COX4NB 抗体
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- 抗原 See all COX4NB 抗体
- COX4NB (COX4 Neighbor (COX4NB))
- 适用
- 人, 小鼠, 大鼠
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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 COX4NB antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human EMC8
- 亚型
- IgG
- Top Product
- Discover our top product COX4NB Primary Antibody
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anti-COX4 Neighbor (COX4NB) (AA 1-210) antibody
COX4NB 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-COX4 Neighbor (COX4NB) (AA 1-210) antibodyCOX4NB 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-COX4 Neighbor (COX4NB) (AA 113-210) antibodyCOX4NB 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4F4 unconjugated
anti-COX4 Neighbor (COX4NB) antibodyCOX4NB 适用: 人 WB, DB, ICC 宿主: 小鼠 Monoclonal 2643C6a unconjugated
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- 应用备注
- WB 1:500-1:2000, IHC 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.4 mg/mL
- 缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 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.
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- 抗原
- COX4NB (COX4 Neighbor (COX4NB))
- 别名
- EMC8 (COX4NB 产品)
- 别名
- COX4NB antibody, NOC4 antibody, MGC75783 antibody, cox4nb antibody, fb54g02 antibody, noc4 antibody, wu:fb54g02 antibody, zgc:56331 antibody, C16orf2 antibody, C16orf4 antibody, FAM158B antibody, Cox4nb antibody, Fam158b antibody, Noc4 antibody, ER membrane protein complex subunit 8 antibody, ER membrane protein complex subunit 8 S homeolog antibody, ER membrane protein complex subunit 9 antibody, EMC8 antibody, emc8 antibody, emc8.S antibody, EMC9 antibody, Emc8 antibody
- 背景
- COX4NB (Neighbor of COX4) is a 210 amino acid protein encoded by the human gene COX4NB. COX4NB belongs to the UPF0172 (NOC4) family and is found on chromosome 16, adjacent to the gene that encodes COX4. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other auto-immune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
- 分子量
- 24 kDa
- UniProt
- O43402
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