UROD 抗体 (AA 121-220) (Cy5.5)
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- 抗原 See all UROD 抗体
- UROD (Uroporphyrinogen Decarboxylase (UROD))
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抗原表位
- AA 121-220
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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 UROD antibody is conjugated to Cy5.5
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human UROD
- 亚型
- IgG
- Top Product
- Discover our top product UROD Primary Antibody
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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
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- UROD (Uroporphyrinogen Decarboxylase (UROD))
- 别名
- UROD (UROD 产品)
- 别名
- UROD antibody, pct antibody, wu:fc43e09 antibody, PCT antibody, UPD antibody, AI323803 antibody, Uro-d antibody, porphyrinogen carboxy-lyase antibody, uroporphyrinogen decarboxylase antibody, Uroporphyrinogen decarboxylase UroD antibody, Uroporphyrinogen decarboxylase antibody, UROD antibody, urod antibody, hemE antibody, uroD antibody, Cpin_6502 antibody, Rmar_1187 antibody, LOC5568261 antibody, Mrub_1403 antibody, Arnit_2230 antibody, Ndas_2830 antibody, Mesil_2989 antibody, Trad_0222 antibody, Weevi_0432 antibody, Hipma_1229 antibody, Fluta_0529 antibody, Marky_1143 antibody, Halhy_5610 antibody, Mesop_0899 antibody, Ccan_20670 antibody, Urod antibody
- 背景
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Synonyms: PCT, UPD, URO D, Uroporphyrinogen decarboxylase, Uroporphyrinogen III decarboxylase.
Background: UROD is the fifth enzyme of the heme biosynthetic pathway. This enzyme is responsible for catalyzing the conversion of uroporphyrinogen to coproporphyrinogen through the removal of four carboxymethyl side chains. Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoetic porphyria. Porphyria cutanea tarda is an autosomal dominant disorder characterized by light-sensitive dermatitis and associated with the excretion of large amounts of uroporphyrin in urine. Hepatoerythropoetic porphyria is a form of porphyria cutanae tarda that may also be a manifestation of benign or malignant hepatic tumors.
- 基因ID
- 79842
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