IDI1 抗体 (AA 31-130)
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- 抗原 See all IDI1 抗体
- IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))
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抗原表位
- AA 31-130
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适用
- 人, 小鼠
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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 IDI1 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)), Immunoprecipitation (IP), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 人, 小鼠
- 预测反应
- Rat,Cow,Pig,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human IDI1
- 亚型
- IgG
- Top Product
- Discover our top product IDI1 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
IP(1-2 μg) - 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
- IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))
- 别名
- IDI1 (IDI1 产品)
- 别名
- zgc:114138 antibody, 4832416K17Rik antibody, ipp1 antibody, ippl1 antibody, IPP1 antibody, IPPI1 antibody, isopentenyl-diphosphate delta isomerase 1 antibody, isopentenyl-diphosphate delta isomerase antibody, isopentenyl-diphosphate delta isomerase 1 L homeolog antibody, idi1 antibody, Idi1 antibody, idi1.L antibody, IDI1 antibody
- 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.
- 基因ID
- 3422
- UniProt
- Q13907
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