
ELK Biotechnology WASP rabbit pAb
WASP rabbit pAb는 인간 및 마우스 시료에 반응하는 폴리클로날 항체로, WB, IHC, IF, ELISA에 적합합니다. 인간 WASP 유래 펩타이드로 면역화되었으며, 세포질 및 핵에 위치한 단백질 검출에 유용합니다. -20°C에서 1년 보관 가능합니다.
- 판매단위
- pk
카탈로그
2개 옵션 · 카탈로그 번호를 클릭하면 복사됩니다ELK Biotechnology · ELK Biotechnology WASP rabbit pAb
제품명
WASP rabbit pAb
제품 정보
| 항목 | 내용 |
|---|---|
| Alternative Names | WAS; IMD2; Wiskott-Aldrich syndrome protein; WASp |
| Applications | WB; IHC; IF; ELISA |
| Recommended Dilutions | Western Blot: 1/500 - 1/2000 Immunohistochemistry: 1/100 - 1/300 ELISA: 1/5000 Not yet tested in other applications |
| Immunogen | Synthesized peptide derived from human WASP (AA range: 256–305) |
| Host | Rabbit |
| Storage | -20°C / 1 year |
| Clonality | Polyclonal |
| Isotype | IgG |
| Concentration | 1 mg/ml |
| Observed Band | 60 kD |
| Gene ID (Human) | 7454 |
| Human Swiss-Prot No. | P42768 |
| Cellular Localization | Cytoplasm, cytoskeleton, nucleus |
| Species Reactivity | Human, Mouse |
Background
The Wiskott-Aldrich syndrome (WAS) family of proteins share similar domain structures and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton. These proteins are regulated by multiple stimuli and interact with various proteins. Studies have shown that they associate with the small GTPase Cdc42, which regulates actin filament formation, and the cytoskeletal organizing complex Arp2/3.
Wiskott-Aldrich syndrome is a rare, inherited, X-linked recessive disease characterized by immune dysregulation and microthrombocytopenia, caused by mutations in the WAS gene. The WAS gene product is a cytoplasmic protein expressed exclusively in hematopoietic cells, showing signaling and cytoskeletal abnormalities in WAS patients.
ELK Biotechnology 상품 둘러보기
전체보기문의
0개 · 배송·재고 문의는 실시간 상담이 빠릅니다아직 등록된 문의가 없어요.
