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- Product number
- ABIN968642 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Peroxisomal Biogenesis Factor 1 (PEX1) (AA 1049-1256) antibody
- Antibody type
- Monoclonal
- Antigen
- Human PEX1
- Reactivity
- Human
- Host
- Mouse
- Isotype
- IgG
- Antibody clone number
- 1
- Vial size
- 150 µg
- Concentration
- 250 µg/ml
- Storage
- Store undiluted at -20° C.
Submitted references Identification of a common PEX1 mutation in Zellweger syndrome.
Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease.
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.
Collins CS, Gould SJ
Human mutation 1999;14(1):45-53
Human mutation 1999;14(1):45-53
Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease.
Geisbrecht BV, Collins CS, Reuber BE, Gould SJ
Proceedings of the National Academy of Sciences of the United States of America 1998 Jul 21;95(15):8630-5
Proceedings of the National Academy of Sciences of the United States of America 1998 Jul 21;95(15):8630-5
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.
Reuber BE, Germain-Lee E, Collins CS, Morrell JC, Ameritunga R, Moser HW, Valle D, Gould SJ
Nature genetics 1997 Dec;17(4):445-8
Nature genetics 1997 Dec;17(4):445-8
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