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Thermo Fisher Scientific Perforin Monoclonal Antibody (dG9)
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Thermo Fisher Scientific Perforin Monoclonal Antibody (dG9)

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Human Perforin 단백질을 인식하는 Mouse IgG2b 단일클론 항체. Western blot 및 파라핀 포매 조직면역염색에 적합. Protein A 정제, 액상 형태로 제공되며 안정화제가 포함된 PBS 버퍼에 보관. 세포막 및 분비 위치의 perforin 검출에 유용.

카탈로그번호
604-820
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 08:39
Thermo Fisher Scientific 604-820 Perforin Monoclonal Antibody (dG9) 100 ug pk판매 단위 pk ·
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421,400원VAT 포함 463,540원

Thermo Fisher Scientific · Thermo Fisher Scientific Perforin Monoclonal Antibody (dG9)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 0.1–1 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 2–10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone dG9
Immunogen Recombinant protein of human Perforin
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Protein A
Storage Buffer PBS with proprietary stabilizer
Contains 0.01% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Positive control: Spleen
  • Cellular location: Secreted, Cell membrane

Target Information

Perforin is a major cytolytic protein found in cytolytic granules. It acts as a cytolytic mediator released by cytotoxic lymphocytes to defend against tumors and viral infections. The protein consists of 555 amino acids, including a 21 amino acid signal peptide, with a molecular weight of approximately 70–75 kDa. Perforin functions as a pore-forming protein, similar in mechanism to complement component C9, with demonstrated homology between the two.

Perforin expression is restricted to killer cell lines and absent in helper T lymphocytes or other tumor cells. It is a key effector molecule in T-cell and natural killer (NK) cell-mediated cytolysis. Mutations in the perforin gene are associated with familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and 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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