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Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) (Apoptosis Marker) Monoclonal Antibody (PRF1/2470)
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Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) (Apoptosis Marker) Monoclonal Antibody (PRF1/2470)

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Perforin-1 단백질을 표적하는 단클론 항체로, 세포사멸(Apoptosis) 마커 연구에 적합. 인간 시료 반응성, IHC 및 Peptide Array에서 사용 가능. Protein A/G 정제, 1 mg/mL 농도, 보존제 무첨가 PBS 용액 형태. -20°C 보관 권장.

카탈로그번호
5551-MSM4-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 07:01
Thermo Fisher Scientific 5551-MSM4-P1ABX Perforin-1 (Pore Forming Protein) (Apoptosis Marker) Monoclonal Antibody (PRF1/2470) 100 ug pk판매 단위 pk ·
재고 확인 필요
900,300원VAT 포함 990,330원

Thermo Fisher Scientific · Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) (Apoptosis Marker) Monoclonal Antibody (PRF1/2470)

Applications and Tested Dilution

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1–2 µg/mL
Peptide Array (Array) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2c, kappa
Class Monoclonal
Type Antibody
Clone PRF1/2470
Immunogen Recombinant human Perforin-1 protein fragment (around aa 413–552)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

Perforin is one of the major cytolytic proteins of cytolytic granules. It acts as a cytolytic mediator stored in and released by cytoplasmic granules and plays a crucial role in immune defense against tumors and viral infections mediated by cytotoxic lymphocytes.
Perforin is a 555 amino acid protein with a 21 amino acid signal peptide and a molecular weight of approximately 70–75 kDa. It forms transmembrane channels similar to complement component C9, sharing structural homology.
Expression of perforin is restricted to killer cell lines and is absent in helper T lymphocytes and other tumor cells. It is a key effector molecule for T-cell and NK-cell-mediated cytolysis. Mutations in the perforin gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder in early childhood. Alternative splicing produces multiple transcript variants.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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