SPG7 anticorps (N-Term)

N° du produit ABIN5515659

Cet anticorps Lapin Polyclonal détecte spécifiquement SPG7 dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour SPG7 anticorps (N-Term) (ABIN5515659)

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SPG7 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SPG7 anticorps

Épitope: N-Term

Fonction: SPG7 Antibody - N-terminal region

Séquence: LWQLLGGTFY FNTSRLKQKN KEKDKSKGKA PEEDEEERRR RERDDQMYRE

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human SPG7

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP81354-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur SPG7

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Autre désignation: SPG7

Sujet:

Background Information: This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.

Gene Name: spastic paraplegia 7 (pure and complicated autosomal recessive)

Alternative Symbols: CAR, PGN, CMAR, SPG5C

Protein Name: paraplegin

Poids moléculaire: 53 kDa

ID gène: 6687

NCBI Accession: NP_003110

UniProt: Q9UQ90