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ALDH5A1 anticorps
ALDH5A1
Reactivité: Humain, Rat, Souris
ELISA, IHC
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN7238516
Détail du produit anti-ALDH5A1 anticorps
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Antigène
Voir toutes ALDH5A1 Anticorps
ALDH5A1
(Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))
Reactivité
Toutes les réactivités sur ALDH5A1 Anticorps
Humain, Rat, Souris
Hôte
Toutes les hôtes sur ALDH5A1 Anticorps
Lapin
Clonalité
Toutes les clonalités sur ALDH5A1 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers ALDH5A1 Anticorps
Cet anticorp ALDH5A1 est non-conjugé
Application
Tous les applications à travers ALDH5A1 Anticorps.
ELISA, Immunohistochemistry (IHC)
Attributs du produit
Polyclonal Antibody
Purification
Affinity purification
Immunogène
Synthetic peptide of human ALDH5A1
Isotype
IgG
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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
0.5 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 ALDH5A1
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Antigène
ALDH5A1
(Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))
Autre désignation
ALDH5A1 (ALDH5A1 Produits )
Synonymes
anticorps SSADH, anticorps SSDH, anticorps Ssadh, anticorps 6330403E24Rik, anticorps Ahd-1, anticorps Ahd1, anticorps D630032B01Rik, anticorps OTTMUSG00000000613, anticorps Ssdh1, anticorps aldehyde dehydrogenase 5 family member A1, anticorps aldehyde dehydrogenase 5 family, member A1, anticorps aldhehyde dehydrogenase family 5, subfamily A1, anticorps ALDH5A1, anticorps aldh5a1, anticorps Aldh5a1
Sujet
This protein belongs to the aldehyde dehydrogenase family of proteins. This gene encodes a mitochondrial NAD(+)-dependent succinic semialdehyde dehydrogenase. A deficiency of this enzyme, known as 4-hydroxybutyricaciduria, is a rare inborn error in the metabolism of the neurotransmitter 4-aminobutyric acid (GABA). In response to the defect, physiologic fluids from patients accumulate GHB, a compound with numerous neuromodulatory properties. Two transcript variants encoding distinct isoforms have been identified for this gene.
NCBI Accession
NP_001071
UniProt
P51649
Pathways
Monocarboxylic Acid Catabolic Process
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