SPG7 anticorps (AA 71-120)

N° du produit ABIN7231494

Cet anticorps anti-SPG7 est un anticorps Lapin Polyclonal détectant SPG7 dans WB et ELISA. Adapté pour Humain.

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

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Reactivité: Humain

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: SPG7 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of SPG7 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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 (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: -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.

Détails sur SPG7

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Autre désignation: SPG7

Sujet: Rabbit Anti-SPG7 Polyclonal Antibody,Paraplegin, Cell matrix adhesion regulator, Spastic paraplegia 7 protein,SPG7 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.,SPG7

Poids moléculaire: observerd band 87kDa

ID gène: 6687

UniProt: Q9UQ90