COG8 抗体
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- 抗原 See all COG8 抗体
- COG8 (Component of Oligomeric Golgi Complex 8 (COG8))
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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 COG8 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
- 交叉反应
- 人
- 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human COG8. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product COG8 Primary Antibody
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anti-Component of Oligomeric Golgi Complex 8 (COG8) (AA 521-612) antibody
COG8 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Component of Oligomeric Golgi Complex 8 (COG8) (AA 1-219) antibodyCOG8 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Component of Oligomeric Golgi Complex 8 (COG8) (Internal Region) antibodyVerified COG8 适用: 人 ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
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- 应用备注
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
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Positive Control: Raji
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): 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
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- COG8 (Component of Oligomeric Golgi Complex 8 (COG8))
- 别名
- component of oligomeric golgi complex 8 (COG8 产品)
- 别名
- CDG2H antibody, DOR1 antibody, BB235941 antibody, C87832 antibody, component of oligomeric golgi complex 8 antibody, Cog8 antibody, cog8 antibody, COG8 antibody
- 背景
- Component of oligomeric golgi complex 8 , CDG2H , DOR1,This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq]
- 分子量
- 68 kDa
- 基因ID
- 84342
- UniProt
- Q96MW5
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