IDI1 抗体
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- 抗原 See all IDI1 抗体
- IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))
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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 IDI1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人
- 产品特性
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Rabbit polyclonal antibody to IDI1 (isopentenyl-diphosphate delta isomerase 1)
IDI1 antibody [N1C2] - 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human IDI1. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product IDI1 Primary Antibody
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- 应用备注
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
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Positive Control: Molt-4
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.65 mg/mL
- 缓冲液
- 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): 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
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))
- 别名
- isopentenyl-diphosphate delta isomerase 1 (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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IDI1 encodes a peroxisomally-localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP), which are the substrates for the successive reaction that results in the synthesis of farnesyl diphosphate and, ultimately, cholesterol. It has been shown in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy that there is reduction in IPP isomerase activity.
Cellular Localization: Peroxisome - 分子量
- 26 kDa
- 基因ID
- 3422
- UniProt
- Q13907
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