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NDUFA12 anticorps
NDUFA12
Reactivité: Humain, Souris
ELISA, IHC
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN7237961
Détail du produit anti-NDUFA12 anticorps
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Antigène
Voir toutes NDUFA12 Anticorps
NDUFA12
(NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 12 (NDUFA12))
Reactivité
Toutes les réactivités sur NDUFA12 Anticorps
Humain, Souris
Hôte
Toutes les hôtes sur NDUFA12 Anticorps
Lapin
Clonalité
Toutes les clonalités sur NDUFA12 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers NDUFA12 Anticorps
Cet anticorp NDUFA12 est non-conjugé
Application
Tous les applications à travers NDUFA12 Anticorps.
ELISA, Immunohistochemistry (IHC)
Attributs du produit
Polyclonal Antibody
Purification
Affinity purification
Immunogène
Synthetic peptide of human NDUFA12
Isotype
IgG
Top Product
Discover our top product NDUFA12 Anticorps primaire
Alternatives
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Information d'application
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Indications d'application
IHC 1:50-1:200
Restrictions
For Research Use only
Stockage
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Format
Liquid
Concentration
0.6 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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 NDUFA12
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Antigène
NDUFA12
(NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 12 (NDUFA12))
Autre désignation
NDUFA12 (NDUFA12 Produits )
Synonymes
anticorps RGD1311462, anticorps si:dkey-183c16.3, anticorps zgc:112053, anticorps B17.2, anticorps DAP13, anticorps 2410011G03Rik, anticorps AW112974, anticorps NADH:ubiquinone oxidoreductase subunit A12, anticorps NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12, anticorps Ndufa12, anticorps NDUFA12, anticorps ndufa12
Sujet
This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants.
NCBI Accession
NP_061326
UniProt
Q9UI09
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