CCDC19 抗体 (Cy5)
Quick Overview for CCDC19 抗体 (Cy5) (ABIN719145)
抗原
See all CCDC19 抗体适用
宿主
克隆类型
标记
应用范围
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预测反应
- Human,Mouse,Rat,Cow,Sheep,Horse,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human CCDC19
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亚型
- IgG
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anti-Coiled-Coil Domain Containing 19 (CCDC19) antibody
CCDC19 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 19 (CCDC19) (N-Term) antibodyCCDC19 适用: 人, 犬, 马, Cow, 豚鼠, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 19 (CCDC19) (N-Term) antibodyCCDC19 适用: 人, 犬, 马, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 19 (CCDC19) (AA 106-135), (N-Term) antibodyCCDC19 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB30101 unconjugated
anti-Coiled-Coil Domain Containing 19 (CCDC19) (AA 113-143), (N-Term) antibodyCCDC19 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
- IF(IHC-P) 1:50-200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))
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别名
- Ccdc19
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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.
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基因ID
- 25790
抗原
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