PEX1 anticorps (Middle Region)
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- Antigène Voir toutes PEX1 Anticorps
- PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))
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Épitope
- AA 606-637, Middle Region
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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), Enzyme Immunoassay (EIA)
- Specificité
- This antibody recognizes Human Peroxin 1 / PEX1 (Center).
- Purification
- Protein A column, followed by peptide affinity purification
- Immunogène
- KLH conjugated synthetic peptide between 606-637 amino acids from the Central region of Human Peroxin 1 / PEX1
- Isotype
- Ig Fraction
- Top Product
- Discover our top product PEX1 Anticorps primaire
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.25 mg/mL
- Buffer
- PBS containing 0.09 % (W/V) Sodium Azide as preservative
- 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.
- Conseil sur la manipulation
- Avoid repeated freezing and thawing.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Antigène
- PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))
- Autre désignation
- Peroxin 1 / 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.Synonyms: Peroxin-1, Peroxisome biogenesis disorder protein 1, Peroxisome biogenesis factor 1
- Poids moléculaire
- 142867 Da
- ID gène
- 5189
- NCBI Accession
- NP_000457
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