Acetyl-CoA Acetyltransferase 1 (ACAA1) Antibody

Este producto es parte de ACAA - Acetyl Coenzyme A Acyltransferase
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364€ (100 µg)

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935106861
info@markelab.com
name
Acetyl-CoA Acetyltransferase 1 (ACAA1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx230058
tested applications
ELISA, WB, IHC

Description

ACAA1 Antibody is a Rabbit Polyclonal against ACAA1.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Acetyl-CoA Acetyltransferase 1 (ACAA1)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/500 - 1/2000, IHC: 1/50 - 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
P09110
Alias
ACAA, Lnc-Myd88, PTHIO, THIO
Background
Antibody anti-ACAA1
Status
RUO
Note
Concentration: 2 mg/ml - Validity: 12 months.

Descripción

Acetyl Coenzyme A Acyltransferase 1 (ACAA1), also known as thiolase, is a peroxisomal enzyme involved in the final step of beta-oxidation of very-long-chain fatty acids and branched-chain fatty acids. It catalyzes the thiolytic cleavage of 3-ketoacyl-CoA into acetyl-CoA and a shortened acyl-CoA, which is then further metabolized for energy production. ACAA1 is critical for lipid metabolism and plays an important role in energy homeostasis during fasting or periods of high energy demand. Dysregulation of ACAA1 activity can lead to metabolic disorders, such as Zellweger syndrome and other peroxisomal biogenesis disorders, characterized by impaired fatty acid oxidation and accumulation of toxic lipid intermediates. ACAA1 is also being studied for its role in the metabolic reprogramming of cancer cells, where it contributes to lipid catabolism and tumor progression.

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