ALDH7A1 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-63890
Catalog Number: E-AB-63890
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: IF
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: IF
Datasheet, Questions? Contact us!
Background:
The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family. These enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular member has homology to a previously described protein from the green garden pea, the 26g pea turgor protein. It is also involved in lysine catabolism that is known to occur in the mitochondrial matrix. Recent reports show that this protein is found both in the cytosol and the mitochondria, and the two forms likely arise from the use of alternative translation initiation sites. An additional variant encoding a different isoform has also been found for this gene. Mutations in this gene are associated with pyridoxine-dependent epilepsy. Several related pseudogenes have also been identified.
Research Area: Cancer, Metabolism, Signal Transduction
Synonyms:
ALDH7A1, ATQ1, EPD, PDE
Immunogen: Recombinant fusion protein of human ALDH7A1 (NP_001173.2).
Swissprot: P49419
Gene ID: 501
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: IF 1:50-1:200
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family. These enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular member has homology to a previously described protein from the green garden pea, the 26g pea turgor protein. It is also involved in lysine catabolism that is known to occur in the mitochondrial matrix. Recent reports show that this protein is found both in the cytosol and the mitochondria, and the two forms likely arise from the use of alternative translation initiation sites. An additional variant encoding a different isoform has also been found for this gene. Mutations in this gene are associated with pyridoxine-dependent epilepsy. Several related pseudogenes have also been identified.
Research Area: Cancer, Metabolism, Signal Transduction
Synonyms:
ALDH7A1, ATQ1, EPD, PDE
Immunogen: Recombinant fusion protein of human ALDH7A1 (NP_001173.2).
Swissprot: P49419
Gene ID: 501
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: IF 1:50-1:200
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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