GFOD2 抗体 (AA 301-385)
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- 抗原 See all GFOD2 抗体
- GFOD2 (Glucose-Fructose Oxidoreductase Domain Containing 2 (GFOD2))
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抗原表位
- AA 301-385
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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 GFOD2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GFOD2
- 亚型
- IgG
- Top Product
- Discover our top product GFOD2 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
- GFOD2 (Glucose-Fructose Oxidoreductase Domain Containing 2 (GFOD2))
- 别名
- GFOD2 (GFOD2 产品)
- 别名
- MGC107952 antibody, fa92g04 antibody, wu:fa92g04 antibody, zgc:153587 antibody, 5730466C23Rik antibody, RGD1311198 antibody, glucose-fructose oxidoreductase domain containing 2 antibody, glucose-fructose oxidoreductase domain containing 2 L homeolog antibody, GFOD2 antibody, gfod2 antibody, Gfod2 antibody, gfod2.L antibody
- 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.
- 基因ID
- 81577
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