3-Ketoacyl-CoA Thiolase, Mitochondrial (ACAA2) Antibody

Este producto es parte de ACAA - Acetyl Coenzyme A Acyltransferase
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637€ (100 µl)

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935106861
info@markelab.com
name
3-Ketoacyl-CoA Thiolase, Mitochondrial (ACAA2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx110749
tested applications
ELISA, WB, IHC

Description

Acetyl-Coenzyme A Acyltransferase 2 Antibody is a Rabbit Polyclonal antibody against Acetyl-Coenzyme A Acyltransferase 2.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
3-Ketoacyl-CoA Thiolase, Mitochondrial (ACAA2)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Antigen Affinity Chromatography.
Size 1
100 µl
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS, pH 7.3, containing 0.1% Sodium Azide and 50% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P42765
Gene ID
10449
OMIM
604770
Alias
DSAEC
Background
Antibody anti-ACAA2
Status
RUO

Descripción

Acetyl Coenzyme A Acyltransferase 2 (ACAA2), also known as mitochondrial 3-ketoacyl-CoA thiolase, is an essential mitochondrial enzyme involved in the beta-oxidation of fatty acids. It catalyzes the thiolytic cleavage of 3-ketoacyl-CoA into acetyl-CoA, which then enters the TCA cycle for ATP production. ACAA2 is highly expressed in energy-demanding tissues such as the liver, heart, and muscle, where it plays a key role in maintaining metabolic flexibility and energy production during fasting or exercise. Mutations or deficiencies in ACAA2 can impair mitochondrial fatty acid oxidation, leading to conditions such as mitochondrial fatty acid oxidation disorders and myopathies. Beyond its metabolic role, ACAA2 activity influences reactive oxygen species (ROS) production and mitochondrial dynamics, linking it to cellular stress responses and metabolic regulation. Ongoing research explores its potential as a therapeutic target for metabolic diseases and mitochondrial dysfunction.

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