Aconitase 1 Phospho-Ser711 (ACO1 pS711) Antibody

Este producto es parte de ACO - Aconitase
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221€ (50 µg)

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935106861
info@markelab.com
name
Aconitase 1 Phospho-Ser711 (ACO1 pS711) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx329919
tested applications
ELISA, WB, IHC

Description

ACO1 (pS711) Antibody is a Rabbit Polyclonal against ACO1 (pS711).

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Aconitase 1 Phospho-Ser711 (ACO1 pS711)
Host
Rabbit
Reactivity
Human, Mouse, Rat, Monkey
Assay Data
Modification: Phosphorylation // Target Modification: Ser711
Recommended Dilution
ELISA: 1/10000, WB: 1/500 - 1/2000, IHC: 1/100 - 1/300. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
50 µg
Size 2
100 µg
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P21399
Gene ID
48
Alias
IRP1,ACONS,HEL60,IREB1,IREBP,IREBP1
Background
Antibody anti-ACO1
Status
RUO

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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