FOXP3 Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP2795c
Background:
FOXP3 is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in FOXP3 gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome.
Other Names:
Forkhead box protein P3, Scurfin, FOXP3, IPEX
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP2795c was selected from the Center region of human FOXP3. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: FOXP3
Gene ID: 50943
Primary Accession: Q9BZS1
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
FOXP3 is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in FOXP3 gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome.
Other Names:
Forkhead box protein P3, Scurfin, FOXP3, IPEX
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP2795c was selected from the Center region of human FOXP3. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: FOXP3
Gene ID: 50943
Primary Accession: Q9BZS1
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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