SPG20 anticorps (AA 205-631)

N° du produit ABIN7872097

Cet anticorps anti-SPG20 Polyclonal Lapin (ABIN7872097) détecte spécifiquement SPG20 dans WB, ELISA et FACS. L’anticorps est réactif avec des échantillons de Humain et Rat.

Aperçu rapide pour SPG20 anticorps (AA 205-631) (ABIN7872097)

Antigène: SPG20 (Spastic Paraplegia 20 (Troyer Syndrome) (SPG20))

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SPG20 est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Détail du produit anti-SPG20 anticorps

Épitope: AA 205-631

Fonction: Spartin Antibody / SPART

Purification: Antigen affinity purified

Immunogène: Recombinant human protein (amino acids H205-V631) was used as the immunogen for the Spartin antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Spartin 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 Spartin 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 SPG20

Antigène: SPG20 (Spastic Paraplegia 20 (Troyer Syndrome) (SPG20))

Autre désignation: Spartin

Sujet: Spartin is a protein that in humans is encoded by the SPART gene. This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome).

UniProt: Q8N0X7

Pathways: Regulation of Cell Size, SARS-CoV-2 Protein Interactome