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Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) (Apoptosis Marker) Recombinant Rabbit Monoclonal Antibody (PRF1/7077R)
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Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) (Apoptosis Marker) Recombinant Rabbit Monoclonal Antibody (PRF1/7077R)

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Recombinant rabbit monoclonal antibody recognizing human Perforin-1 (PRF1), an apoptosis and cytolytic activity marker. Suitable for IHC applications. Supplied as liquid, unconjugated, 1 mg/mL in PBS. For research use only.

카탈로그번호
5551-RBM6-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 08:07
Thermo Fisher Scientific 5551-RBM6-P1ABX Perforin-1 (Pore Forming Protein) (Apoptosis Marker) Recombinant Rabbit Monoclonal Antibody (PRF1/70 pk판매 단위 pk ·
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904,200원VAT 포함 994,620원

Thermo Fisher Scientific · Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) (Apoptosis Marker) Recombinant Rabbit Monoclonal Antibody (PRF1/7077R)

Applications

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: Assay-dependent

Immunohistochemistry (PFA fixed) (IHC (PFA))

  • Tested Dilution: 1–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG, kappa
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone PRF1/7077R
Immunogen Recombinant human Perforin-1 protein fragment (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 a major cytolytic protein stored in cytoplasmic granules of cytotoxic lymphocytes. It plays a key role in immune defense against tumors and viral infections by forming transmembrane pores in target cells. The protein consists of 555 amino acids, including a 21-amino-acid signal peptide, and has a molecular weight of approximately 70–75 kDa. Perforin shares structural homology with complement component C9 and functions through a similar pore-forming mechanism. It is specifically expressed in killer cell lines, not in helper T lymphocytes or other tumor cells. Mutations in the perforin gene (PRF1) are associated with familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare autosomal recessive immune disorder. Alternative splicing generates multiple transcript variants.


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

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