SPG7 anticorps (AA 71-120)

N° du produit ABIN7231494

Cet anticorps anti-SPG7 Polyclonal Lapin (ABIN7231494) détecte spécifiquement SPG7 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour SPG7 anticorps (AA 71-120) (ABIN7231494)

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SPG7 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-SPG7 anticorps

Épitope: AA 71-120

Fonction: Rabbit Anti-SPG7 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of SPG7 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from part region of human SPG7 protein at AA range: 71-120

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur SPG7

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Autre désignation: SPG7

Sujet: Paraplegin, Cell matrix adhesion regulator, Spastic paraplegia 7 proteinSPG7 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 SPG7 cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.

Poids moléculaire: 87kD

ID gène: 6687

UniProt: Q9UQ90