PEX1 anticorps (AA 1049-1256)

N° du produit ABIN968642

L’anticorps Souris Monoclonal anti-PEX1 a été validé pour WB et IF. Il convient pour détecter PEX1 dans des échantillons de Humain, Souris, Rat, Chien et Poulet. Il y a 3+ publications disponibles.

Aperçu rapide pour PEX1 anticorps (AA 1049-1256) (ABIN968642)

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

Reactivité: Humain, Souris, Rat, Chien, Poulet

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp PEX1 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Clone: 1-PEX

Détail du produit anti-PEX1 anticorps

Épitope: AA 1049-1256

Réactivité croisée: Souris, Rat (Rattus), Poulet, Chien

Attributs du produit: 1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
2. Please refer to us for technical protocols.
3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.

Purification: The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.

Immunogène: Human PEX1 aa. 1049-1256

Isotype: IgG1

Information d'application

Commentaires:

Related Products: ABIN968551, ABIN967389

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 250 μg/mL

Buffer: Aqueous buffered solution containing BSA, glycerol, and ≤0.09 % 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: -20 °C

Stockage commentaire: Store undiluted at -20° C.

Références pour anticorps anti-PEX1 (ABIN968642)

Collins, Gould: "Identification of a common PEX1 mutation in Zellweger syndrome." dans: Human mutation, Vol. 14, Issue 1, pp. 45-53, (1999) (PubMed).

Geisbrecht, Collins, Reuber, Gould: "Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 95, Issue 15, pp. 8630-5, (1998) (PubMed).

Reuber, Germain-Lee, Collins, Morrell, Ameritunga, Moser, Valle, Gould: "Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders." dans: Nature genetics, Vol. 17, Issue 4, pp. 445-8, (1997) (PubMed).

Détails sur PEX1

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

Autre désignation: PEX1

Sujet: Peroxisomes, ubiquitous organelles of eukaryotic cells, are involved in a number of metabolic processes. Their formation involves membrane generation, targeting and insertion of peroxisomal membrane proteins (PMPs) into the membrane, and transport of matrix proteins across the newly formed membrane. Import of PMPs and synthesis of peroxisomal membranes may involve as many as 17 different PEX proteins. Mutation in any of 12 different Pex genes causes Zellweger syndrome (ZS), a disease characterized by loss of peroxisome biogenesis leading to severe neurologic, hepatic, and renal abnormalities. Mutations in two peroxisomal AAA ATPases, PEX1 and PEX6, are commonly associated with this and other neurological disorders. These ATPases form a complex in vitro and are required for normal import of proteins targeted to the peroxisome, as well as for maintaining the stability of PEX5, a peroxisomal receptor required for protein import. Substitution of aspartate for glycine at position 843 in PEX1 is the most common cause of peroxisome biogenesis disorders. Thus, PEX1 has an essential role in peroxisome biogenesis and mutation leads to Zwellweger syndrome-type diseases. This antibody is routinely tested by western blot analysis.

Poids moléculaire: 143 kDa