Human Cytoplasmic Aconitate Hydratase (ACO1) Protein

Este producto es parte de ACO - Aconitase
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234€ (1 µg)

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935106861
info@markelab.com
name
Human Cytoplasmic Aconitate Hydratase (ACO1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx073951
tested applications
SDS-PAGE

Description

Aconitase-1 is a recombinant enzyme.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Proteins and Peptides
Immunogen Target
Cytoplasmic Aconitate Hydratase (ACO1)
Host
E. coli
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Origin
Human
Observed MW
Concentration: 0.5 mg/ml

Tag: N-terminal His tag
Expression
Recombinant
Purity
> 90% (SDS-PAGE)
Purification
Purified by proprietary chromatographic techniques.
Size 1
1 µg
Size 2
5 µg
Size 3
50 µg
Form
Liquid
Tested Applications
SDS-PAGE
Buffer
20 mM Tris-HCl (pH 8.0), 2 mM DTT, 100 mM NaCl and 10% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Store at 4 °C if entire vial will be used within 2-4 weeks. Store at -20 °C for longer periods of time. For long-term storage, it is recommended to add a carrier protein (0.1% HAS or BSA). Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P21399
Alias
IRP1,ACONS,HEL60,IREB1,IREBP,IREBP1
Background
Protein ACO1
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

Aconitase 1 (ACO1) is a dual-function iron-sulfur protein located in the cytoplasm, acting as both an enzyme and an iron-responsive element-binding protein (IRP1). As an enzyme, ACO1 catalyzes the reversible isomerization of citrate to isocitrate via cis-aconitate in the tricarboxylic acid (TCA) cycle, contributing to cellular energy production. Under low iron conditions, ACO1 switches to its role as IRP1, binding to iron-responsive elements (IREs) in mRNAs to regulate the expression of genes involved in iron metabolism, such as ferritin and transferrin receptor. This functional versatility allows ACO1 to coordinate cellular energy metabolism and iron homeostasis. Dysregulation of ACO1 is implicated in disorders related to iron overload or deficiency, as well as oxidative stress-induced damage in neurodegenerative diseases.

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