COX4NB 抗体 (AA 121-210)
Quick Overview for COX4NB 抗体 (AA 121-210) (ABIN1387995)
抗原
See all COX4NB 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 121-210
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预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,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 COX4NB
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亚型
- IgG
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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 113-210) antibodyCOX4NB 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4F4 unconjugated
anti-COX4 Neighbor (COX4NB) (AA 1-210) antibodyCOX4NB 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-COX4 Neighbor (COX4NB) antibodyCOX4NB 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal 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
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- COX4NB (COX4 Neighbor (COX4NB))
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别名
- Cox4nb
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背景
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Synonyms: C16orf4, COX4 neighbor, Neighbor of COX4, COX4AL, Cox4nb, CX4NB_HUMAN, Neighbor of COX4, NOC4, EMC8, C16orf2, Protein FAM158B.
Background: COX4NB 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.
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基因ID
- 10328
抗原
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