PEX1 anticorps (Middle Region)

N° du produit ABIN954094

Détail du produit anti-PEX1 anticorps

Antigène: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Épitope: AA 606-637, Middle Region

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX1 est non-conjugé

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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

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.

Détails sur PEX1

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