Aldehyde Dehydrogenase 18 Family, Member A1 (ALDH18A1) Antibody

Este producto es parte de ALDH - Aldehyde dehydrogenase family member
Aldehyde Dehydrogenase 18 Family, Member A1 (ALDH18A1) Antibody
637€ (100 µl)

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Name
Aldehyde Dehydrogenase 18 Family, Member A1 (ALDH18A1) Antibody
Category
Primary Antibodies
Provider
Abbexa
Reference
abx110914
Tested Applications
ELISA, WB

Description

Aldehyde Dehydrogenase 18 Family, Member A1 Antibody is a Rabbit Polyclonal antibody against Aldehyde Dehydrogenase 18 Family, Member A1.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Primary Antibodies
Immunogen Target
Target: Aldehyde Dehydrogenase 18 Family, Member A1 (ALDH18A1)
Immunogen: Human ALDH18A1.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Antigen Affinity Chromatography.
Size 1
100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.3, containing 0.1% 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
P54886
Gene ID
5832
NCBI Accession
NP_001017423.1, NM_001017423.1, NP_001310341.1, NM_001323412.1, NP_001310342.1, NM_001323413.1
OMIM
138250
Alias
P5CS,Aldehyde dehydrogenase family 18 member A1
Background
Antibody anti-ALDH18A1
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

ALDH18A1, also known as P5CS (pyrroline-5-carboxylate synthase), is a mitochondrial enzyme that catalyzes the conversion of glutamate into pyrroline-5-carboxylate (P5C), a key step in proline and ornithine biosynthesis. This enzyme is crucial for amino acid metabolism, cellular redox balance, and collagen synthesis. ALDH18A1 is highly expressed in tissues with high metabolic activity, such as the liver, kidney, and brain. Mutations in ALDH18A1 are linked to autosomal dominant and recessive forms of P5CS deficiency, which result in hyperammonemia, intellectual disability, and connective tissue disorders due to impaired proline biosynthesis. ALDH18A1 dysfunction also contributes to neurodegenerative diseases and metabolic syndromes by disrupting amino acid metabolism and cellular stress responses. Its role in collagen synthesis makes ALDH18A1 essential for proper skin, bone, and connective tissue maintenance, and it is actively studied for its involvement in aging and fibrosis.

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