NDUFB3 anticorps (AA 1-98)

N° du produit ABIN7268810

Détail du produit anti-NDUFB3 anticorps

Antigène: NDUFB3 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 3, 12kDa (NDUFB3))

Épitope: AA 1-98

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NDUFB3 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Fonction: NDUFB3 Rabbit pAb

Séquence: MAHEHGHEHG HHKMELPDYR QWKIEGTPLE TIQKKLAAKG LRDPWGRNEA WRYMGGFAKS VSFSDVFFKG FKWGFAAFVV AVGAEYYLES LNKDKKHH

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-98 of human NDUFB3 (NP_002482.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IF,1:50 - 1:100

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 NDUFB3

Antigène: NDUFB3 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 3, 12kDa (NDUFB3))

Autre désignation: NDUFB3 (NDUFB3 Produits)

Synonymes: anticorps NDUFB3, anticorps 2700033I16Rik, anticorps AI415450, anticorps B12, anticorps CI-B12, anticorps NADH:ubiquinone oxidoreductase subunit B3, anticorps NADH:ubiquinone oxidoreductase subunit B3 S homeolog, anticorps NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa, anticorps NADH dehydrogenase (ubiquinone) 1 beta subcomplex 3, anticorps Ndufb3, anticorps NDUFB3, anticorps ndufb3.S, anticorps ndufb3

Sujet: This gene encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria. This protein localizes to the inner membrane of the mitochondrion as a single-pass membrane protein. Mutations in this gene contribute to mitochondrial complex 1 deficiency. Alternative splicing results in multiple transcript variants encoding the same protein. Humans have multiple pseudogenes of this gene.,NDUFB3,B12,CI-B12,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Oxidative phosphorylation,Neuroscience,Neurodegenerative Diseases,NDUFB3

Poids moléculaire: 11kDa

ID gène: 4709

UniProt: O43676