SPG7 anticorps (AA 115-141)

N° du produit ABIN656408

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

Aperçu rapide pour SPG7 anticorps (AA 115-141) (ABIN656408)

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))

Clone: RB23654

Détail du produit anti-SPG7 anticorps

Épitope: AA 115-141

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This SPG7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 115-141 amino acids from the Central region of human SPG7.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in 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.

Stock: 4 °C,-20 °C

Stockage commentaire: SPG7 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Date de péremption: 6 months

Détails sur SPG7

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Autre désignation: SPG7

Sujet: This 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. [provided by RefSeq].

Poids moléculaire: 88235

ID gène: 6687

NCBI Accession: NP_003110, NP_955399

UniProt: Q9UQ90