Acyl-CoA Synthetase Family Member 2 (ACSF2) Antibody

Este producto es parte de ACSF - Acyl-CoA Synthetase Family Member
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364€ (100 µg)

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935106861
info@markelab.com
name
Acyl-CoA Synthetase Family Member 2 (ACSF2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx230105
tested applications
ELISA, WB, IHC

Description

ACSF2 Antibody is a Rabbit Polyclonal against ACSF2.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Acyl-CoA Synthetase Family Member 2 (ACSF2)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/200 - 1/2000, IHC: 1/20 - 1/200. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purity
≥ 95% (SDS-PAGE)
Purification
Purified by immunogen affinity chromatography.
Size 1
100 µg
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS, pH 7.3, with 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
Q96CM8
Gene ID
80221
OMIM
610465
Alias
ACSMW,AVYV493
Background
Antibody anti-ACSF2
Status
RUO
Note
Concentration: 2 mg/ml - Validity: 12 months.

Descripción

ACSF2 is an acyl-CoA synthetase that plays a pivotal role in the activation of medium-chain fatty acids by converting them into their corresponding acyl-CoA derivatives, facilitating their incorporation into metabolic pathways such as β-oxidation, lipid biosynthesis, and signaling processes. It is predominantly expressed in metabolically active tissues such as the liver and kidney, where it helps maintain energy balance and lipid homeostasis during varying metabolic states. ACSF2 contributes to the formation of bioactive lipids and provides substrates for ATP production, making it integral to intermediary metabolism. Dysregulation of ACSF2 activity has been linked to metabolic disorders, including obesity and fatty acid oxidation deficiencies, where disrupted activation of fatty acids impairs energy production and lipid processing. Its enzymatic specificity underscores its critical role in maintaining cellular metabolic adaptability and systemic lipid regulation.

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