SPG7 anticorps (AA 115-141)

N° du produit ABIN656408

Détail du produit anti-SPG7 anticorps

Antigène: SPG7 (Spastic Paraplegia 7 (SPG7))

Épitope: AA 115-141

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SPG7 est non-conjugé

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

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.

Clone: RB23654

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 (SPG7 Produits)

Synonymes: anticorps CAR, anticorps CMAR, anticorps PGN, anticorps SPG5C, anticorps AI452278, anticorps AU015315, anticorps Cmar, anticorps SPG7, paraplegin matrix AAA peptidase subunit, anticorps SPG7, anticorps 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