Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (ACADS) Antibody
357.5€ (100 µg)
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Name
Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (ACADS) Antibody
Category
Primary Antibodies
Provider
Abbexa
Reference
abx038041
Tested Applications
ELISA, WB, IHC
Description
Rabbit Polyclonal against the ACADS protein.
Documentos del producto
Instrucciones
Data sheet
Especificaciones del producto
| Category | Primary Antibodies |
| Immunogen Target | Target: Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (ACADS) Immunogen: Recombinant fragment corresponding to 174-397 AA of human ACADS. |
| Host | Rabbit |
| Reactivity | Human |
| Assay Type | Concentration: Lyophilized form: Not applicable. After reconstitution: 1 mg/ml. |
| Recommended Dilution | ELISA: 1/20000 - 1/80000, WB: 1/500 - 1/2000, IHC: 1/100 - 1/200. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | Observed MW: 44 kDa |
| Purification | Purified by Protein A/G column chromatography. |
| Size 1 | 100 µg |
| Size 2 | 1 mg |
| Form | Lyophilized |
| Tested Applications | ELISA, WB, IHC |
| Buffer | Prior to lyophilization: 0.02% NaN3. |
| Availability | Shipped within 7-15 working days. |
| Storage | Store at -20 °C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| Alias | acyl-CoA dehydrogenase C-2 to C-3 short chain,ACAD3,SCAD,Butyryl-CoA Dehydrogenase |
| Background | Antibody anti-ACADS |
| Status | RUO |
| Note | THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION. |
Background
The ACADS gene encodes the enzyme acyl-CoA dehydrogenase short chain, a tetrameric mitochondrial flavoprotein involved in the initial step of the mitochondrial fatty acid beta-oxidation pathway. This enzyme belongs to the acyl-CoA dehydrogenase family and is crucial for metabolizing short-chain fatty acids. Mutations in the ACADS gene have been linked to short-chain acyl-CoA dehydrogenase (SCAD) deficiency, a metabolic disorder. Alternative splicing of this gene produces two variants encoding different isoforms of the enzyme.
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