
Thermo Fisher Scientific EMAP II Polyclonal Antibody, Biotin, PeproTech
Human EMAP-II 단백질 검출용 Biotin 결합 산양 폴리클로날 항체로, Western blot 및 ELISA에 적합합니다. 고순도 재조합 단백질로 면역화 후 항원 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용 가능합니다.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 0.1–0.2 µg/mL |
| ELISA | 0.25–1.0 µg/mL |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Goat |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | E.coli-derived Recombinant Human EMAP-II |
| Conjugate | Biotin |
| Form | Lyophilized |
| Concentration | 0.1–1.0 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS |
| Contains | No preservative |
| Storage Conditions | -20°C |
| Shipping Conditions | Ambient |
| RRID | AB_2929627 |
Product Specific Information
- Preparation: Produced from sera of goats immunized with highly pure Recombinant Human EMAP-II. Anti-Human EMAP-II-specific antibody was purified by affinity chromatography and then biotinylated.
- Sandwich ELISA: For detection of hEMAP-II using 100 µL/well, use 0.25–1.0 µg/mL of this antibody. In conjunction with PeproTech Polyclonal Anti-Human EMAP-II (500-P172G) as capture antibody, enables detection of at least 0.2–0.4 ng/well of Recombinant hEMAP-II.
- Western Blot: For detection of hEMAP-II, use 0.1–0.2 µg/mL. Detection limit for Recombinant hEMAP-II is 1.5–3.0 ng/lane under reducing or non-reducing conditions.
- Packaging: 500-P172GBT-1MG will be provided as 2 × 500 µg.
Target Information
The protein encoded by this gene is a cytokine specifically induced by apoptosis, involved in the regulation of angiogenesis, inflammation, and wound healing. Its release sensitizes tumor-associated vasculature to tumor necrosis factor. The precursor protein is identical to the p43 subunit of the multi-tRNA synthetase complex and modulates aminoacylation activity in normal cells. It also stimulates inflammatory responses after proteolytic cleavage in tumor cells. Multiple transcript variants exist, and a pseudogene has been identified on chromosome 20.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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