C1orf163 抗体
-
- 抗原 See all C1orf163 抗体
- C1orf163 (Chromosome 1 Open Reading Frame 163 (C1orf163))
-
适用
- 人, 小鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C1orf163 antibody is un-conjugated
-
应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Full length fusion protein
- 亚型
- IgG
-
anti-Chromosome 1 Open Reading Frame 163 (C1orf163) (AA 1-231) antibody
C1orf163 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1G11-1C4 unconjugated
anti-Chromosome 1 Open Reading Frame 163 (C1orf163) antibodyC1orf163 适用: 人, 大鼠, 小鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
- WB 1:500-1:2000, IHC 1:40-1:200, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 0.9 mg/mL
- 缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 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. Avoid freeze / thaw cycles.
-
- 抗原
- C1orf163 (Chromosome 1 Open Reading Frame 163 (C1orf163))
- 别名
- COA7 (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
- The cytochrome c oxidase (COX) family of proteins function as the final electron donor in the respiratory chain to drive a proton gradient across the inner mitochondrial membrane, ultimately resulting in the production of water. COA7 (cytochrome c oxidase assembly factor 7), also known as RESA1, SELRC1 or C1orf163, is a 231 amino acid mitochondrial protein that belongs to the hcp beta-lactamase family. Consisting of five Sel1-like repeats, COA7 may be associated with respiratory chain assembly. COA7 is encoded by a gene located on human chromosome 1p32.3. 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.
- 分子量
-
Observed_MW: Refer to figures
Calculated_MW: 26 kDa
- UniProt
- Q96BR5
-
