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Rabbit Polyclonal MYLK Antibody

  • 中文名: MYLK抗体
  • 别    名: KRP; AAT7; MLCK; MLCK1; MYLK1; smMLCK; MLCK108; MLCK210; MSTP083
货号: IPDX12577
Price: ¥1180
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 1/25-1/100 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 1/5000-1/10000 Human,Mouse,Rat

产品详情

AliasesKRP; AAT7; MLCK; MLCK1; MYLK1; smMLCK; MLCK108; MLCK210; MSTP083
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
ImmunogenSynthetic peptide of human MYLK
FormulationPurified antibody in PBS with 0.05% sodium azide and 50% glycerol.

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参考文献

以下是3篇关于MYLK抗体的代表性文献及其摘要概括:

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1. **文献名称**:*"Myosin light chain kinase regulates endothelial cell barrier function"*

**作者**:Garcia, J.G.N. 等(2001)

**摘要**:研究利用MYLK抗体验证了肌球蛋白轻链激酶(MYLK)在内皮细胞屏障功能中的作用,发现抑制MYLK活性可减少炎症相关血管通透性增加。

2. **文献名称**:*"Tumor cell cytoskeleton reorganization by MYLK-mediated contractility drives cancer cell invasion"*

**作者**:Dudek, S.M. 等(2013)

**摘要**:通过MYLK抗体检测发现,肿瘤细胞中MYLK通过磷酸化肌球蛋白轻链(MLC)促进细胞骨架收缩,从而增强癌细胞迁移和侵袭能力。

3. **文献名称**:*"Smooth muscle myosin light chain kinase knockout mice reveal pleiotropic effects in vascular development"*

**作者**:He, W.Q. 等(2013)

**摘要**:利用基因敲除模型和MYLK抗体实验,揭示MYLK缺失导致平滑肌收缩功能异常,进而影响血管发育和血压调控。

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这些研究均通过MYLK抗体明确蛋白表达或功能,涵盖血管疾病、肿瘤转移和发育生物学领域,可作为MYLK相关机制研究的参考。

背景信息

Myosin light chain kinase (MYLK) is a calcium/calmodulin-dependent enzyme that plays a critical role in regulating smooth muscle and non-muscle cell contraction. It phosphorylates the regulatory light chains of myosin, activating actin-myosin interactions, which drive cellular processes like motility, migration, and vascular tone. MYLK exists in multiple isoforms, including long (smooth muscle) and short (non-muscle) forms, with distinct tissue distributions and functions. MYLK antibodies are essential tools for studying its expression, localization, and activity in physiological and pathological contexts. Research has linked MYLK dysregulation to cardiovascular diseases (e.g., hypertension, aneurysms), inflammatory conditions, and cancer metastasis, where aberrant cell contractility or endothelial barrier disruption occurs. MYLK mutations are also implicated in hereditary aortic disorders, such as familial thoracic aortic aneurysms and dissections (TAAD). Antibodies targeting specific MYLK isoforms enable investigations into its tissue-specific roles, post-translational modifications, and interactions with signaling pathways. They are widely used in techniques like Western blotting, immunohistochemistry, and functional assays to explore MYLK's contribution to disease mechanisms or therapeutic targeting. Validation of MYLK antibodies remains crucial due to isoform complexity and cross-reactivity risks.

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