Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
NF2 encodes a protein that is similar to some members of the ERM (ezrin, radixin, moesin) family of proteins that are thought to link cytoskeletal components with proteins in the cell membrane. Additionally we are shipping Neurofibromin 2 Antibodies (161) and Neurofibromin 2 Proteins (7) and many more products for this protein.
Showing 4 out of 13 products:
Mutation of nf2 gene develops extrahepatic choledochal cysts in the common bile duct
loss of axonal contact following nerve injury results in merlin phosphorylation leading to increased p75(NTR (show NGFR ELISA Kits)) expression.
Loss of Nf2 and Cdkn2a/b have synergistic effects with PDGF-B (show PDGFB ELISA Kits) overexpression promoting meningioma malignant transformation.
Merlin 1 and 2 act as tumor suppressors and are required for optimal sperm maturation
Together our results uncover miRNAs as yet another negative mechanism controlling Merlin tumor suppressor functions.
Merlin and Ezrin (show EZR ELISA Kits) are components of a mechanism where mechanical forces associated with cell junctions are transduced across the cell cortex via cortical actomyosin cytoskeleton to control lateral mobility and activity of epidermal growth factor receptor (show EGFR ELISA Kits).
The study describe a novel NF2 mouse model recapitulating schwannoma phenotypes found in human patients where tumors develop in the cranial nerve VIII (show COX8A ELISA Kits) and/or the spinal roots.
Nf2/Merlin controls spinal cord neural progenitor function in a Rac1/ErbB2 (show ERBB2 ELISA Kits)-dependent manner.
Nf2-Yap signaling plays important roles in controlling the expansion of dorsal root ganglia progenitors and glia during DRG development
CD44 (show CD44 ELISA Kits) cytoplasmic tail cleaved by RIP (show HRB ELISA Kits) could release DCAF1 from merlin by competing for binding to the merlin FERM domain, which results in the inhibition of merlin-mediated suppression of tumorigenesis.
Findings indicate that merlin is sumoylated and that this post-translational modification is essential for tumor suppression.
NF2/merlin inactivation augments mutant RAS signaling by promoting YAP (show YAP1 ELISA Kits)/TEAD-driven transcription of oncogenic and wild-type RAS, resulting in greater MAPK (show MAPK1 ELISA Kits) output and increased sensitivity to MEK (show MAP2K1 ELISA Kits) inhibitors.
we demonstrate that NF2 negatively controls the invasiveness of Glioblastoma multiforme through YAP (show YAP1 ELISA Kits)-dependent induction of CYR61/CCN1 (show CYR61 ELISA Kits) and miR (show MLXIP ELISA Kits)-296-3p.
angiomotin and Merlin respectively interface cortical actin filaments and core kinases in Hippo signaling
(Delta2-4)Merlin variant disrupts the normal function of Merlin and promotes hepatocellular carcinoma metastasis.
Stusies indicate that monosomy 22, which is often associated with mutations of the neurofibromin 2 (NF2) gene, has emerged as the most frequent alteration of meningiomas.
NF2 (frequently deleted in MPM) inhibited Snail (show SNAI1 ELISA Kits)-mediated p53 (show TP53 ELISA Kits) suppression and was stabilized by RKIP (show PEBP1 ELISA Kits).
findings demonstrated that Merlin critically regulated pancreatic cancer pathogenesis by suppressing FOXM1 (show FOXM1 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) signaling
Mutation in NF2 gene is associated with malignant peritoneal mesothelioma.
This gene encodes a protein that is similar to some members of the ERM (ezrin, radixin, moesin) family of proteins that are thought to link cytoskeletal components with proteins in the cell membrane. This gene product has been shown to interact with cell-surface proteins, proteins involved in cytoskeletal dynamics and proteins involved in regulating ion transport. This gene is expressed at high levels during embryonic development\; in adults, significant expression is found in Schwann cells, meningeal cells, lens and nerve. Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities. Two predominant isoforms and a number of minor isoforms are produced by alternatively spliced transcripts.
neurofibromin 2 (bilateral acoustic neuroma)
, neurofibromatosis 2
, neurofibromin 2
, moesin-ezrin-radixin-like protein
, moesin-ezrin-radixin like
, moesin-ezrin-radizin-like protein