IDI1 抗体 (AA 31-130) (FITC)
Quick Overview for IDI1 抗体 (AA 31-130) (FITC) (ABIN709278)
抗原
See all IDI1 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 31-130
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交叉反应
- 人, 小鼠
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预测反应
- Rat,Cow,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 IDI1
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亚型
- IgG
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anti-Isopentenyl-Diphosphate delta Isomerase 1 (IDI1) (AA 175-283) antibody
IDI1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 6G10 unconjugated
anti-Isopentenyl-Diphosphate delta Isomerase 1 (IDI1) antibodyIDI1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Isopentenyl-Diphosphate delta Isomerase 1 (IDI1) (AA 1-228) antibodyIDI1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Isopentenyl-Diphosphate delta Isomerase 1 (IDI1) (AA 175-283) antibodyIDI1 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Isopentenyl-Diphosphate delta Isomerase 1 (IDI1) (AA 1-228) antibodyIDI1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Isopentenyl-Diphosphate delta Isomerase 1 (IDI1) (AA 146-195) antibodyIDI1 适用: 人, 小鼠, 大鼠, 豚鼠, 马, Hamster WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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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
- 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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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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- IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))
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别名
- IDI1
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背景
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Synonyms: IDI1, IPP isomerase 1, IPPI1, Isopentenyl diphosphate Delta isomerase 1, isopentenyl diphosphate dimethylallyl diphosphate isomerase 1, Isopentenyl pyrophosphate isomerase 1, IDI1_HUMAN.
Background: IDI1 is a peroxisomally localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP). These are substrates for the reactions that ultimately result in the synthesis of cholesterol. There is reduction in IPP isomerase activity in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy.
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基因ID
- 3422
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UniProt
- Q13907
抗原
-
