Advillin 抗体 (AA 151-250) (Biotin)
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- 抗原 See all Advillin (AVIL) 抗体
- Advillin (AVIL)
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抗原表位
- AA 151-250
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适用
- 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This Advillin antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Cow,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Advillin
- 亚型
- IgG
- Top Product
- Discover our top product AVIL Primary Antibody
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- Advillin (AVIL)
- 别名
- Advillin (AVIL 产品)
- 别名
- Adv antibody, SpAdv antibody, villin antibody, zgc:136857 antibody, ADVIL antibody, DOC6 antibody, p92 antibody, Advil antibody, advillin antibody, AVIL antibody, adv antibody, avil antibody, CpipJ_CPIJ004696 antibody, Avil antibody
- 背景
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Synonyms: Actin binding protein DOC 6, Actin binding protein DOC6, Advil, Advillin, AVIL, AVIL_HUMAN, DOC 6, DOC6, p92.
Background: Advillin is an 819 amino acid protein that localizes to both the cytoplasm and the cytoskeleton and contains one HP domain and six gelsolin-like repeats. Expressed at high levels in colon and small intestine and at lower levels in uterus, thymus, testis and prostate, advillin functions as a calcium-regulated Actin-binding protein that may be involved in the development of neuronal cells, specifically those that form ganglia. The gene encoding advillin maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
- 基因ID
- 3316
- 途径
- Regulation of Actin Filament Polymerization
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