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ELK Biotechnology IκB-α (phospho Ser32/S36) rabbit pAb
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NF-κB 억제 단백질 IκB-α의 Ser32/Ser36 인산화를 인식하는 토끼 다클론 항체. WB, IHC, IF, ELISA에 적합하며, 사람, 생쥐, 랫드, 원숭이에 반응. 세포 내 NF-κB 신호전달 연구에 유용.
- 카탈로그번호
- ES1345-xxxxx (2개 옵션)
- 판매단위
- pk
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2개 옵션 · 카탈로그 번호를 클릭하면 복사됩니다회원가입 없이 바로 구매하세요
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카탈로그 번호 · 상품 설명출고판매가담기
ELK Biotechnology ES1345-100UL IκB-α (phospho Ser32/S36) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES1345-50UL IκB-α (phospho Ser32/S36) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원
ELK Biotechnology · ELK Biotechnology IκB-α (phospho Ser32/S36) rabbit pAb
제품명
IκB-α (phospho Ser32/S36) rabbit pAb
제품 정보
| 항목 | 내용 |
|---|---|
| Alternative Names | NFKBIA; IKBA; MAD3; NFKBI; NF-kappa-B inhibitor alpha; I-kappa-B-alpha; IkB-alpha; IkappaBalpha; Major histocompatibility complex enhancer-binding protein MAD3 |
| Applications | WB; IHC; IF; ELISA |
| Recommended Dilutions | Western Blot: 1/500–1/2000 Immunohistochemistry: 1/100–1/300 Immunofluorescence: 1/200–1/1000 ELISA: 1/10000 Not yet tested in other applications |
| Immunogen | The antiserum was produced against synthesized peptide derived from human IkappaB-alpha around the phosphorylation site of Ser32/Ser36 (AA range: 15–64) |
| Host Species | Rabbit |
| Storage | -20°C, 1 year |
| Clonality | Polyclonal |
| Isotype | IgG |
| Concentration | 1 mg/ml |
| Observed Band | ~40 kDa |
| Gene ID (Human) | 4792 |
| Human Swiss-Prot No. | P25963 |
| Cellular Localization | Cytoplasm, Nucleus. Shuttles between the nucleus and cytoplasm via NLS and CRM1-dependent nuclear export. |
| Species Reactivity | Human, Mouse, Rat, Monkey |
Background
This gene encodes a member of the NF-kappa-B inhibitor family, which contains multiple ankyrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes involved in inflammatory responses. It shuttles between the cytoplasm and the nucleus through a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene are associated with ectodermal dysplasia anhidrotic with T-cell immunodeficiency (autosomal dominant).
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