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Rabbit Monoclonal FLAP Antibody

  • 中文名: FLAP抗体
  • 别    名: ALOX 5AP; ALOX5 AP; ALOX5AP; FLAP;;FLAP
货号: IPDX18413
Price: ¥1280
数量:
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验证与应用

应用及物种
WB 1/1000-1/2000 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 咨询技术 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesALOX 5AP; ALOX5 AP; ALOX5AP; FLAP;;FLAP
WB Predicted band sizeCalculated MW: 18 kDa ; Observed MW: 16 kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman
ImmunogenA synthesized peptide derived from human FLAP
FormulationPurified antibody in PBS with 0.05% sodium azide,0.05% BSA and 50% glycerol.

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参考文献

以下是关于FLAP(5-脂氧合酶激活蛋白)抗体的3篇代表性文献摘要概括:

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1. **文献名称**:*Cloning of the cDNA for human 5-lipoxygenase-activating protein (FLAP)*

**作者**:Dixon, R.A. et al.

**摘要**:该研究首次克隆并鉴定了人类FLAP基因,揭示了其作为5-脂氧合酶(5-LO)关键辅助蛋白的功能,证明FLAP是白三烯生物合成的必要调节因子,为后续炎症和哮喘相关药物靶点研究奠定基础。

2. **文献名称**:*Pharmacological characterization of a novel FLAP inhibitor, MK-591*

**作者**:Evans, J.F. et al.

**摘要**:报道了FLAP抑制剂MK-591的开发,通过抑制FLAP与5-LO的相互作用阻断白三烯生成,在动物模型中显著减轻炎症反应,并进入早期临床试验用于哮喘和动脉粥样硬化治疗。

3. **文献名称**:*Association of FLAP gene polymorphisms with myocardial infarction*

**作者**:Helgadottir, A. et al.

**摘要**:通过全基因组关联分析,发现FLAP基因(ALOX5AP)特定单核苷酸多态性(SNPs)与心肌梗死风险显著相关,提示FLAP在心血管疾病炎症通路中的潜在作用。

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以上文献涵盖FLAP的分子机制、抑制剂开发及疾病关联研究,可供快速参考。如需具体期刊信息或扩展,可进一步检索PubMed或SciFinder数据库。

背景信息

The 5-lipoxygenase-activating protein (FLAP), encoded by the *ALOX5AP* gene, is a critical mediator in the leukotriene biosynthesis pathway. Discovered in the 1990s, FLAP facilitates the interaction between 5-lipoxygenase (5-LO) and arachidonic acid, a key step in producing pro-inflammatory leukotrienes (LTs) like LTB4 and cysteinyl-LTs. These lipid mediators drive inflammatory responses in diseases such as asthma, atherosclerosis, and rheumatoid arthritis. FLAP’s role involves anchoring 5-LO to the nuclear membrane, enabling substrate transfer and enzyme activation. Genetic studies link *ALOX5AP* polymorphisms to increased cardiovascular and inflammatory disease risks, highlighting its therapeutic relevance. FLAP inhibitors, like MK-886. were developed to block LT synthesis, showing efficacy in preclinical models. However, clinical translation faced challenges due to off-target effects. FLAP-specific antibodies remain vital tools for studying protein localization, expression levels, and mechanistic interactions in cellular and tissue models. Recent research explores FLAP's involvement in viral infections (e.g., COVID-19) and cancer, broadening its pathophysiological significance. Despite setbacks in drug development, FLAP remains a promising target for modulating inflammation, with ongoing studies aiming to refine inhibitors and biologics for precision therapies.

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