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Rabbit Monoclonal SPINK5/LEKTI Antibody

  • 中文名: SPINK5/LEKTI抗体
  • 别    名: LEKTI; NETS; SPINK5; VAKTI;;SPINK5
货号: IPDX19063
Price: ¥1280
数量:
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验证与应用

应用及物种
WB 咨询技术 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

AliasesLEKTI; NETS; SPINK5; VAKTI;;SPINK5
WB Predicted band size121 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,Mouse,Rat
ImmunogenA synthesized peptide derived from human SPINK5
FormulationPurified antibody in PBS with 0.05% sodium azide,0.05% BSA and 50% glycerol.

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参考文献

1. **《SPINK5 and Netherton syndrome: Novel mutations and immunological findings》**

- 作者:Descargues P et al.

- 摘要:研究报道了Netherton综合征患者中SPINK5基因的新突变,并通过LEKTI抗体检测皮肤组织中LEKTI蛋白的异常表达,揭示了其与皮肤屏障缺陷和炎症反应的关系。

2. **《LEKTI proteolytic processing in human primary keratinocytes, tissue distribution, and defective expression in Netherton syndrome》**

- 作者:Bitoun E et al.

- 摘要:利用特异性LEKTI抗体分析人皮肤角质细胞中LEKTI蛋白的分段加工过程,发现Netherton综合征患者中LEKTI表达缺失,导致丝氨酸蛋白酶活性失调。

3. **《Antibodies targeting the C-terminal domain of LEKTI restore stratum corneum integrity in Netherton syndrome》****

- 作者:Furio L et al.

- 摘要:开发针对LEKTI蛋白C端结构域的单克隆抗体,通过体外皮肤模型验证其修复Netherton综合征患者角质层屏障的功能,为治疗提供潜在策略。

4. **《Immunohistochemical analysis of LEKTI expression in normal and pathological skin》**

- 作者:Komatsu N et al.

- 摘要:采用免疫组化技术结合LEKTI抗体,系统比较正常皮肤与Netherton综合征等疾病皮肤中LEKTI的分布差异,揭示其在表皮分化中的调控作用。

背景信息

SPINK5 (Serine Peptidase Inhibitor Kazal-Type 5) encodes LEKTI (Lympho-Epithelial Kazal-Type-Related Inhibitor), a multidomain serine protease inhibitor critical for skin barrier integrity and immune regulation. Expressed in stratified epithelia (e.g., skin, thymus), LEKTI modulates proteolytic cascades by inhibiting kallikreins and other proteases that regulate desquamation, inflammation, and antimicrobial defense. Mutations in SPINK5 cause Netherton syndrome, a severe autosomal recessive disorder characterized by congenital ichthyosiform erythroderma, hair shaft defects, and atopic manifestations due to uncontrolled protease activity and epidermal disruption.

LEKTI antibodies are tools used in research and diagnostics to detect protein expression, localization, or deficiency in tissues. In Netherton syndrome, reduced/absent LEKTI detected via immunohistochemistry aids diagnosis. Research applications include studying LEKTI's role in skin homeostasis, inflammatory pathways (e.g., PAR-2 signaling), and therapeutic strategies (e.g., protease inhibitors or gene therapy). Commercial antibodies target specific LEKTI domains (e.g., D9. D15) to assess functional fragments. Challenges include cross-reactivity due to LEKTI's complex 15-domain structure and post-translational processing. Recent studies also explore LEKTI's potential as a biomarker in atopic dermatitis and cancer.

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