Frataxin 抗体 (AA 20-210)
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Quick Overview for Frataxin 抗体 (AA 20-210) (ABIN7871845)
抗原
See all Frataxin (FXN) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 20-210
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原理
- FXN Antibody / Frataxin
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纯化方法
- Immunogen affinity purified
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免疫原
- E.coli-derived human FXN recombinant protein (Position: Q20-A210) was used as the immunogen for the FXN antibody.
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亚型
- IgG
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anti-Frataxin (FXN) (AA 57-210) antibody
FXN 适用: 人 WB, IHC 宿主: 小鼠 Monoclonal FXN-2124 unconjugated
anti-Frataxin (FXN) (AA 91-200) antibodyFXN 适用: 人 WB, ELISA, RNAi 宿主: 小鼠 Monoclonal 3G9 unconjugated
anti-Frataxin (FXN) (AA 91-200) antibodyFXN 适用: 人 WB, ELISA, IP 宿主: 小鼠 Monoclonal 1D9 unconjugated
anti-Frataxin (FXN) (AA 143-172), (C-Term) antibodyFXN 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB12571 unconjugated
anti-Frataxin (FXN) (AA 72-102) antibodyFXN 适用: 人 WB, IF, IHC (p) 宿主: 兔 Polyclonal RB12541 unconjugated
anti-Frataxin (FXN) (AA 36-64), (N-Term) antibodyFXN 适用: 人 WB 宿主: 兔 Polyclonal RB41914 unconjugated
anti-Frataxin (FXN) (AA 41-207) antibodyFXN 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Frataxin (FXN) (AA 105-154) antibodyFXN 适用: 人, 小鼠, 大鼠, Cow, 马, 兔, 犬, 豚鼠, 猴, Pig, Bat WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Frataxin (FXN) (Internal Region) antibodyFXN 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Frataxin (FXN) (AA 1-210) antibodyFXN 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- Optimal dilution of the FXN antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL
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缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the FXN antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- Frataxin (FXN)
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别名
- FXN
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背景
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FXN antibody detects Frataxin, a mitochondrial matrix protein encoded by the FXN gene on chromosome 9q21.11. Frataxin plays a fundamental role in iron-sulfur (Fe-S) cluster biogenesis, iron homeostasis, and oxidative stress protection. It is ubiquitously expressed but highly abundant in metabolically active tissues such as heart, skeletal muscle, pancreas, and neurons, where mitochondrial energy metabolism is critical. FXN belongs to the frataxin family of mitochondrial proteins and is essential for the proper function of enzymes involved in oxidative phosphorylation and the tricarboxylic acid (TCA) cycle.
FXN acts as an iron chaperone that delivers ferrous iron (Fe2+) to scaffold proteins such as ISCU for the assembly of Fe-S clusters. These clusters serve as cofactors for numerous mitochondrial enzymes, including aconitase and complex I-III components of the respiratory chain. By regulating mitochondrial iron utilization, FXN prevents toxic iron accumulation and the generation of reactive oxygen species (ROS). Co-localization studies demonstrate FXN interaction with ISCU and NFS1 within mitochondrial nucleoids, coordinating Fe-S cluster synthesis and incorporation into target proteins.
Structurally, Frataxin is a small alpha-beta fold protein with a conserved acidic ridge that binds iron ions. It belongs to the mitochondrial Fe-S cluster assembly machinery family. FXN also associates with chaperones and proteases such as HSP60 and Lon protease, maintaining protein stability and turnover in the mitochondrial matrix. It undergoes processing from a cytosolic precursor into a mature mitochondrial form via the mitochondrial targeting sequence at its N-terminus.
Functionally, FXN is crucial for cellular respiration, antioxidant defense, and metabolic balance. It supports the activity of Fe-S-dependent enzymes in the electron transport chain and modulates mitochondrial redox status. In neurons, FXN ensures energy supply and protects against oxidative stress, while in cardiac tissue, it maintains contractile efficiency by preserving mitochondrial integrity. Developmentally, FXN expression peaks during embryogenesis and early postnatal stages, coinciding with rapid mitochondrial biogenesis in growing tissues.
Loss-of-function mutations in FXN cause Friedreich's ataxia, an autosomal recessive neurodegenerative disease characterized by impaired motor coordination, cardiomyopathy, and diabetes. The deficiency leads to mitochondrial iron overload, defective Fe-S cluster assembly, and increased oxidative stress. Pathway involvement includes Fe-S cluster biosynthesis, oxidative phosphorylation, and cellular stress response. In cancer research, FXN downregulation is associated with altered metabolic reprogramming and mitochondrial dysfunction.
Immunohistochemical staining using FXN antibody shows mitochondrial localization in neurons, cardiac myocytes, and hepatocytes. The FXN antibody from NSJ Bioreagents is a reliable reagent for studying mitochondrial metabolism, iron homeostasis, and neurodegenerative disease mechanisms such as Friedreich's ataxia. -
UniProt
- Q16595
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途径
- Transition Metal Ion Homeostasis, Regulation of Cell Size
抗原
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