PMPCA anticorps

N° du produit ABIN6572100

Détail du produit anti-PMPCA anticorps

Antigène: PMPCA (Peptidase (Mitochondrial Processing) alpha (PMPCA))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PMPCA est non-conjugé

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogène: Recombinant protein of human PMPCA

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

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: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur PMPCA

Antigène: PMPCA (Peptidase (Mitochondrial Processing) alpha (PMPCA))

Autre désignation: PMPCA (PMPCA Produits)

Synonymes: anticorps Alpha-MPP, anticorps INPP5E, anticorps 1200002L24Rik, anticorps 4933435E07Rik, anticorps P-55, anticorps wu:fi19e06, anticorps wu:fj83d11, anticorps zgc:101647, anticorps MGC114896, anticorps DKFZp459H0315, anticorps peptidase, mitochondrial processing alpha subunit, anticorps peptidase (mitochondrial processing) alpha, anticorps peptidase (mitochondrial processing) alpha S homeolog, anticorps PMPCA, anticorps Pmpca, anticorps pmpca, anticorps pmpca.S

Sujet:

Synonyms: 1200002L24Rik,4933435E07Rik,Alpha MPP,Alpha-MPP,FLJ26258,Inositol polyphosphate 5 phosphatase, 72 kD,INPP5E,KIAA0123,MGC104197,MGC93916,Mitochondrial matrix processing protease, alpha subunit,mitochondrial processing peptidase subunit alpha,Mitochondrial-processing peptidase subunit alpha,MPPA,P 55,P-55,Peptidase (mitochondrial processing) alpha,pmpca,RP11-413M3.1,RP23-306D20.8,SCAR2

Background: The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2.

Poids moléculaire:

Observed_MW: 110kDa

Calculated_MW: 44kDa/58kDa

ID gène: 23203

UniProt: Q10713

Pathways: Inositol Metabolic Process, SARS-CoV-2 Protein Interactome