AFG3L2 anticorps (AA 161-245)

N° du produit ABIN7825258

L’anticorps anti-AFG3L2 Polyclonal produit chez le Lapin a été validé pour WB. Il convient pour la détection de AFG3L2 dans des échantillons provenant de Poisson zèbre (Danio rerio). }

Aperçu rapide pour AFG3L2 anticorps (AA 161-245) (ABIN7825258)

Antigène: AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

Reactivité: Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AFG3L2 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-AFG3L2 anticorps

Épitope: AA 161-245

Fonction: Anti-Zebrafish AFG3L2 Antibody

Attributs du produit: Anti-Zebrafish AFG3L2 Antibody catalog # AZA9JRG9. Tested in WB applications. This antibody reacts with Zebrafish. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived zebrafish AFG3L2 recombinant protein (Position: G161-D245).

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Zebrafish

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur AFG3L2

Antigène: AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

Autre désignation: AFG3L2

Sujet: AFG3L2 is the catalytic subunit of the m-AAA protease, an ATP-dependent proteolytic complex of the mitochondrial inner membrane that degrades misfolded proteins and regulates ribosome assembly. In humans, it is encoded by the AFG3L2 gene. This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. And this gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders as well as spastic ataxia-neuropathy syndrome.

ID gène: 569168

Pathways: Skeletal Muscle Fiber Development