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anti-Human MAGI2 Antibodies:
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Dog (Canine) Polyclonal MAGI2 Primary Antibody for WB - ABIN2788791
Doukhanine, Gavino, Haines, Almazan, Richard: The QKI-6 RNA binding protein regulates actin-interacting protein-1 mRNA stability during oligodendrocyte differentiation. in Molecular biology of the cell 2010
Human Polyclonal MAGI2 Primary Antibody for ELISA - ABIN547201
Shoji, Tsuchida, Kishi, Yamakawa, Matsuzaki, Liu, Nakamura, Sugino: Identification and characterization of a PDZ protein that interacts with activin type II receptors. in The Journal of biological chemistry 2000
MAGI2-AS3 plays an important role as a tumour suppressor by targeting Fas and FasL signalling.
MAGI-2 immunoreactivity is elevated in prostate cancer and high-grade prostatic intraepithelial neoplasia compared with normal tissue, suggesting that MAGI-2 may contribute to prostate carcinogenesis.
Immunohistochemistry in kidney sections from these patients revealed that mutations resulted in lack of or diminished podocyte MAGI2 expression. Our data support the finding that mutations in the MAGI2 gene are causal for congenital steroid-resistant nephrotic syndrome
MAGI-2 could represent a useful adjunct for diagnosis of prostatic adenocarcinoma
The expression of MAGI2 mRNA was significantly down-regulated in PC3, LNCaP and DU-145 PCa cell lines.
MAGI2, SERPINE2, and NT5C3B expression levels are associated with airway wall thickening and additionally with bronchial inflammation, emphysema, and lung function, respectively, all features of chronic obstructive pulmonary disease.
Data show that the miR-134/487b/655 cluster regulates TGF-beta1-induced epithelial-mesenchymal transition and affected the resistance to gefitinib by directly targeting membrane-associated guanylate kinase, WW, and PDZ domain-containing protein 2 (MAGI2).
In Usher syndrome 1G, mutations in SANS eliminate Magi2 binding and thereby deregulate endocytosis, lead to defective ciliary transport modules and ultimately disrupt photoreceptor cell function inducing retinal degeneration.
MAGI2 enhances the sensitivity of BEL-7404 human hepatocellular carcinoma cells to staurosporine-induced apoptosis by increasing PTEN stability.
Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients.
Results presented herein provide further evidence for a role of MAGI2 in bipolar affective disorder and schizophrenia etiology.
Interstitial deletions that include the MAGI2 gene on chromosome 7q11.23-q.21.11 are associated with IS cases.
there was no association of MAGI2 and PARD3 with IBD.
analysis of 7q11.21-q11.23 and infantile spasms without deletion of MAGI2 [case report]
Data show that AIP1 is a novel GTPase-activating protein for Arf6, a small GTPase regulating cellular PIP(2) production and formation of the TLR4-TIRAP-MyD88 complex.
PTEN plays a critical role in MAGI-2-induced inhibition of cell migration and proliferation in human hepatocarcinoma cells
MAGI2 genetic variation is associated with inflammatory bowel disease.
The protein encoded by this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral and pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase-like domain, and multiple PDZ domains. It has structural similarity to the membrane-associated guanylate kinase homologue (MAGUK) family.
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2
, membrane associated guanylate kinase, WW and PDZ domain containing 2
, Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2
, membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like
, activin receptor interacting protein 1
, atrophin-1-interacting protein 1
, atrophin-1-interacting protein A
, membrane-associated guanylate kinase inverted 2
, activin receptor-interacting protein 1
, synaptic-scaffolding molecule