ALDOA Antikörper (AA 9-145)

Produktnummer ABIN5611221

Produktdetails anti-ALDOA Antikörper

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

Bindungsspezifität: AA 9-145

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser ALDOA Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)

Verwendungszweck: ALDOA Antibody

Aufreinigung: Purified antibody

Immunogen: Purified recombinant fragment of human ALDOA (AA: 9-145) expressed in E. Coli.

Klon: 1C5B2

Isotyp: IgG2a

Anwendungsinformationen

Applikationshinweise:

ELISA: 1/10000

FCM: 1/200 - 1/400

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified antibody in PBS with 0.05 % sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

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:

Description: The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), 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. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10.

Aliases: ALDA, GSD12, HEL-S-87p

Molekulargewicht: 39.4kDa

Gen-ID: 226

HGNC: 226

UniProt: P04075

Pathways: Ribonucleoside Biosynthetic Process