ALDH5A1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA597453-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA597453 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
ALDH5A1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
ALDH5A1
Gene Alias
6330403E24Rik, Ahd1, Ahd-1, aldehyde dehydrogenase 1, mitochondrial, aldehyde dehydrogenase 5 family member A1, aldehyde dehydrogenase 5 family, member A1, aldehyde dehydrogenase 5 family, member A1 (succinate-semialdehyde dehydrogenase), aldehyde dehydrogenase family 5 member A1, aldehyde dehydrogenase family 5, subfamily A1, ALDH5A1, aldhehyde dehydrogenase family 5, subfamily A1, D630032B01Rik, mitochondrial succinate semialdehyde dehydrogenase, NAD(+)-dependent succinic semialdehyde dehydrogenase, OTTMUSG00000000613, SSADH, SSDH, Ssdh1, Succinate-semialdehyde dehydrogenase, mitochondrial, succinic semialdehyde dehydrogenase
Host Species
Rabbit
Purification Method
Protein G
Regulatory Status
RUO
Gene ID (Entrez)
214579, 291133, 7915
Content And Storage
-20°C or -80°C if preferred
Form
Liquid
Applications
ELISA, Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
2.81 mg/mL
Formulation
PBS with 50% glycerol and 0.03% ProClin 300, pH 7.4
Gene Accession No.
P51649, P51650, Q8BWF0
Gene Symbols
ALDH5A1
Immunogen
Recombinant Human Succinate-semialdehyde dehydrogenase, mitochondrial protein (48-535AA)
Quantity
100 μg
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Aldh5A1 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes
- Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation
- Aldh5A1 is a mitochondrial NAD(+)-dependent succinic semialdehyde dehydrogenase
- A deficiency of this enzyme, known as 4-hydroxybutyricaciduria, results in a disorder of the neurotransmitter 4-aminobutyric acid (GABA)
- Symptoms usually include static encephalopathy, associated with developmental delays, hypotonia, ataxia, speech defects, and seizures
- At least two isoforms of Aldh5A1 are known to exist.