
Thermo Fisher Scientific Phospho-MYH9 (Ser1803) Polyclonal Antibody
Phospho-MYH9 (Ser1803) 폴리클로날 항체로, 인간·마우스·랫트 시료에서 Myosin IIA 인산화 형태를 검출. Western blot에 적합하며, 항원 친화 크로마토그래피로 정제됨. 세포 이동 및 형태 유지 연구에 활용 가능.
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Applications
Western Blot (WB)
- Tested Dilution: 1:1,000
- Publications: [References not provided]
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Phospho-Myosin IIA Heavy Chain (Ser1803) synthetic peptide (coupled to KLH) corresponding to amino acid residues surrounding Ser1803 in human myosin IIA heavy chain. This sequence is highly conserved in rat and mouse myosin IIA heavy chain and shows some homology to conserved sites in non-muscle myosin IIB and smooth muscle myosin heavy chains. |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage buffer | PBS with 1 mg/mL BSA, 50% glycerol |
| Contains | 0.05% sodium azide |
| Storage conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping conditions | Wet ice |
| RRID | AB_2942946 |
Product Specific Information
This antibody was cross-adsorbed to unphosphorylated Myosin IIA Heavy Chain (Ser-1803) peptide before affinity purification using phospho-Myosin IIA Heavy Chain (Ser-1803) peptide (without carrier).
The antibody detects a 200 kDa* protein corresponding to Myosin IIA Heavy Chain on SDS-PAGE immunoblots of human A431 cells treated with Calyculin A.
This reactivity is removed after treatment with lambda phosphatase.
Target Information
The MYH9 gene, located on chromosome 22q12.3, encodes the heavy chain of non-muscle myosin IIA (NMHC IIA), a critical component of the actin cytoskeleton that plays essential roles in various cellular processes.
- The MYH9 gene spans over 106 kilobases and includes 41 exons encoding a 1,960-amino-acid protein.
- NMHC IIA forms a hexameric complex with two heavy chains, two regulatory light chains, and two essential light chains.
- It interacts with actin filaments, contributing to cell migration, adhesion, division, and shape maintenance.
- Mutations in MYH9 cause autosomal dominant MYH9-related diseases (MYH9-RD) such as May-Hegglin anomaly, Fechtner syndrome, and Epstein syndrome.
- These disorders are associated with macrothrombocytopenia and may lead to hearing loss, renal failure, and cataracts.
- MYH9 is essential for hematopoiesis, maintaining hematopoietic stem and progenitor cells (HSPCs). Loss of function can result in severe blood cell deficiencies and bone marrow failure.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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