ALDH6A1 anticorps (AA 326-535)

N° du produit ABIN6136780

Cet anticorps Lapin Polyclonal détecte spécifiquement ALDH6A1 dans WB et IF. Il présente une réactivité envers Humain.

Aperçu rapide pour ALDH6A1 anticorps (AA 326-535) (ABIN6136780)

Antigène: ALDH6A1 (Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDH6A1 est non-conjugé

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

Détail du produit anti-ALDH6A1 anticorps

Épitope: AA 326-535

Séquence: VGEAKKWLPE LVEHAKNLRV NAGDQPGADL GPLITPQAKE RVCNLIDSGT KEGASILLDG RKIKVKGYEN GNFVGPTIIS NVKPNMTCYK EEIFGPVLVV LETETLDEAI QIVNNNPYGN GTAIFTTNGA TARKYAHLVD VGQVGVNVPI PVPLPMFSFT GSRSSFRGDT NFYGKQGIQF YTQLKTITSQ WKEEDATLSS PAVVMPTMGR

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 326-535 of human ALDH6A1 (NP_005580.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IF,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 ALDH6A1

Antigène: ALDH6A1 (Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))

Autre désignation: ALDH6A1

Sujet: This gene encodes a member of the aldehyde dehydrogenase protein family. The encoded protein is a mitochondrial methylmalonate semialdehyde dehydrogenase that plays a role in the valine and pyrimidine catabolic pathways. This protein catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids. Alternate splicing results in multiple transcript variants.,ALDH6A1,MMSADHA,MMSDH,Epigenetics & Nuclear Signaling,RNA Binding,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Amino acid metabolism,ALDH6A1

Poids moléculaire: 56 kDa/57 kDa

ID gène: 4329

UniProt: Q02252

Pathways: Brown Fat Cell Differentiation