LONP1 anticorps (AA 137-320)

N° du produit ABIN7870574

Cet anticorps Lapin Polyclonal détecte spécifiquement LONP1 dans WB, ELISA, IF, IHC (p), IP et FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour LONP1 anticorps (AA 137-320) (ABIN7870574)

Antigène: LONP1 (Lon Peptidase 1, Mitochondrial (LONP1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LONP1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunoprecipitation (IP), Flow Cytometry (FACS)

Détail du produit anti-LONP1 anticorps

Épitope: AA 137-320

Fonction: LONP1 Antibody

Purification: Affinity purified

Immunogène: Amino acids R137-A320 from the human protein were used as the immunogen for the LONP1 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the LONP1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the LONP1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur LONP1

Antigène: LONP1 (Lon Peptidase 1, Mitochondrial (LONP1))

Autre désignation: LONP1

Sujet: Lon protease homolog, mitochondrial is an enzyme that in humans is encoded by the LONP1gene. It is mapped to 19p13.3. This gene encodes a mitochondrial matrix protein that belongs to the Lon family of ATP-dependent proteases. This protein mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides in the mitochondrial matrix. It may also have a chaperone function in the assembly of inner membrane protein complexes, and participate in the regulation of mitochondrial gene expression and maintenance of the integrity of the mitochondrial genome. Decreased expression of this gene has been noted in a patient with hereditary spastic paraplegia.

UniProt: P36776