Acyl-CoA Synthetase Long Chain Family Member 4 (ACSL4) Antibody
325€ (100 µl)
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935106861
info@markelab.com
name
Acyl-CoA Synthetase Long Chain Family Member 4 (ACSL4) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx132816
tested applications
WB, IHC, IF/ICC
Description
Acyl-CoA Synthetase Long Chain Family Member 4 (ACSL4) Antibody is a Rabbit Polyclonal antibody for the detection of Acyl-CoA Synthetase Long Chain Family Member 4 (ACSL4).
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Acyl-CoA Synthetase Long Chain Family Member 4 (ACSL4) |
| Host | Rabbit |
| Reactivity | Rat |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Antigen-specific affinity chromatography followed by Protein A affinity chromatography. |
| Size 1 | 100 µl |
| Size 2 | 200 µl |
| Size 3 | 1 ml |
| Form | Liquid |
| Tested Applications | WB, IHC, IF/ICC |
| Buffer | 0.01 M PBS, pH 7.4, containing 0.05% Proclin-300, 50% glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| Alias | ACS4,FACL4,LACS4 MRX63,MRX68 |
| Background | Antibody anti-ACSL4 |
| Status | RUO |
| Note | Concentration: 0.5 mg/ml - |
Descripción
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Acyl-CoA Synthetase Long Chain Family Member 4 (ACSL4) Antibody
ACSL4 Antibody is a Rabbit Polyclonal antibody against ACSL4. The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates 2 transcript variants.
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