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The antibody against ACMSD was raised in rabbit using the Fusion protein of Human ACMSD as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
The antibody against ACMSD was raised in rabbit using the Fusion protein of Human ACMSD as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
$299.00
| Cat.No | ADC-31115A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | ACMSD |
| Form | Liquid | Species Reactivity | Human, Mouse |
| Isotype | IgG | Storage Buffer | 0.05% NaN3, 40% Glycerol., pH7.4 PBS |
| Purification Method | Antigen affinity purified | Conjugate | Non-conjugated |
| Application | ELISA, IHC | Storage | Upon receipt |
| Immunogen Description | Fusion protein of Human ACMSD | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | Q8TDX5 |
Uniprot Id
Q8TDX5
Target Species
Human
Target Name
ACMSD
Target Full Name
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
Target Function
Converts alpha-amino-beta-carboxymuconate-epsilon-semialdehyde (ACMS) to alpha-aminomuconate semialdehyde (AMS). ACMS can be converted non-enzymatically to quinolate (QA), a key precursor of NAD, and a potent endogenous excitotoxin of neuronal cells which is implicated in the pathogenesis of various neurodegenerative disorders. In the presence of ACMSD, ACMS is converted to AMS, a benign catabolite. ACMSD ultimately controls the metabolic fate of tryptophan catabolism along the kynurenine pathway.
Target Protein Families
Metallo-dependent hydrolases superfamily, ACMSD family
Target Synonyms
2 amino 3 carboxymuconate 6 semialdehyde decarboxylase; 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase; acmsd; ACMSD_HUMAN; Aminocarboxymuconate semialdehyde decarboxylase; Picolinate carboxylase
Target Background
The neuronal excitotoxin quinolinate is an intermediate in the de novo synthesis pathway of NAD from tryptophan, and has been implicated in the pathogenesis of several neurodegenerative disorders. Quinolinate is derived from alpha-amino-beta-carboxy-muconate-epsilon-semialdehyde (ACMS). ACMSD (ACMS decarboxylase; EC 4.1.1.45) can divert ACMS to a benign catabolite and thus prevent the accumulation of quinolinate from ACMS.
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