
ELK Biotechnology Tie2 (phospho-Ser1119) rabbit pAb
Tie2 (phospho-Ser1119) rabbit pAb는 인체, 생쥐, 랫드에서 반응하는 인산화형 Tie2 단백질 검출용 항체입니다. WB와 IHC에 적합하며, 세포막 및 세포골격 위치 연구에 활용됩니다. 고순도 폴리클로날 IgG로 안정적 장기 보관이 가능합니다.
- 판매단위
- pk
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제품명
Tie2 (phospho-Ser1119) rabbit pAb
주요 정보
| 항목 | 내용 |
|---|---|
| Alternative Names | Angiopoietin-1 receptor (EC 2.7.10.1), Endothelial tyrosine kinase, Tunica interna endothelial cell kinase, Tyrosine kinase with Ig and EGF homology domains-2, Tyrosine-protein kinase receptor TEK, Tyrosine-protein kinase receptor TIE-2, hTIE2, p140 TEK, CD antigen CD202b |
| Applications | WB; IHC |
| Recommended Dilutions | WB 1:500–2000; IHC-p 1:50–300 |
| Immunogen | Synthesized phospho peptide around human Tie2 (Ser1119) |
| Host | Rabbit |
| Storage | -20°C / 1 year |
| Clonality | Polyclonal |
| Isotype | IgG |
| Concentration | 1 mg/ml |
| Observed Band | 120 kD |
| GeneID (Human) | 7010 |
| Human Swiss-Prot No | Q02763 |
| Species Reactivity | Human; Rat; Mouse |
세포 내 위치
Cell membrane; Single-pass type I membrane protein.
Cell junction, focal adhesion, cytoplasm, cytoskeleton, secreted.
Recruited to cell-cell contacts in quiescent endothelial cells (PubMed:18425120, PubMed:18425119).
Colocalizes with actin cytoskeleton and stress fibers during cell spreading.
Recruited to the lower surface of migrating cells, especially the rear end.
Proteolytic processing gives rise to a soluble extracellular domain that is secreted (PubMed:11806244).
배경 설명
This gene encodes a receptor belonging to the protein tyrosine kinase Tie2 family. The encoded protein has a unique extracellular region containing two immunoglobulin-like domains, three epidermal growth factor (EGF)-like domains, and three fibronectin type III repeats. The ligand angiopoietin-1 binds to this receptor, mediating a signaling pathway involved in embryonic vascular development. Mutations in this gene are associated with inherited venous malformations of the skin and mucous membranes. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants have been described, but their full-length nature is not known. [RefSeq, Feb 2014]
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