PEX1 anticorps (AA 599-628)
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- Antigène Voir toutes PEX1 Anticorps
- PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))
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Épitope
- AA 599-628
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp PEX1 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- This PEX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 599-628 amino acids from the Central region of human PEX1.
- Clone
- RB23674
- Isotype
- Ig Fraction
- Top Product
- Discover our top product PEX1 Anticorps primaire
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- Indications d'application
- WB: 1:1000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
- Date de péremption
- 6 months
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- Antigène
- PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))
- Autre désignation
- PEX1 (PEX1 Produits)
- Synonymes
- anticorps PBD1A, anticorps PBD1B, anticorps ZWS, anticorps ZWS1, anticorps 5430414H02Rik, anticorps E330005K07Rik, anticorps RGD1559939, anticorps pex1, anticorps peroxisomal biogenesis factor 1, anticorps peroxisomal biogenesis factor 1 L homeolog, anticorps PEX1, anticorps Pex1, anticorps pex1.L
- Sujet
- This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome.
- Poids moléculaire
- 142867
- ID gène
- 5189
- NCBI Accession
- NP_000457
- UniProt
- O43933
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