ALDH7A1 antibody

Catalog No. ABIN7264665

Product Details anti-ALDH7A1 Antibody

Target: ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ALDH7A1 antibody is un-conjugated

Application: Immunofluorescence (IF)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Recombinant fusion protein of human ALDH7A1 (NP_001173.2).

Isotype: IgG

Application Details

Application Notes: IF 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for ALDH7A1

Target: ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

Alternative Name: ALDH7A1 (ALDH7A1 Products)

Synonyms: atq1 antibody, ALDH7A1 antibody, ATQ1 antibody, EPD antibody, PDE antibody, antiquitin antibody, ATQ antibody, wu:fi34d12 antibody, wu:fi35e06 antibody, Atq1 antibody, D18Wsu181e antibody, aldehyde dehydrogenase 7 family member A1 antibody, aldehyde dehydrogenase 7 family member A1 L homeolog antibody, aldehyde dehydrogenase 7 family, member A1 antibody, aldehyde dehydrogenase family 7, member A1 antibody, ALDH7A1 antibody, aldh7a1 antibody, aldh7a1.L antibody, Aldh7a1 antibody

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.

Gene ID: 501

UniProt: P49419

Pathways: Sensory Perception of Sound