Acyl-CoA Dehydrogenase Family Member 9 (ACAD9) Antibody

Este producto es parte de ACAD - Acyl-CoA Dehydrogenase
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169€ (20 µl)

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935106861
info@markelab.com
name
Acyl-CoA Dehydrogenase Family Member 9 (ACAD9) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx321496
tested applications
ELISA, WB, IHC

Description

ACAD9 Antibody is a Rabbit Polyclonal against ACAD9.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Acyl-CoA Dehydrogenase Family Member 9 (ACAD9)
Host
Rabbit
Reactivity
Human
Recommended Dilution
WB: 1/200 - 1/1000, IHC: 1/20 - 1/200. 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, IHC
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
Q9H845
Gene ID
28976
OMIM
611103
Alias
MC1DN20,NPD002
Background
Antibody anti-ACAD9
Status
RUO

Descripción

ACAD9 is a mitochondrial enzyme essential for the β-oxidation of long-chain fatty acids and the assembly of mitochondrial respiratory chain complex I. It functions as a dehydrogenase, catalyzing the first step in the oxidation of long-chain acyl-CoA substrates, generating energy and maintaining lipid homeostasis. ACAD9 is also a critical assembly factor for complex I, facilitating the proper formation and function of this key component of the electron transport chain. Its dual role in fatty acid oxidation and complex I assembly makes ACAD9 indispensable for mitochondrial energy metabolism. Mutations in the ACAD9 gene are associated with complex I deficiency, a severe mitochondrial disorder that can lead to cardiomyopathy, encephalopathy, and metabolic crises. The high expression of ACAD9 in energy-demanding tissues such as the heart, liver, and brain reflects its importance in maintaining mitochondrial function and energy production, positioning it as a vital enzyme in cellular metabolism.

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