ALDOA Antikörper (AA 2-364) (HRP)

Produktnummer ABIN1992321

Produktdetails anti-ALDOA Antikörper (HRP)

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

Bindungsspezifität: AA 2-364

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ALDOA Antikörper ist konjugiert mit HRP

Applikation: ELISA

Kreuzreaktivität: Human

Aufreinigung: >95%, Protein G purified

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: ProClin

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

Handhabung: Avoid repeated freeze.
Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

Lagerung: -20 °C,-80 °C

Informationen zur Lagerung: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Details zu ALDOA

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

Andere Bezeichnung: ALDOA (ALDOA Produkte)

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

Hintergrund:

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