CCDC11 抗体 (AA 330-380) (AbBy Fluor® 594)
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- 抗原 See all CCDC11 抗体
- CCDC11 (Coiled-Coil Domain Containing 11 (CCDC11))
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抗原表位
- AA 330-380
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适用
- 人, 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 CCDC11 antibody is conjugated to AbBy Fluor® 594
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 特异性
- Due to the similarity of this protein to RWD domain-containing protein 1, there is a chance that this antibody will react with this protein based on a 75 % non-sequential amino acid similarity.
- 交叉反应
- 人, 小鼠, 大鼠
- 预测反应
- Cow,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CCDC11
- 亚型
- IgG
- Top Product
- Discover our top product CCDC11 Primary Antibody
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- 应用备注
- IF(IHC-P) 1:50-200
- 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
- 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
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- CCDC11 (Coiled-Coil Domain Containing 11 (CCDC11))
- 别名
- CCDC11 (CCDC11 产品)
- 别名
- 4933415I03Rik antibody, HTX6 antibody, RGD1306734 antibody, CCDC11 antibody, ccdc11 antibody, si:ch211-257i19.2 antibody, zgc:153145 antibody, cilia and flagella associated protein 53 antibody, Cfap53 antibody, CFAP53 antibody, cfap53 antibody
- 背景
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Synonyms: HTX6, CCDC11, Coiled-coil domain-containing protein 11
Background: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
- 基因ID
- 220136
- UniProt
- Q96M91
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