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Thermo Fisher Scientific iNOS Polyclonal Antibody, Biotin
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Thermo Fisher Scientific iNOS Polyclonal Antibody, Biotin

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Human iNOS 단백질을 인식하는 Biotin 결합 Rabbit Polyclonal Antibody. Western blot, ELISA, Immunoprecipitation에 적합. 고순도 Affinity chromatography 정제 제품으로 안정적인 신호 검출 가능. 연구용으로만 사용.

카탈로그번호
INOS-112-BIOTIN
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 05:25
Thermo Fisher Scientific INOS-112-BIOTIN iNOS Polyclonal Antibody, Biotin 200 ul pk판매 단위 pk ·
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594,400원VAT 포함 653,840원

Thermo Fisher Scientific · Thermo Fisher Scientific iNOS Polyclonal Antibody, Biotin

Applications

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
ELISA 1:10,000
Immunoprecipitation (IP) 1:50–1:250

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide within amino acid region 1064–1114 of human inducible nitric oxide synthase (iNOS) protein
Conjugate Biotin
Form Liquid
Concentration 0.5–1.5 mg/mL
Purification Affinity chromatography
Storage Buffer Proprietary buffer (pH 7.4–7.8) with 0.5% BSA, 30% glycerol
Contains 0.02% sodium azide
Storage Conditions −20°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

iNOS (Inducible Nitric Oxide Synthase) is an enzyme responsible for the production of nitric oxide (NO), a gaseous free radical that functions as a signaling molecule in vasorelaxation, neurotransmission, and cytotoxicity.
NO synthesis is mediated by the nitric oxide synthase (NOS) family, which includes three isoforms:

  • nNOS (neuronal, type I)
  • eNOS (endothelial, type III)
  • iNOS (inducible, type II)

iNOS is expressed in various cell types including macrophages, hepatocytes, synoviocytes, and smooth muscle cells. It is inducible by cytokines such as IFN-γ, TNF, IL-1, IL-2, and lipopolysaccharides (LPS). After induction, iNOS shows delayed but sustained activity leading to prolonged NO production.
Dysfunction of iNOS is associated with diseases such as achalasia and impotence.
Three related iNOS pseudogenes are located within the Smith-Magenis syndrome region on chromosome 17.

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

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