Rat Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1) Protein

Este producto es parte de ALDH - Aldehyde dehydrogenase family member
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208€ (10 µg)

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935106861
info@markelab.com
name
Rat Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx065216
tested applications
WB, SDS-PAGE

Description

Recombinant Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1) is a recombinant Rat protein produced in a Prokaryotic expression system (E. coli).

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryProteins and Peptides
Immunogen TargetAldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1)
HostE. coli
OriginRat
ConjugationUnconjugated
Observed MWMolecular Weight: Calculated MW: 57.0 kDa Concentration: Prior to lyophilization: 200 µg/ml Sequence Fragment: Leu28-Gln539 Tag: N-terminal His tag
ExpressionRecombinant
Purity> 95%
Size 110 µg
Size 250 µg
Size 3100 µg
Size 4200 µg
Size 5500 µg
FormLyophilized To keep the original salt concentration, we recommend reconstituting to the original concentration prior to lyophilization (see Concentration) in ddH2O. If a lower concentration is required, dilute in PBS, pH 7.4. If a higher concentration is required, the product can be reconstituted directly in PBS, pH 7.4, though please note that this will change the overall salt concentration. The stock concentration should be between 0.1-1.0 mg/ml. Do not vortex.
Tested ApplicationsWB, SDS-PAGE
BufferPrior to lyophilization: PBS, pH 7.4, containing 0.01% Sarcosyl, 1 mM DTT, 5% Trehalose and Proclin-300.
AvailabilityShipped within 5-12 working days.
StorageStore at 2-8 °C for up to one month. Store at -80 °C for up to one year. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ64057
AliasALDH7A1,ATQ1
BackgroundProtein ALDH7A1
StatusRUO
NoteThis product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

ALDH7A1, also known as antiquitin, is a multifunctional enzyme involved in lysine catabolism and aldehyde detoxification. It catalyzes the oxidation of α-aminoadipic semialdehyde to α-aminoadipate, a key step in the lysine degradation pathway. Mutations in ALDH7A1 cause pyridoxine-dependent epilepsy (PDE), a rare inherited disorder characterized by seizures that are responsive to vitamin B6 (pyridoxine) supplementation. ALDH7A1 deficiency leads to the accumulation of toxic intermediates, such as α-aminoadipic semialdehyde, which interfere with neurotransmitter function and neuronal health. ALDH7A1 also plays a role in detoxifying aldehydes generated during lipid peroxidation and oxidative stress, protecting tissues from damage. Its expression in the liver, brain, and kidneys highlights its importance in amino acid metabolism, energy production, and cellular defense against aldehyde toxicity.

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