Aconitate Hydratase, Mitochondrial (ACO2) Antibody

Este producto es parte de ACO - Aconitase
Product Graph
351€ (100 µg)

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935106861
info@markelab.com
name
Aconitate Hydratase, Mitochondrial (ACO2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx375379
tested applications
ELISA, WB

Description

Aconitate Hydratase, Mitochondrial (ACO2) Antibody is a Rabbit Polyclonal antibody against Aconitate Hydratase, Mitochondrial (ACO2).

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Aconitate Hydratase, Mitochondrial (ACO2)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Purification
Purified by affinity chromatography using epitope-specific immunogen.
Size 1
100 µg
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.4, containing 0.02% sodium azide and 50% glycerol.
Availability
Shipped within 5-12 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q99798
Gene ID
50
Alias
ICRD,OCA8,OPA9,ACONM,HEL-S-284
Background
Antibody anti-ACO2
Status
RUO
Note
Concentration: 1 mg/ml -

Descripción

Aconitase 2 (ACO2) is a mitochondrial enzyme involved in the tricarboxylic acid (TCA) cycle, where it catalyzes the reversible isomerization of citrate to isocitrate via cis-aconitate. ACO2 is essential for cellular energy production, linking carbohydrate metabolism to the production of reducing equivalents such as NADH and FADH2. The enzyme contains an iron-sulfur cluster that is critical for its catalytic activity but also makes it sensitive to oxidative damage, which can impair function. Mutations or dysregulation of ACO2 are associated with mitochondrial diseases, neurodegenerative disorders such as Parkinson's disease, and aging, as oxidative stress often leads to loss of aconitase activity. ACO2 is also being explored as a biomarker for mitochondrial dysfunction in metabolic and neurological conditions.

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