AFG3L2 anticorps

N° du produit ABIN4950041

Détail du produit anti-AFG3L2 anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AFG3L2 est non-conjugé

Application: Western Blotting (WB)

Purification: Antigen affinity

Immunogène: Amino acids R168-D250 of the human protein were used as the immunogen for the AFG3L2 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the AFG3L2 antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL

Restrictions: For Research Use only

Stockage

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

Stock: -20 °C

Stockage commentaire: After reconstitution, the AFG3L2 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Détails sur AFG3L2

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

Autre désignation: AFG3L2 (AFG3L2 Produits)

Synonymes: anticorps MGC147390, anticorps si:ch211-12e1.4, anticorps SCA28, anticorps SPAX5, anticorps 2310036I02Rik, anticorps AW260507, anticorps Emv66, anticorps par, anticorps AFG3 like matrix AAA peptidase subunit 2, anticorps AFG3-like protein 2, anticorps AFG3 ATPase family gene 3-like 2 (S. cerevisiae), anticorps AFG3-like AAA ATPase 2, anticorps AFG3-like AAA ATPase 2 L homeolog, anticorps AFG3L2, anticorps LOC578526, anticorps afg3l2, anticorps afg3l2.L, anticorps 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.

UniProt: Q9Y4W6

Pathways: Skeletal Muscle Fiber Development