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Rabbit Polyclonal BLOC1S6 Antibody

  • 中文名: BLOC1S6抗体
  • 别    名: PA; HPS9; PLDN; BLOS6; PALLID
货号: IPDX10266
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 1/100-1/300 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

AliasesPA; HPS9; PLDN; BLOS6; PALLID
WB Predicted band size20 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
ImmunogenFusion protein of human BLOC1S6
FormulationPurified antibody in PBS with 0.05% sodium azide and 50% glycerol.

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参考文献

以下是关于BLOC1S6抗体的3篇参考文献(基于模拟生成,实际文献可能需要通过学术数据库检索确认):

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1. **标题**: "BLOC1S6 regulates lysosomal trafficking in melanocytes via interactions with the kinesin motor protein"

**作者**: Smith A, et al.

**摘要**: 本研究利用BLOC1S6特异性抗体,揭示了该蛋白在黑素细胞中通过驱动蛋白(kinesin)介导的溶酶体运输机制,并发现其缺陷与色素沉着异常相关。

2. **标题**: "Dysregulation of BLOC1S6 in Hermansky-Pudlak syndrome type 9: antibody validation and functional analysis"

**作者**: Chen L, et al.

**摘要**: 研究通过Western blot和免疫荧光验证了BLOC1S6抗体的特异性,发现BLOC1S6基因突变导致溶酶体相关细胞器(LRO)生成异常,与赫曼斯基-普德拉克综合征9型相关。

3. **标题**: "BLOC1S6 interacts with AP-3 complex to mediate cargo sorting in neuronal cells"

**作者**: Gomez TS, et al.

**摘要**: 结合BLOC1S6抗体的共聚焦成像技术,研究发现该蛋白在神经元中与AP-3复合体协作,调控突触小泡的蛋白质分选过程,影响神经信号传递。

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如需具体文献,建议通过PubMed或Google Scholar检索关键词“BLOC1S6 antibody”或“BLOC1S6 function”获取最新研究。

背景信息

The BLOC1S6 antibody targets the BLOC1S6 protein, a subunit of the Biogenesis of Lysosome-related Organelles Complex 1 (BLOC-1). This multisubunit protein complex is critical for the formation and trafficking of lysosome-related organelles (LROs), such as melanosomes, platelet dense granules, and synaptic vesicles. BLOC1S6. also known as Pallidin, plays a role in membrane protein sorting and vesicle biogenesis, particularly in specialized cell types like melanocytes and neurons. Mutations in BLOC1S6 are linked to Hermansky-Pudlak syndrome (HPS), a rare genetic disorder characterized by oculocutaneous albinism, bleeding diathesis, and lysosomal dysfunction. Antibodies against BLOC1S6 are essential tools for studying the molecular mechanisms underlying LRO biogenesis, protein trafficking pathways, and HPS pathogenesis. They enable detection of BLOC1S6 expression via techniques like Western blotting, immunohistochemistry, and immunofluorescence, aiding in the identification of protein localization and interactions within the BLOC-1 complex. Research using these antibodies has contributed to understanding how BLOC-1 dysfunction disrupts cellular processes, offering insights into therapeutic strategies for HPS and related lysosomal disorders. Commercial BLOC1S6 antibodies are typically validated for specificity and sensitivity, ensuring reliability in both diagnostic and experimental contexts.

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