Aldehyde Dehydrogenase 3 Family Member A2 (ALDH3A2) Antibody

Este producto es parte de ALDH - Aldehyde dehydrogenase family member
Aldehyde Dehydrogenase 3 Family Member A2 (ALDH3A2) Antibody
455€ (100 µl)

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Name
Aldehyde Dehydrogenase 3 Family Member A2 (ALDH3A2) Antibody
Category
Primary Antibodies
Provider
Abbexa
Reference
abx159324
Tested Applications
ELISA, WB

Description

ALDH3A2 Antibody is a Mouse Monoclonal against ALDH3A2.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Primary Antibodies
Immunogen Target
Target: Aldehyde Dehydrogenase 3 Family Member A2 (ALDH3A2)
Immunogen: Purified recombinant human ALDH3A2 protein fragments expressed in E. coli.
Host
Mouse
Reactivity
Human, Mouse, Rat, Rabbit
Recommended Dilution
WB: 1/500 - 1/5000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Monoclonal
Conjugation
Unconjugated
Isotype
IgG2a
Purification
Purified by affinity chromatography.
Size 1
100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 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
P51648
Alias
ALDH3A2,ALDH10,FALDH
Background
Antibody anti-ALDH3A2
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

ALDH3A2, also known as fatty aldehyde dehydrogenase (FALDH), is a key enzyme that catalyzes the oxidation of fatty aldehydes to fatty acids. This process is essential for lipid metabolism, particularly in the breakdown of long-chain and very-long-chain fatty aldehydes derived from sphingolipids and dietary fats. Mutations in ALDH3A2 cause Sjögren-Larsson Syndrome (SLS), a rare autosomal recessive disorder characterized by ichthyosis (skin scaling), spasticity, and intellectual disability due to the accumulation of fatty aldehydes and disruption of lipid homeostasis. ALDH3A2 is expressed in the liver, brain, and skin, where it supports lipid metabolism and protects against oxidative stress. Its role in maintaining cellular membrane integrity and energy balance highlights its importance in metabolic and neuroprotective functions. Therapies targeting ALDH3A2 aim to restore fatty acid metabolism and alleviate symptoms of SLS, emphasizing its role in lipid-mediated pathologies.

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