
Thermo Fisher Scientific ALDH3A2 Monoclonal Antibody (OTI 1B11), TrueMAB
인간 ALDH3A2 단백질을 인식하는 마우스 단클론 항체로, Western blot에 적합합니다. 동결건조 형태로 제공되며, 재구성 후 약 1 mg/mL 농도로 사용 가능합니다. ALDH3A2 관련 연구 및 단백질 발현 분석에 활용됩니다.
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Applications
- Western Blot (WB): 1:500 dilution tested
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG2b |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI 1B11 |
| Immunogen | Full length human recombinant protein of human ALDH3A2 produced in HEK293T cell |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.3, with 8% trehalose |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
For reconstitution, add 100 µL distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).
Target Information
Aldh3A2 belongs to the aldehyde dehydrogenase superfamily, enzymes that catalyze oxidation of aliphatic and aromatic aldehydes using NAD(P)(+). These enzymes are involved in detoxifying aldehydes from alcohol metabolism and lipid peroxidation.
Aldh3A2 specifically catalyzes oxidation of long-chain aliphatic aldehydes to fatty acids.
Mutations in the ALDH3A2 gene cause Sjogren-Larrson syndrome, a neurocutaneous disorder characterized by ichthyosis, mental retardation, and spastic diplegia, resulting from abnormal lipid accumulation or defective eicosanoid metabolism.
For Research Use Only. Not for use in diagnostic procedures or resale without express authorization.
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