FECH 抗体 (AbBy Fluor® 488)
Quick Overview for FECH 抗体 (AbBy Fluor® 488) (ABIN1403206)
抗原
See all FECH 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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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 EPB41
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亚型
- IgG
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anti-Ferrochelatase (FECH) (AA 1-200) antibody
FECH 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Ferrochelatase (FECH) (AA 55-423) antibodyFECH 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Ferrochelatase (FECH) antibodyFECH 适用: 人, 小鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Ferrochelatase (FECH) (AA 1-423) antibodyFECH 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Ferrochelatase (FECH) (C-Term) antibodyFECH 适用: 人, 小鼠, 大鼠 WB, IHC, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Ferrochelatase (FECH) (AA 51-100) antibodyFECH 适用: 人, 兔, 猴 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Ferrochelatase (FECH) (N-Term) antibodyFECH 适用: 人, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Ferrochelatase (FECH) (N-Term) antibodyFECH 适用: 人, 小鼠, 大鼠, 犬, 兔, Cow, 豚鼠, 马, 斑马鱼, Saccharomyces cerevisiae WB 宿主: 兔 Polyclonal unconjugated
anti-Ferrochelatase (FECH) (AA 252-301) antibodyFECH 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Ferrochelatase (FECH) (AA 314-423) antibodyFECH 适用: 人 ELISA 宿主: 小鼠 Monoclonal 3H3 unconjugated
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应用备注
- IF(IHC-P) 1:50-200
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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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- FECH (Ferrochelatase (FECH))
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别名
- FECH
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背景
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Synonyms: EPP, FCE, Ferrochelatase protoporphyria, Ferrochelatase, Ferrochelatase mitochondrial, Heme synthetase, Protoheme ferro lyase, HEMH_HUMAN.
Background: Ferrochelatase catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway, and is localised in the mitochondrion. Defects in ferrochelatase are associated with protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. Porphyrias are a group of inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). They are broadly classified as hepatic porphyrias or erythropoietic porphyrias, based on the site of the overproduction and mainly accumulation of the porphyrins (or their chemical precursors). They manifest with either skin problems, or neurological complications, or occasionally both.
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基因ID
- 2235
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途径
- Transition Metal Ion Homeostasis
抗原
-
