Acetyl-CoA Acetyltransferase 1 (ACAA1) Antibody

Este producto es parte de ACAA - Acetyl Coenzyme A Acyltransferase
Acetyl-CoA Acetyltransferase 1 (ACAA1) Antibody
169€ (20 µl)

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Name
Acetyl-CoA Acetyltransferase 1 (ACAA1) Antibody
Category
Primary Antibodies
Provider
Abbexa
Reference
abx322129
Tested Applications
ELISA, WB

Description

ACAA1 Antibody is a Rabbit Polyclonal against ACAA1.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Primary Antibodies
Immunogen Target
Target: Acetyl-CoA Acetyltransferase 1 (ACAA1)
Immunogen: Recombinant human 3-ketoacyl-CoA thiolase, peroxisomal protein (27-300AA).
Host
Rabbit
Reactivity
Human, Mouse
Recommended Dilution
WB: 1/200 - 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Antigen Affinity Chromatography.
Size 1
20 µl
Size 2
50 µl
Size 3
100 µl
Size 4
200 µl
Size 5
1 ml
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.3, containing 0.02% 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
P09110
Gene ID
30
NCBI Accession
NP_001123882.1, NM_001130410.1, NP_001598.1, NM_001607.3
OMIM
604054
Alias
ACAA, Lnc-Myd88, PTHIO, THIO
Background
Antibody anti-ACAA1
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Background

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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