GFOD2 抗体 (AA 301-385) (HRP)
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北京 101111
Quick Overview for GFOD2 抗体 (AA 301-385) (HRP) (ABIN1416766)
抗原
See all GFOD2 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 301-385
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预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,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 GFOD2
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亚型
- IgG
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anti-Glucose-Fructose Oxidoreductase Domain Containing 2 (GFOD2) (AA 1-280) antibody
GFOD2 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Glucose-Fructose Oxidoreductase Domain Containing 2 (GFOD2) (AA 198-385) antibodyGFOD2 适用: 人 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Glucose-Fructose Oxidoreductase Domain Containing 2 (GFOD2) (AA 1-280) antibodyGFOD2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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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注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- GFOD2 (Glucose-Fructose Oxidoreductase Domain Containing 2 (GFOD2))
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别名
- GFOD2
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背景
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Synonyms: GFOD2, GFOD2_HUMAN, Glucose fructose oxidoreductase domain containing 2, Glucose fructose oxidoreductase domain containing protein 2, Glucose-fructose oxidoreductase domain-containing protein 2, MGC11335.
Background: GFOD2 is a 385 amino acid secreted protein of the extracellular matrix that belongs to the gfo/idh/mocA family. Existing as two alternatively spliced isoforms, GFOD2 enhances matrix assembly and is encoded by a gene that maps to human chromosome 16q22.1. Chromosome 16 encodes over 900 genes and comprises nearly 3 % of the human genome. 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, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
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基因ID
- 81577
抗原
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