Thermo Fisher Scientific ALDH3A2 Monoclonal Antibody (OTI2A7), TrueMAB
인간 ALDH3A2 단백질을 인식하는 Mouse IgG2b 단일클론 항체로, WB, IHC, Flow Cytometry에 사용 가능. 고순도 Affinity chromatography로 정제되었으며, 안정적인 PBS/BSA/glycerol 버퍼에 보관. 연구용으로만 사용.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:150 |
| Flow Cytometry (Flow) | 1:100 |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG2b |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI2A7 |
| Immunogen | Full length human recombinant protein of human ALDH3A2 produced in HEK293T cells |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.62 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS with 1% BSA, 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Target Information
Aldh3A2 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze oxidation of a wide spectrum of aliphatic and aromatic aldehydes. These enzymes play a major role in detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Aldh3A2 catalyzes oxidation of long-chain aliphatic aldehydes to fatty acids. Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome, an inherited neurocutaneous disorder characterized by ichthyosis, mental retardation, and spastic diplegia. The pathogenesis is associated with abnormal lipid accumulation or defective eicosanoid metabolism.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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