ALDOA anticorps (AA 2-364) (HRP)

N° du produit ABIN1992321

Détail du produit anti-ALDOA anticorps (HRP)

Antigène: ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

Épitope: AA 2-364

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

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

Application: ELISA

Réactivité croisée: Humain

Purification: >95%, Protein G purified

Immunogène: Recombinant Human Fructose-bisphosphate aldolase A protein (2-364AA)

Isotype: IgG

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Preservative: 0.03 % Proclin 300
Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4

Agent conservateur: ProClin

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

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

Stock: -20 °C,-80 °C

Stockage commentaire: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Détails sur ALDOA

Antigène: ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

Autre désignation: ALDOA (ALDOA Produits)

Synonymes: anticorps ALDA, anticorps GSD12, anticorps aldoa, anticorps cb79, anticorps sb:cb79, anticorps wu:fa28b10, anticorps wu:fb10b11, anticorps ALDOA, anticorps Aldo-1, anticorps Aldo1, anticorps RNALDOG5, anticorps hm:zeh0036, anticorps zgc:77696, anticorps aldolase, fructose-bisphosphate A, anticorps aldolase a, fructose-bisphosphate, a, anticorps aldolase, fructose-bisphosphate A S homeolog, anticorps aldolase A, fructose-bisphosphate, anticorps aldolase a, fructose-bisphosphate, b, anticorps ALDOA, anticorps aldoaa, anticorps aldoa, anticorps aldoa.S, anticorps Aldoa, anticorps aldoab

Sujet:

Background: Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein .Defects in ALDOA are the cause of glycogen storage disease type 12 (GSD12) [MIM:611881], also known as red cell aldolase deficiency. A metabolic disorder associated with increased hepatic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis.Belongs to the class I fructose-bisphosphate aldolase family.

Aliases: ALDA antibody, Aldo1 antibody, ALDOA antibody, ALDOA_HUMAN antibody, Aldolase 1 antibody, Aldolase A antibody, Aldolase A fructose bisphosphatase antibody, Aldolase A fructose bisphosphate antibody, Aldolase, fructose-bisphosphate A antibody, Epididymis secretory sperm binding protein Li 87p antibody, FRUCTOALDOLASE A antibody, Fructose 1 6 bisphosphate triosephosphate lyase antibody, Fructose bisphosphate aldolase A antibody, Fructose bisphosphate aldolase antibody, FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE A antibody, Fructose-bisphosphate aldolase A antibody, Fructose-bisphosphate aldolase A Muscle-type antibody, GSD12 antibody, HEL S 87p antibody, Lung cancer antigen NY LU 1 antibody, Lung cancer antigen NY-LU-1 antibody, MGC10942 antibody, MGC17716 antibody, MGC17767 antibody, Muscle type aldolase antibody, Muscle-type aldolase antibody, RNALDOG5 antibody

UniProt: P04075

Pathways: Ribonucleoside Biosynthetic Process