ALDOA anticorps (AA 50-364)

N° du produit ABIN7875405

L’anticorps anti-ALDOA Polyclonal Lapin est utilisé pour la détection de ALDOA dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, ELISA, FACS et IHC (p).

Aperçu rapide pour ALDOA anticorps (AA 50-364) (ABIN7875405)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDOA est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-ALDOA anticorps

Épitope: AA 50-364

Fonction: Aldolase A Antibody / ALDOA

Purification: Affinity purified

Immunogène: A human recombinant protein (amino acids E50-Y364) was used as the immunogen for the Aldolase A antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Aldolase A antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the Aldolase A antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur ALDOA

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

Autre désignation: Aldolase A

Sujet: Aldolase A (ALDOA, or ALDA), also known as fructose-bisphosphate aldolase, is an enzyme that in humans is encoded by the ALDOA gene on chromosome 16. This gene encodes a member of the class I fructose-bisphosphate aldolase protein family. The encoded protein is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Mutations in this gene have been associated with Glycogen Storage Disease XII, an autosomal recessive disorder associated with hemolytic anemia. Disruption of this gene also plays a role in the progression of multiple types of cancers. Related pseudogenes have been identified on chromosomes 3 and 10.

UniProt: P04075

Pathways: Ribonucleoside Biosynthetic Process