TIMM8A/DDP anticorps (AA 1-50)

N° du produit ABIN7451527

Cet anticorps Lapin Polyclonal détecte spécifiquement TIMM8A/DDP dans IP. Il présente une réactivité envers Humain.

Aperçu rapide pour TIMM8A/DDP anticorps (AA 1-50) (ABIN7451527)

Antigène: TIMM8A/DDP (TIMM8A) (Translocase of Inner Mitochondrial Membrane 8A (TIMM8A))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TIMM8A/DDP est non-conjugé

Application: Immunoprecipitation (IP)

Détail du produit anti-TIMM8A/DDP anticorps

Épitope: AA 1-50

Fonction: Rabbit anti-TIMM8A Antibody, Affinity Purified

Purification: Affinity Purified

Immunogène: Between AA 1 and 50

Isotype: IgG

Information d'application

Indications d'application:

IP: 2 - 10 μg/mg lysate

WB: Not recommended

Restrictions: For Research Use only

Stockage

Concentration: 1000 μg/mL

Buffer: Tris-citrate/phosphate buffer, pH 7 to 8 containing 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: 4 °C

Date de péremption: 12 months

Détails sur TIMM8A/DDP

Antigène: TIMM8A/DDP (TIMM8A) (Translocase of Inner Mitochondrial Membrane 8A (TIMM8A))

Autre désignation: TIMM8A

Sujet: Background: Translocase of inner mitochondrial membrane 8 homolog A (TIMM8A) is a translocase involved in the import and insertion of hydrophobic membrane proteins from the cytoplasm into the mitochondrial inner membrane. The TIMM8A gene is mutated in Mohr-Tranebjaerg syndrome/Deafness Dystonia Syndrome (MTS/DDS), and it is postulated that MTS/DDS is a mitochondrial disease caused by a defective mitochondrial protein import system. Defects in the TIMM8A gene also cause Jensen syndrome, an X-linked disease with opticoacoustic nerve atrophy and muscle weakness. Along with TIMM13, TIMM8A forms a 70 kDa heterohexamer [taken from NCBI Entrez Gene (Gene ID: 1678)].

ID gène: 1678

NCBI Accession: NP_004076

UniProt: O60220