CCDC19 抗体 (Cy5)
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- 抗原 See all CCDC19 抗体
- CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))
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适用
- 人, 大鼠, 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 CCDC19 antibody is conjugated to Cy5
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应用范围
- Western Blotting (WB)
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CCDC19
- 亚型
- IgG
- Top Product
- Discover our top product CCDC19 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
- CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))
- 别名
- Ccdc19 (CCDC19 产品)
- 别名
- nesg1 antibody, MGC76242 antibody, CCDC19 antibody, NESG1 antibody, 1700028D05Rik antibody, Nesg1 antibody, cilia and flagella associated protein 45 antibody, cilia and flagella associated protein 45 S homeolog antibody, coiled-coil domain-containing protein 19, mitochondrial antibody, cfap45 antibody, CFAP45 antibody, cfap45.S antibody, LOC748703 antibody, Cfap45 antibody
- 背景
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Synonyms: Coiled coil domain containing 19, Nasopharyngeal epithelium specic protein 1, NESG1, RP11 190A12.6, CCD19_HUMAN.
Background: CCDC19 is a 466 amino acid protein encoded by a gene mapping to human chromosome 1. Chromosome 1 is the largest human chromosome, spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1 and, considering the great number of genes, there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes Lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinson?s, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
- 基因ID
- 25790
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