C1orf163 抗体
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- 抗原 See all C1orf163 抗体
- C1orf163 (Chromosome 1 Open Reading Frame 163 (C1orf163))
- 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 C1orf163 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C1orf163
- 亚型
- IgG
- Top Product
- Discover our top product C1orf163 Primary Antibody
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anti-Chromosome 1 Open Reading Frame 163 (C1orf163) antibody
C1orf163 适用: 人, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 1 Open Reading Frame 163 (C1orf163) (AA 1-231) antibodyC1orf163 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1G11-1C4 unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- C1orf163 (Chromosome 1 Open Reading Frame 163 (C1orf163))
- 别名
- C1orf163 (C1orf163 产品)
- 别名
- C1orf163 antibody, 2010305A19Rik antibody, AI451324 antibody, D4Ertd796e antibody, cytochrome c oxidase assembly factor 7 (putative) antibody, cytochrome c oxidase assembly factor 7 antibody, COA7 antibody, Coa7 antibody
- 背景
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Synonyms: Chromosome 1 open reading frame 163, FLJ12439, Hcp beta lactamase like protein C1orf163, Hypothetical protein LOC65260,SELR1_HUMAN.
Background: 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, Parkinsons, 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. The C1orf163 gene product has been provisionally designated C1orf163 pending further characterization.
- 基因ID
- 65260
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