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NSJ Bioreagents
SKU:F46753-0.08ML
Anti-FOXP3 Antibody
Anti-FOXP3 Antibody
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Forkhead box P3 is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.
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 |
| Predicted Species Reactivity | Primate |
| Application | WB, ELISA |
| Application Details | Western blot: 1:1000 |
| Application Note | Titration of the anti-FOXP3 antibody may be required due to differences in protocols and secondary/substrate sensitivity. |
| Immunogen | A portion of amino acids 397-423 from the human protein was used as the immunogen for this anti-FOXP3 antibody. |
| Purity | Antigen affinity |
| Storage | Aliquot the anti-FOXP3 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles. |
| Limitation | This anti-FOXP3 antibody is available for research use only. |
| Uniprot # | Q9BZS1 |
| Status | Available |
| PDF Link | https://www.nsjbio.com/tds-pdf/anti-foxp3-antibody-f46753 |
| Title | Anti-FOXP3 Antibody |
| Description | Forkhead box P3 is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. |
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