COX4NB 抗体 (AA 121-210)
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- 抗原 See all COX4NB 抗体
- COX4NB (COX4 Neighbor (COX4NB))
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抗原表位
- AA 121-210
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适用
- 人
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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 (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human COX4NB
- 亚型
- IgG
- Top Product
- Discover our top product COX4NB Primary Antibody
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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
- 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
- COX4NB (COX4 Neighbor (COX4NB))
- 别名
- Cox4nb (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
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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.
- 基因ID
- 10328
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