Alpha-aminoadipic semialdehyde synthase, mitochondrial (AASS) Antibody (FITC)

Este producto es parte de AASS - Alpha-aminoadipic semialdehyde synthase mitochondrial
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169€ (20 µg)

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935106861
info@markelab.com
name
Alpha-aminoadipic semialdehyde synthase, mitochondrial (AASS) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx349269

Description

Alpha-aminoadipic semialdehyde synthase, mitochondrial (AASS) Antibody (FITC) is a Rabbit Polyclonal antibody conjugated to FITC for the detection of Human AASS.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Alpha-aminoadipic semialdehyde synthase, mitochondrial (AASS)
Host
Rabbit
Reactivity
Human
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
FITC
Isotype
IgG
Purity
> 95%
Purification
Purified by Protein G chromatography.
Size 1
20 µg
Size 2
50 µg
Size 3
100 µg
Size 4
200 µg
Size 5
1 mg
Form
Liquid
Buffer
0.01 M PBS, pH 7.4, 0.03% Proclin-300 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
Q9UDR5
Gene ID
10157
NCBI Accession
NM_005763
OMIM
238700
Alias
LKRSDH,LORSDH,LKR/SDH
Background
Antibody anti-AASS
Status
RUO

Descripción

Alpha-aminoadipic semialdehyde synthase (AASS) is a bifunctional mitochondrial enzyme involved in the lysine degradation pathway. It catalyzes two sequential reactions: the oxidation of lysine to saccharopine via its lysine-ketoglutarate reductase activity and the subsequent conversion of saccharopine to alpha-aminoadipic semialdehyde via saccharopine dehydrogenase activity. This pathway plays a crucial role in amino acid catabolism and the production of acetyl-CoA, linking it to energy metabolism and the tricarboxylic acid (TCA) cycle. AASS is essential for maintaining lysine homeostasis and energy production, particularly under conditions of low glucose availability. Mutations in the AASS gene can lead to hyperlysinemia, a metabolic disorder characterized by elevated lysine levels in the blood and associated neurological symptoms. Emerging studies suggest AASS may also play a regulatory role in mitochondrial function and oxidative stress responses.

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