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NSJ Bioreagents
SKU:F47643-0.08ML
ACAA1 Antibody
ACAA1 Antibody
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$205.00 USD
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The ACAA1 gene encodes an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of 3-ketoacyl-CoA thiolase (peroxisomal) leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants.
Specifications
| Family | Primary antibody |
|---|---|
| Formulation | In 1X PBS, pH 7.4, with 0.09% sodium azide |
| Format | Antigen affinity purified |
| Host Animal | Rabbit |
| Clonality | Polyclonal (rabbit origin) |
| Isotype | Rabbit Ig |
| Species Reactivity | Human |
| Application | WB, ELISA |
| Application Details | Western blot: 1:1000 |
| Application Note | Titration of the ACAA1 antibody may be required due to differences in protocols and secondary/substrate sensitivity. |
| Immunogen | A portion of amino acids 147-176 from the human protein was used as the immunogen for this ACAA1 antibody. |
| Purity | Antigen affinity |
| Storage | Aliquot the ACAA1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles. |
| Limitation | This ACAA1 antibody is available for research use only. |
| Uniprot # | P09110 |
| Status | Available |
| PDF Link | https://www.nsjbio.com/tds-pdf/acaa1-antibody-f47643 |
| Title | ACAA1 Antibody |
| Description | The ACAA1 gene encodes an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of 3-ketoacyl-CoA thiolase (peroxisomal) leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants. |
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