• Western blot analysis of lysates from HUVEC cells treated with IFN-alpha 1000U/ml 18h, using Merlin (Phospho-Ser518) Antibody. The lane on the right is blocked with the phospho peptide.
  • Western blot analysis of HELA using p-NF2 (S518) antibody. Antibody was diluted at 1:1000

Anti-Phospho-NF2-Ser518 antibody (485-534 aa) (STJ90340)

SKU:
STJ90340

Current Stock:
Host: Rabbit
Applications: WB/IHC/IF/ELISA
Reactivity: Human/Mouse/Rat
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Rabbit polyclonal antibody anti-Phospho-Merlin-Ser518 (485-534 aa) is suitable for use in Western Blot, Immunohistochemistry, Immunofluorescence and ELISA research applications.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: Liquid in PBS containing 50% Glycerol, 0.5% BSA and 0.02% Sodium Azide.
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/mL
Dilution Range: WB 1:500-1:2000
IHC 1:100-1:300
IF 1:200-1:1000
ELISA 1:5000
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Gene Symbol: NF2
Gene ID: 4771
Uniprot ID: MERL_HUMAN
Immunogen Region: 485-534 aa
Specificity: Phospho-NF2 (S518) Polyclonal Antibody detects endogenous levels of NF2 protein only when phosphorylated at S518.
Immunogen: The antiserum was produced against synthesized peptide derived from the human Merlin around the phosphorylation site of Ser518 at the amino acid range 485-534
Post Translational Modifications Phosphorylation of Ser-518 inhibits nuclear localization by disrupting the intramolecular association of the FERM domain with the C-terminal tail. The dephosphorylation of Ser-518 favors the interaction with NOP53. Ubiquitinated by the CUL4A-RBX1-DDB1-DCAF1/VprBP E3 ubiquitin-protein ligase complex for ubiquitination and subsequent proteasome-dependent degradation.
Function Probable regulator of the Hippo/SWH (Sav/Wts/Hpo) signaling pathway, a signaling pathway that plays a pivotal role in tumor suppression by restricting proliferation and promoting apoptosis. Along with WWC1 can synergistically induce the phosphorylation of LATS1 and LATS2 and can probably function in the regulation of the Hippo/SWH (Sav/Wts/Hpo) signaling pathway. May act as a membrane stabilizing protein. May inhibit PI3 kinase by binding to AGAP2 and impairing its stimulating activity. Suppresses cell proliferation and tumorigenesis by inhibiting the CUL4A-RBX1-DDB1-VprBP/DCAF1 E3 ubiquitin-protein ligase complex.
Protein Name Merlin
Moesin-Ezrin-Radixin-Like Protein
Neurofibromin-2
Schwannomerlin
Schwannomin
Database Links Reactome: R-HSA-2029482
Reactome: R-HSA-5627123
Cellular Localisation Isoform 1: Cell Projection
Filopodium Membrane
Peripheral Membrane Protein
Cytoplasmic Side
Cell Projection
Ruffle Membrane
Nucleus
In A Fibroblastic Cell Line
Isoform 1 Is Found Homogeneously Distributed Over The Entire Cell
With A Particularly Strong Staining In Ruffling Membranes And Filopodia
Colocalizes With Mpp1 In Non-Myelin-Forming Schwann Cells
Binds With Dcaf1 In The Nucleus
The Intramolecular Association Of The Ferm Domain With The C-Terminal Tail Promotes Nuclear Accumulation
The Unphosphorylated Form Accumulates Predominantly In The Nucleus While The Phosphorylated Form Is Largely Confined To The Non-Nuclear Fractions
Isoform 7: Cytoplasm
Perinuclear Region
Cytoplasmic Granule
Observed In Cytoplasmic Granules Concentrated In A Perinuclear Location
Isoform 7 Is Absent From Ruffling Membranes And Filopodia
Isoform 9: Cytoplasm
Isoform 9 Is Absent From Ruffling Membranes And Filopodia
Isoform 10: Nucleus
Cytoplasm
Cytoskeleton
Isoform 10 Is Found Homogeneously Distributed Over The Entire Cell
Alternative Antibody Names Anti-Merlin antibody
Anti-Moesin-Ezrin-Radixin-Like Protein antibody
Anti-Neurofibromin-2 antibody
Anti-Schwannomerlin antibody
Anti-Schwannomin antibody
Anti-NF2 antibody
Anti-SCH antibody

Information sourced from Uniprot.org

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