Application
MSN Antibody (C-term) western blot analysis in Hela cell line lysates (35ug/lane).This demonstrates the MSN antibody detected the MSN protein (arrow).| Product Name | MSN Antibody (C-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | MSN; Moesin; Membrane-organizing extension spike protein |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WB |
| WB:1:100~500 |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Alternative Names | MSN Moesin Membrane-organizing extension spike protein |
|---|---|
| Molecular Weight(MW) | 67820 Da |
| Function | Probably involved in connections of major cytoskeletal structures to the plasma membrane. May inhibit herpes simplex virus 1 infection at an early stage |
| Tissue Specificity | In all tissues and cultured cells studied. |
| Cellular Localization | Cell membrane; Peripheral membrane protein; Cytoplasmic side (By similarity). Cytoplasm, cytoskeleton (By similarity). Apical cell membrane; Peripheral membrane protein; Cytoplasmic side (By similarity). Cell projection, microvillus membrane; Peripheral membrane protein; Cytoplasmic side (By similarity). Note=Phosphorylated form is enriched in microvilli- like structures at apical membrane (By similarity). Increased cell membrane localization of both phosphorylated and non- phosphorylated forms seen after thrombin treatment |
| Entrez Gene | 4478 |
|---|---|
| Nucleotide Accession | NP_002435.1 |
Application
MSN Antibody (C-term) western blot analysis in Hela cell line lysates (35ug/lane).This demonstrates the MSN antibody detected the MSN protein (arrow).| Application Notes | WB:1:100~500 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles. |
| Storage Buffer | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
