SPG7 anticorps (Middle Region)

N° du produit ABIN953990

L’anticorps Lapin Polyclonal anti-SPG7 a été validé pour WB, IHC (p) et EIA. Il convient pour détecter SPG7 dans des échantillons de Humain.

Aperçu rapide pour SPG7 anticorps (Middle Region) (ABIN953990)

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SPG7 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Détail du produit anti-SPG7 anticorps

Épitope: AA 114-141, Middle Region

Specificité: This antibody recognizes Paraplegin / SPG7.

Réactivité croisée (Details): Species reactivity (tested):Human

Purification: Purified through a Protein A column followed by peptide affinity purification

Immunogène: Synthetic peptide - KLH conjugated - corresponding to the central region (between 114-141aa) of human Paraplegin / SPG7

Isotype: Ig Fraction

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) 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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur SPG7

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Autre désignation: Paraplegin / SPG7

Sujet: The SPG7 gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein 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. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7.Synonyms: CAR, CMAR, PGN, Spastic paraplegia 7 protein

ID gène: 6687

NCBI Accession: NP_003110