UBIAD1 抗体 (C-Term)
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Quick Overview for UBIAD1 抗体 (C-Term) (ABIN6991991)
抗原
See all UBIAD1 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 210-260, C-Term
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特异性
- UBIAD1 antibody is human, mouse and rat reactive.
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纯化方法
- UBIAD1 antibody is affinity chromatography purified via peptide column.
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免疫原
- UBIAD1 antibody was raised against a 15 amino acid peptide near the carboxy terminus of human UBIAD1. The immunogen is located within amino acids 210 - 260 of UBIAD1.
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亚型
- IgG
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anti-UbiA Prenyltransferase Domain Containing 1 (UBIAD1) (AA 1-100) antibody
UBIAD1 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-UbiA Prenyltransferase Domain Containing 1 (UBIAD1) (AA 1-100) antibodyUBIAD1 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-UbiA Prenyltransferase Domain Containing 1 (UBIAD1) (AA 1-82) antibodyUBIAD1 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
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应用备注
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UBIAD1 antibody can be used for detection of UBIAD1 by Western blot at 1 - 2 μ,g/mL. Antibody can also be used for Immunohistochemistry at 5 μ,g/mL. For Immunoflorescence start at 20 μ,g/mL.
Antibody validated: Western Blot in mouse samples, Immunohistochemistry in mouse samples and Immunofluorescence in mouse samples. All other applications and species not yet tested. -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- UBIAD1 Antibody is supplied in PBS containing 0.02 % sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C,4 °C
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储存方法
- UBIAD1 antibody can be stored at 4°C for three months and -20°C, stable for up to one year.
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- UBIAD1 (UbiA Prenyltransferase Domain Containing 1 (UBIAD1))
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别名
- UBIAD1
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背景
- The UbiA prenyltransferase domain containing 1 (UBIAD1) protein , also known as TERE1, was initially identified as a down-regulated gene in transitional cell carcinoma of the bladder (1). Recently it has been shown to bind the cholesterol carrier APOE and modulate cellular cholesterol levels (2). Mutations in the UBIAD1 gene can cause Schnyder crystalline corneal dystrophy, an autosomal dominant disease characterized by progressive opacification of the cornea resulting from the local accumulation of lipids (3).
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分子量
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Predicted: 37 kDa
Observed: 45 kDa -
基因ID
- 29914
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NCBI登录号
- NP_037451
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UniProt
- Q9Y5Z9
抗原
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