ALDOA antibody (AA 9-145)

Catalog No. ABIN5611221

The Mouse Monoclonal anti-ALDOA antibody has been validated for WB, ELISA, IHC and FACS. It is suitable to detect ALDOA in samples from Human and Mouse.

Quick Overview for ALDOA antibody (AA 9-145) (ABIN5611221)

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

Reactivity: Human, Mouse

Host: Mouse

Clonality: Monoclonal

Conjugate: This ALDOA antibody is un-conjugated

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

Clone: 1C5B2

Product Details anti-ALDOA Antibody

Binding Specificity: AA 9-145

Purpose: ALDOA Antibody

Purification: Purified antibody

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

Isotype: IgG2a

Application Details

Application Notes:

ELISA: 1/10000

FCM: 1/200 - 1/400

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

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

Storage: 4 °C,-20 °C

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

Target Details for ALDOA

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

Alternative Name: ALDOA

Background: 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.

Molecular Weight: 39.4 kDa

Gene ID: 226

UniProt: P04075

Pathways: Ribonucleoside Biosynthetic Process