
Thermo Fisher Scientific Perforin Monoclonal Antibody (eBioBOR21), eBioscience
휴먼 퍼포린 단백질을 인식하는 단클론 항체로, 세포독성 T세포 및 NK세포 연구에 적합. Western blot에 1–5 µg/mL로 사용 가능. SDS-PAGE 기준 90% 이상 순도, PBS 완충액(0.09% sodium azide) 보존. 연구용으로만 사용.
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Applications and Tested Dilution
| Application | Tested Dilution | Publications |
|---|---|---|
| Western Blot (WB) | 1–5 µg/mL | View 1 publication |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Published Species | Not Applicable |
| Host / Isotype | Mouse / IgG2b |
| Class | Monoclonal |
| Type | Antibody |
| Clone | eBioBOR21 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.2 |
| Contains | 0.09% sodium azide |
| Storage Conditions | 4°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_468675 |
Product Specific Information
Description:
The eBioBOR21 antibody clone reacts with human perforin (pore-forming protein, pfp). Perforin is a cytolytic mediator present in the cytoplasmic granules of cytotoxic T lymphocytes (CTL) and natural killer (NK) cells. It plays a crucial role in immune defense against tumors and viral infections through target cell lysis.
Applications Tested:
The eBioBOR21 antibody has been tested for use in immunoblotting (WB) of human PBMCs at 1–5 µg/mL. It is recommended to titrate the antibody for optimal performance in specific assays.
Purity: Greater than 90%, as determined by SDS-PAGE.
Aggregation: Less than 10%, as determined by HPLC.
Filtration: 0.2 µm post-manufacturing filtered.
Target Information
Perforin is a major cytolytic protein stored in and released by cytoplasmic granules of cytotoxic lymphocytes. It is a pore-forming protein with a mechanism similar to complement component C9. Perforin consists of 555 amino acids with a 21-amino-acid signal peptide and has a molecular weight of approximately 70–75 kDa. It is specifically expressed in killer cell lines, not in helper T lymphocytes or other tumor cells.
Defects in the perforin gene are associated with familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare autosomal recessive disorder of early childhood. Alternative splicing results in multiple transcript variants of perforin.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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