ARG63977

anti-MSN / Moesin antibody

anti-MSN / Moesin antibody for Western blot and Human,Mouse

Signaling Transduction antibody

Overview

Product Description Goat Polyclonal antibody recognizes MSN / Moesin
Tested Reactivity Hu, Ms
Predict Reactivity Dog, Rat
Tested Application WB
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name MSN / Moesin
Antigen Species Human
Immunogen C-NARDESKKTAND
Conjugation Un-conjugated
Alternate Names Moesin; Membrane-organizing extension spike protein; HEL70

Application Instructions

Application Suggestion
Tested Application Dilution
WB1 - 3 µg/ml
Application Note WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by antigen affinity chromatography.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 17698 Mouse MSN

GeneID: 4478 Human MSN

Swiss-port # P26038 Human Moesin

Swiss-port # P26041 Mouse Moesin

Background Moesin (for membrane-organizing extension spike protein) is a member of the ERM family which includes ezrin and radixin. ERM proteins appear to function as cross-linkers between plasma membranes and actin-based cytoskeletons. Moesin is localized to filopodia and other membranous protrusions that are important for cell-cell recognition and signaling and for cell movement. [provided by RefSeq, Jul 2008]
Research Area Signaling Transduction antibody
Calculated MW 68 kDa
PTM Phosphorylation on Thr-558 is crucial for the formation of microvilli-like structures. Phosphorylation by ROCK2 suppresses the head-to-tail association of the N-terminal and C-terminal halves resulting in an opened conformation which is capable of actin and membrane-binding (By similarity). Phosphorylation on Thr-558 by STK10 negatively regulates lymphocyte migration and polarization.
S-nitrosylation of Cys-117 is induced by interferon-gamma and oxidatively-modified low-densitity lipoprotein (LDL(ox)) implicating the iNOS-S100A8/9 transnitrosylase complex.