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Thermo Fisher Scientific Perforin Polyclonal Antibody
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Thermo Fisher Scientific Perforin Polyclonal Antibody

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Perforin 단백질을 검출하는 Thermo Fisher Scientific의 폴리클로날 항체로, WB 및 IHC(P) 실험에 적합. 사람, 마우스, 랫트 반응성. Rabbit IgG로 제작, 액상 형태, 1 mg/mL 농도. 면역세포 관련 연구 및 세포독성 단백질 분석에 활용 가능.

카탈로그번호
PA5102303
판매단위
pk
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마지막 업데이트 2025. 07. 31. 오전 08:29
Thermo Fisher Scientific PA5102303 Perforin Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific Perforin Polyclonal Antibody

Thermo Fisher Scientific Perforin Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human PRF1 (Accession P14222), corresponding to amino acid residues T74–S124
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2851712

Product Specific Information

Antibody detects endogenous levels of total PRF1.

Target Information

Perforin is one of the major cytolytic proteins of cytolytic granules. It acts as a cytolytic mediator stored and released by cytoplasmic granules and is involved 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 70–75 kDa. It forms transmembrane channels similar to complement component C9, showing structural homology.
Expression of perforin is restricted to killer cell lines and absent in helper T lymphocytes or other tumor cells. It is a key effector molecule for T-cell and natural killer cell-mediated cytolysis.
Defects in the perforin gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder of early childhood. Alternative splicing results in multiple transcript variants.

Usage Note

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

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