NAD-ME anticorps (AA 220-479)

N° du produit ABIN6143674

Détail du produit anti-NAD-ME anticorps

Antigène: NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

Épitope: AA 220-479

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NAD-ME est non-conjugé

Application: Western Blotting (WB), Immunoprecipitation (IP)

Séquence: GLYQKRDRTQ QYDDLIDEFM KAITDRYGRN TLIQFEDFGN HNAFRFLRKY REKYCTFNDD IQGTAAVALA GLLAAQKVIS KPISEHKILF LGAGEAALGI ANLIVMSMVE NGLSEQEAQK KIWMFDKYGL LVKGRKAKID SYQEPFTHSA PESIPDTFED AVNILKPSTI IGVAGAGRLF TPDVIRAMAS INERPVIFAL SNPTAQAECT AEEAYTLTEG RCLFASGSPF GPVKLTDGRV FTPGQGNNVY IFPGYRIPIC

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 220-479 of human ME2 (NP_001161807.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IP,1:50 - 1:200

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

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 NAD-ME

Antigène: NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

Autre désignation: ME2 (NAD-ME Produits)

Synonymes: anticorps ODS1, anticorps AW120568, anticorps D030040L20Rik, anticorps NAD-ME, anticorps zgc:100941, anticorps malic enzyme 2, anticorps malic enzyme 2, NAD(+)-dependent, mitochondrial, anticorps malic enzyme 2, NAD(+)-dependent, mitochondrial S homeolog, anticorps ME2, anticorps Me2, anticorps me2.S, anticorps me2

Sujet: This gene encodes a mitochondrial NAD-dependent malic enzyme, a homotetrameric protein, that catalyzes the oxidative decarboxylation of malate to pyruvate. It had previously been weakly linked to a syndrome known as Friedreich ataxia that has since been shown to be the result of mutation in a completely different gene. Certain single-nucleotide polymorphism haplotypes of this gene have been shown to increase the risk for idiopathic generalized epilepsy. Alternatively spliced transcript variants encoding different isoforms found for this gene.,ME2,ODS1,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Warburg Effect,ME2

Poids moléculaire: 53 kDa/65 kDa

ID gène: 4200

UniProt: P23368

Pathways: Production of Molecular Mediator of Immune Response