PDF DatasheetHuman and Rat Anti-Moesin Antibody Product Attributes
Moesin Previously Observed Antibody Staining Patterns
Observed Subcellular, Organelle Specific Staining Data:
Anti-MSN antibody staining is expected to be primarily localized to the plasma membrane.
Observed Antibody Staining Data By Tissue Type:
Variations in Moesin antibody staining intensity in immunohistochemistry on tissue sections are present across different anatomical locations. An intense signal was observed in hematopoietic cells in the bone marrow, germinal center cells in the lymph node and tonsil and non-germinal center cells in the tonsil. More moderate antibody staining intensity was present in hematopoietic cells in the bone marrow, germinal center cells in the lymph node and tonsil and non-germinal center cells in the tonsil. Low, but measureable presence of Moesin could be seen inglandular cells in the breast, cells in the molecular layer in cerebellum, glial cells in the cerebral cortex, glandular cells in the cervix, uterine, squamous epithelial cells in the cervix, uterine, cells in the endometrial stroma in endometrium, glandular cells in the endometrium and fallopian tube, follicle cells in the ovary, ovarian stroma cells in the ovary, exocrine glandular cells in the pancreas, glandular cells in the parathyroid gland, prostate and seminal vesicle, fibroblasts in skin, keratinocytes in skin, melanocytes in skin, smooth muscle cells in the smooth muscle, cells in the seminiferous ducts in testis, glandular cells in the thyroid gland and urothelial cells in the urinary bladder. We were unable to detect Moesin in other tissues. Disease states, inflammation, and other physiological changes can have a substantial impact on antibody staining patterns. These measurements were all taken in tissues deemed normal or from patients without known disease.
Observed Antibody Staining Data By Tissue Disease Status:
Tissues from cancer patients, for instance, have their own distinct pattern of Moesin expression as measured by anti-Moesin antibody immunohistochemical staining. The average level of expression by tumor is summarized in the table below. The variability row represents patient to patient variability in IHC staining.
| Sample Type | breast cancer | carcinoid | cervical cancer | colorectal cancer | endometrial cancer | glioma | head and neck cancer | liver cancer | lung cancer | lymphoma | melanoma | ovarian cancer | pancreatic cancer | prostate cancer | renal cancer | skin cancer | stomach cancer | testicular cancer | thyroid cancer | urothelial cancer |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Signal Intensity | – | – | ++ | – | + | – | +++ | + | ++ | +++ | ++ | + | ++ | – | ++ | ++ | – | + | +++ | – |
| MSN Variability | + | ++ | ++ | + | ++ | ++ | ++ | ++ | ++ | ++ | + | ++ | ++ | + | ++ | ++ | ++ | ++ | ++ | ++ |
| Moesin General Information | |
|---|---|
| Alternate Names | |
| HEL70, Moesin | |
| Molecular Weight | |
| 78kDa | |
| Chromosomal Location | |
| Xq11.1 | |
| Curated Database and Bioinformatic Data | |
| Gene Symbol | MSN |
| Entrez Gene ID | 4478 |
| Ensemble Gene ID | ENSG00000147065 |
| RefSeq Protein Accession(s) | XP_005262326, XP_011529261, XP_016885034, XP_016885035, NP_002435 |
| RefSeq mRNA Accession(s) | XM_005262269, XM_017029546, XM_017029545, XM_011530959 NM_002444 |
| RefSeq Genomic Accession(s) | NC_018934, NG_012516, NC_000023 |
| UniProt ID(s) | V9HWC0, P26038 |
| UniGene ID(s) | V9HWC0, P26038 |
| HGNC ID(s) | 7373 |
| Cosmic ID(s) | MSN |
| KEGG Gene ID(s) | hsa:4478 |
| PharmGKB ID(s) | PA31178 |
| General Description of Moesin. | |
| Recognizes 78kDa moesin protein. Moesin, a member of the talin-4.1 superfamily, is a linking protein of the submembraneous actin cytoskeleton. It is expressed in variable amounts in cells of different phenotypes such as macrophages, lymphocytes, fibroblastic, endothelial, epithelial,, neuronal cell lines but not in blood cells. The ERM proteins, ezrin, radixin,, moesin are involved in a variety of cellular functions, such as cell adhesion, migration,, the organization of cell surface structures,, are highly homologous, both in protein sequence, in functional activity, with merlin/schwannomin, a neurofibromatosis-2-associated tumor-suppressor protein. Cell lines of epithelial, mesothelial origin contain both moesin, radixin whereas cells of endothelial, lymphoid origin express moesin. | |
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