PEX1 抗体
PEX1 抗体 by Grade
Find PEX1 抗体 with a specific Grade. The Grade listed below are among those available. Click on a link to go to the corresponding products.
PEX1 抗体 by 适用
Find PEX1 抗体 for a variety of species such as anti-Human PEX1, anti-Mouse PEX1, anti-Rat PEX1. The species listed below are among those available. Click on a link to go to the corresponding products.
PEX1 抗体 by 应用范围
Find PEX1 抗体 validated for a specific application such as ELISA, WB, IHC, ICC. Some of the available applications are listed below. Click on a link to go to the corresponding products.
PEX1 抗体 by 抗体来源
Find PEX1 抗体 with a specific 抗体来源. The 抗体来源 listed below are among those available. Click on a link to go to the corresponding products.
PEX1 抗体 by 克隆形成能力
Find available monoclonal or polyclonal PEX1 抗体. Click on a link to go to the corresponding products.
PEX1 抗体 by 克隆
Find PEX1 抗体 with a specific 克隆. The 克隆 listed below are among those available. Click on a link to go to the corresponding products.
PEX1 抗体 by 标记
Find PEX1 抗体 with a specific conjugate such as Biotin, FITC, HRP. The conjugates listed below are among those available. Click on a link to go to the corresponding products.
Popular PEX1 抗体
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Latest Publications for our PEX1 抗体
: "Peroxisomal monoubiquitinated PEX5 interacts with the AAA ATPases PEX1 and PEX6 and is unfolded during its dislocation into the cytosol." in: The Journal of biological chemistry, Vol. 293, Issue 29, pp. 11553-11563, (2019) (PubMed).: "Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders." in: Human mutation, Vol. 30, Issue 3, pp. E467-80, (2009) (PubMed).
: "Identification of a common PEX1 mutation in Zellweger syndrome." in: Human mutation, Vol. 14, Issue 1, pp. 45-53, (1999) (PubMed).
: "Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 95, Issue 15, pp. 8630-5, (1998) (PubMed).
: "Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders." in: Nature genetics, Vol. 17, Issue 4, pp. 445-8, (1997) (PubMed).
Aliases for PEX1 抗体
peroxisomal biogenesis factor 1 (PEX1) 抗体peroxisomal biogenesis factor 1 (Pex1) 抗体
peroxisomal biogenesis factor 1 L homeolog (pex1.L) 抗体
5430414H02Rik 抗体
E330005K07Rik 抗体
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