and characterization of MUPP1, a novel PDZ domain protein. in FEBS letters 1998
Show all 2 Pubmed References
Cow (Bovine) Polyclonal MPDZ Primary Antibody für 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
two peptides (SIAPNV(-COOH) and SIVMNV(-COOH)) were identified to have considerably improved affinity with K d increase by ~tenfold relative to wild type peptide. Thus, the two peptides are considered as promising lead entities to develop therapeutic molecular agents with high efficacy and specificity to target CaMKIIalpha (zeige CAMK2 Antikörper)-MUPP1 interaction.
Phenotypic spectrum of congenital hydrocephalus (zeige FOXC1 Antikörper) is associated with 5 recessive MPDZ alleles.
The replication association of rs1324183 (MPDZ-NF1B (zeige NFIB Antikörper)) with KC in our population and the results, which are identical to those in different populations, suggest that rs1324183 (MPDZ-NF1B (zeige NFIB Antikörper)) is a common genetic risk for Keratoconus.
MUPP-1 controls the PALS-1 (zeige MPP5 Antikörper)/PATJ (zeige INADL Antikörper) complex levels at the post-translational level.
Our data strongly support the candidacy of MPDZ as a novel congenital hydrocephalus (zeige FOXC1 Antikörper) disease gene.
The data indicates potential association between variation in mpdz NMDA dependent AMPA (zeige GRIA3 Antikörper) trafficking and alcohol dependence.
Results indicate that the coxsackievirus and adenovirus receptor (zeige CXADR Antikörper) 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 (zeige INADL Antikörper)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 (zeige MT1A Antikörper)) melatonin receptor and directly regulates its G(i)-dependent signal transduction
An interaction between the human somatostatin receptor 3 (zeige SSTR3 Antikörper) and the multiple PDZ protein MUPP1 was identified.
Variants of the multiple PDZ domain (zeige INADL Antikörper) gene Mpdz may contribute to the observed inter-strain variability in opioid tolerance and opioid-induced hyperalgesia by virtue of changes in the level of their expression.
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 (zeige INADL Antikörper) 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 (zeige NRXN1 Antikörper) interaction with multi-PDZ domain protein (zeige INADL Antikörper) 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 (zeige EPRS Antikörper) reticulata is crucially involved in risk for alcohol withdrawal.
despite their terminal sequence diversity all three GABA transporter PDZ (zeige INADL Antikörper) motifs interacted with MUPP1 domain 7
Cadm1 (zeige CADM1 Antikörper) specifically interacts with Mupp1, and may form a ternary complex with Mupp1-GABBR2 (zeige GABBR2 Antikörper) in the cerebellum.
both AF6 (zeige MLLT4 Antikörper) and MUPP1 are associated with Cx36 (zeige GJD2 Antikörper)-containing interneuronal gap junctions that form electrical synapses in adult rodent brain
CaMKIIalpha (zeige CAMK2 Antikörper) interacts with MUPP1 in spermatozoa to prevents spontaneous acrosomal exocytosis.
5-HT2C R interaction with MUPP1 is dynamically regulated by phosphorylation at Ser458
These observations indicate neuronally expressed RHGF-2 is an essential RHO-1 specific RhoGEF (zeige ARHGEF11 Antikörper) that binds most strongly to MPZ-1 PDZ domain (zeige INADL Antikörper) eight and is required for wild-type C. elegans morphology and growth.
results suggest that the ARR-1-MPZ-1-DAF (zeige CD55 Antikörper)-18 complex functions to regulate DAF-2 (zeige DAF2 Antikörper) signaling in vivo and provide insight into a novel mechanism by which arrestin (zeige SAG Antikörper) is able to regulate IGF-1R (zeige IGF1R Antikörper) signaling and longevity
These studies suggest that the SER-1 (zeige JAG1 Antikörper)/MPZ-1 interaction facilitates SER-1 (zeige JAG1 Antikörper) 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.
may play a role in G-protein coupled, 5-HT2C receptor-activated phosphoinositide-linked second messenger signaling
multi-PDZ domain protein 1
, Multiple PDZ domain protein family member (mpz-1)
, multiple PDZ domain protein
, Multiple PDZ domain protein
, multiple pdz domain protein
, LOW QUALITY PROTEIN: multiple PDZ domain protein