PPOX 抗体 (N-Term)
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- 抗原 See all PPOX 抗体
- PPOX (Protoporphyrinogen Oxidase (PPOX))
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抗原表位
- N-Term
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适用
- 人, 小鼠, 大鼠
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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 PPOX antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 特异性
- PPOX antibody was raised against the N terminal of PPOX
- 纯化方法
- Affinity purified
- 免疫原
- PPOX antibody was raised using the N terminal of PPOX corresponding to a region with amino acids SSERLGGWIRSVRGPNGAIFELGPRGIRPAGALGARTLLLVSELGLDSEV
- Top Product
- Discover our top product PPOX Primary Antibody
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- 应用备注
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WB: 1 µg/mL
Optimal conditions should be determined by the investigator. - 说明
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PPOX Blocking Peptide, catalog no. 33R-8796, is also available for use as a blocking control in assays to test for specificity of this PPOX antibody
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of PPOX antibody in PBS
- 浓度
- Lot specific
- 缓冲液
- PBS
- 注意事项
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Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use. - 储存条件
- 4 °C/-20 °C
- 储存方法
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
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- 抗原
- PPOX (Protoporphyrinogen Oxidase (PPOX))
- 别名
- PPOX (PPOX 产品)
- 别名
- PPO antibody, V290M antibody, VP antibody, Ppo antibody, BcDNA:LD41392 antibody, CG5796 antibody, Dmel\\CG5796 antibody, ESTS:9F2T antibody, zgc:123252 antibody, HEMG1 antibody, PPO1 antibody, PROTOPORPHYRINOGEN OXIDASE antibody, TC0121 antibody, hemG antibody, protoporphyrinogen oxidase antibody, Protoporphyrinogen oxidase antibody, Flavin containing amine oxidoreductase family antibody, polyphenol oxidase, chloroplastic antibody, PPOX antibody, Ppox antibody, ppox antibody, hemY antibody, TC_RS00645 antibody, Mrub_1406 antibody, Mesil_2992 antibody, Trad_0583 antibody, Calni_0746 antibody, Ocepr_1049 antibody, Tmar_0766 antibody, Intca_1907 antibody, Despr_0642 antibody, Plabr_2407 antibody, Deipr_2130 antibody, Hipma_0622 antibody, LOC110782963 antibody
- 背景
- This gene encodes the penultimate enzyme of heme biosynthesis, which catalyzes the 6-electron oxidation of protoporphyrinogen IX to form protoporphyrin IX. Mutations in this gene cause variegate porphyria, an autosomal dominant disorder of heme metabolism resulting from a deficiency in protoporphyrinogen oxidase, an enzyme located on the inner mitochondrial membrane. Alternatively spliced transcript variants encoding the same protein have been identified.
- 分子量
- 51 kDa (MW of target protein)
- 途径
- Synaptic Membrane, Feeding Behaviour
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