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- Tel: 858.663.9055
- Email: info@nsjbio.com
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Frataxin is a nuclear-encoded mitochondrial protein implicated in Friedreich's ataxia (FRDA), a human autosomal recessive neurodegenerative disease. Lack of Frataxin causes iron to accumulate in the mitochondrial matrix suggesting that Frataxin is involved in mitochondrial iron homeostasis and possibly in iron transport. Frataxin has an alpha-beta fold consisting of two helices flanking an antiparallel beta sheet.
Optimal dilution of the recombinant Frataxin antibody should be determined by the researcher.
Amino acids 57-210 from the human protein were used as the immunogen for this FXN antibody.
Store the recombinant Frataxin antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
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