Gelsolin 抗体
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- 抗原 See all Gelsolin (GSN) 抗体
- Gelsolin (GSN)
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This Gelsolin antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Purified by Protein A/G
- 免疫原
- Recombinant human full-length protein
- 克隆位点
- CPTC-Gelsolin-1
- 亚型
- IgG1 kappa
- Top Product
- Discover our top product GSN Primary Antibody
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- 应用备注
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Positive Control: MCF cell lysate, Tonsil.
Known Application: Western Blot (0.5-1.0 μg/mL), Optimal dilution for a specific application should be determined.
- 限制
- 仅限研究用
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- 浓度
- 200 μg/mL
- 缓冲液
- 10 mM PBS with 0.05 % BSA & 0.05 % azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-80 °C
- 储存方法
- Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required.
- 有效期
- 24 months
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- 抗原
- Gelsolin (GSN)
- 别名
- GSN (GSN 产品)
- 别名
- ADF antibody, AGEL antibody, CG1106 antibody, DGS antibody, Dmel\\CG1106 antibody, gel antibody, scin antibody, cb107 antibody, gsn antibody, sb:cb107 antibody, u-gelsolin antibody, wu:fi16f06 antibody, gelsolin antibody, Gelsolin antibody, gelsolin S homeolog antibody, gelsolin a antibody, GSN antibody, Gel antibody, Gsn antibody, gsn.S antibody, gsn antibody, gsna antibody
- 背景
- Gelsolin (also known as brevin, Actin-depolymerizing factor or ADF), a proteinof leukocytes, platelets and other cells, severs Actin filaments in thepresence of submicromolar calcium, thereby isolating cytoplasmic Actin gels. It is a calcium-regulated, actin-modulating protein that binds to the plus (or barbed) ends of actin monomers or filaments, preventing monomer exchange (end-blocking or capping). It can promote the assembly of monomers into filaments (nucleation) as well as sever filaments already formed. Plays a role in ciliogenesis. Defects in GSN are the cause of amyloidosis type 5 (AMYL5), also known as familial amyloidosis Finnish type, typically characterized by cranial neuropathy and lattice corneal dystrophy. Severe systemic disease can develop in some individuals causing peripheral polyneuropathy, amyloid cardiomyopathy, and nephrotic syndrome leading to renal failure.
- 分子量
- 90kDa
- 基因ID
- 2934
- UniProt
- P06396
- 途径
- Caspase Cascade in Apoptosis, Regulation of Actin Filament Polymerization, Autophagy
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