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Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) Monoclonal Antibody (PRF1, 2467)
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Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) Monoclonal Antibody (PRF1, 2467)

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인간 Perforin-1 단백질을 인식하는 마우스 단클론 항체로, ELISA 및 Peptide Array에 사용 가능. 단백질 A/G로 정제된 액상형 항체이며, 보존제 무첨가 PBS 용액에 1 mg/mL 농도로 제공. 세포독성 림프구 연구 및 면역방어 기전 분석에 적합.

카탈로그번호
5551-MSM1-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 12:19
Thermo Fisher Scientific 5551-MSM1-P1ABX Perforin-1 (Pore Forming Protein) Monoclonal Antibody (PRF1, 2467) 100 ug pk판매 단위 pk ·
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825,100원VAT 포함 907,610원

Thermo Fisher Scientific · Thermo Fisher Scientific Perforin-1 (Pore Forming Protein) Monoclonal Antibody (PRF1, 2467)

Applications

ELISA (ELISA)

  • Tested Dilution: Assay-dependent

Peptide Array (Array)

  • Tested Dilution: Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone PRF1, 2467
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 or -80°C if preferred
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Antibody is tested in direct ELISA.
  • This antibody has only been tested in direct ELISA.

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. Perforin 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 has a molecular weight of approximately 70–75 kDa. It is a pore-forming protein with a mechanism of transmembrane channel formation similar to complement component C9, and homology between perforin and C9 has been demonstrated.

Studies show that perforin is expressed only in killer cell lines, not in helper T lymphocytes or other tumor cells. It is a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis. Mutations in the perforin gene are associated with familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare, lethal 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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