ALDH5A1 (485-496) Goat Polyclonal Antibody
Other products for "ALDH5A1"
Specifications
Product Data | |
Applications | ELISA, IHC, WB |
Recommended Dilution | Peptide ELISA: 1/32000 (Detection Limit). Western blot: 0.3-1 µg/ml. This antibody detects a band of Approx 55kDa in Human Liver lysates and 50kDa band in Mouse and Rat Liver lysates. Immunohistochemistry on Paraffin Sections: 5-10 µg/ml. In paraffin embedded Human Liver shows heavy textured cystoplasm staining in hepatocytes, consistent with mitochondia. |
Reactivities | Bovine, Canine, Human, Mouse, Rat |
Host | Goat |
Clonality | Polyclonal |
Immunogen | Peptide with sequence from the internal region of Human ALDH5A1. |
Specificity | This antibody is expected to recognize both reported isoforms (NP_733936.1; NP_001071.1). |
Formulation | Tris saline, pH~7.3 State: Aff - Purified State: Liquid purified Ig fraction Stabilizer: 0.5% BSA Preservative: 0.02% Sodium Azide |
Concentration | 0.5 mg/ml |
Purification | Ammonium Sulphate Precipitation followed by antigen Affinity Chromatography using the immunizing peptide |
Gene Name | Homo sapiens aldehyde dehydrogenase 5 family member A1 (ALDH5A1), transcript variant 2 |
Database Link | |
Background | Defects in ALDH5A1 are the cause of succinate semialdehyde dehydrogenase deficiency (SSADH deficiency) [MIM:271980]. SSADH deficiency is a rare inborn error in the metabolism of 4-aminobutyric acid (GABA) which leads to accumulation of 4-hydroxybutyric acid in physiologic fluids of patients. The disease is characterized by severe ataxia and by mildly retarded psychomotor development. |
Synonyms | SSADH; SSDH |
Note | Calculated Molecular Weight: 58.7kDa (NP_733936.1). |
Reference Data | |
Protein Families | Druggable Genome |
Protein Pathways | Alanine, aspartate and glutamate metabolism, Butanoate metabolism, Metabolic pathways |
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