FAHD2A 抗体 (AA 121-230)
Quick Overview for FAHD2A 抗体 (AA 121-230) (ABIN872703)
抗原
See all FAHD2A 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 121-230
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预测反应
- Human,Mouse,Rat,Horse,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 FAHD2A
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亚型
- IgG
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anti-Fumarylacetoacetate Hydrolase Domain Containing 2A (FAHD2A) (AA 4-314) antibody
FAHD2A 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Fumarylacetoacetate Hydrolase Domain Containing 2A (FAHD2A) (AA 1-314) antibodyFAHD2A 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Fumarylacetoacetate Hydrolase Domain Containing 2A (FAHD2A) (AA 28-77) antibodyFAHD2A 适用: 人, 猴 WB 宿主: 兔 Polyclonal 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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- FAHD2A (Fumarylacetoacetate Hydrolase Domain Containing 2A (FAHD2A))
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别名
- Fahd2a
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背景
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Synonyms: CGI 105, FAH2A_HUMAN, FAHD 2A, FAHD2A, Fumarylacetoacetate hydrolase domain containing 1, Fumarylacetoacetate hydrolase domain containing 2A, Fumarylacetoacetate hydrolase domain containing protein 2A, Fumarylacetoacetate hydrolase domain-containing protein 2A.
Background: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is also associated with mutations to chromosome 2.
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基因ID
- 51011
抗原
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