ALDH5A1 anticorps (Middle Region)

N° du produit ABIN2788128

Cet anticorps anti-ALDH5A1 est un anticorps Lapin Polyclonal détectant ALDH5A1 dans WB. Adapté pour Humain, Rat, Boeuf (Vache), Lapin et Cobaye.

Aperçu rapide pour ALDH5A1 anticorps (Middle Region) (ABIN2788128)

Antigène: ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))

Reactivité: Humain, Rat, Boeuf (Vache), Lapin, Cobaye

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDH5A1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ALDH5A1 anticorps

Épitope: Middle Region

Séquence: AFFLEWFSEE ARRVYGDIIH TPAKDRRALV LKQPIGVAAV ITPWNFPSAM

Homologie: Cow: 86%, Guinea Pig: 79%, Human: 100%, Rabbit: 79%, Rat: 86%

Attributs du produit: This is a rabbit polyclonal antibody against ALDH5A1. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of human ALDH5A1

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 535 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur ALDH5A1

Antigène: ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))

Autre désignation: 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.
Alias Symbols: SSADH, SSDH
Protein Interaction Partner: MAGEA11, TOMM40, VDAC1, TIAL1, SSBP1, SOD2, EBNA-LP, ABAT,
Protein Size: 535

Poids moléculaire: 57 kDa

ID gène: 7915

NCBI Accession: NM_001080, NP_001071

UniProt: P51649

Pathways: Monocarboxylic Acid Catabolic Process