GLYCTK anticorps (AA 251-350) (HRP)

N° du produit ABIN1711352

L’anticorps Lapin Polyclonal anti-GLYCTK a été validé pour WB, ELISA, IHC (p) et IHC (fro). Il convient pour détecter GLYCTK dans des échantillons de Souris.

Aperçu rapide pour GLYCTK anticorps (AA 251-350) (HRP) (ABIN1711352)

Antigène: GLYCTK (Glycerate Kinase (GLYCTK))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GLYCTK est conjugé à/à la HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-GLYCTK anticorps (HRP)

Épitope: AA 251-350

Réactivité croisée: Souris

Homologie: Human,Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human HBEBP2/GLYCTK

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Conseil sur la manipulation: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur GLYCTK

Antigène: GLYCTK (Glycerate Kinase (GLYCTK))

Autre désignation: HBEBP2/GLYCTK

Sujet:

Synonyms: CG9886 like, GLCTK_HUMAN, Glycerate kinase, Glyctk, GLYCTK1, HBeAg binding protein 2, HBeAg binding protein 4, HBeAg-binding protein 4, HBeAgBP4A, HBEBP2, HBEBP4.

Background: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.

ID gène: 132158