GRHL2 Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP13148c
Background:
The protein encoded by this gene is a transcription factorthat can act as a homodimer or as a heterodimer with either GRHL1or GRHL3. Defects in this gene are a cause of non-syndromicsensorineural deafness autosomal dominant type 28 (DFNA28).
Other Names:
Grainyhead-like protein 2 homolog, Brother of mammalian grainyhead, Transcription factor CP2-like 3, GRHL2, BOM, TFCP2L3
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP13148c was selected from the Center region of GRHL2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: GRHL2
Gene ID: 79977
Primary Accession: Q6ISB3
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
The protein encoded by this gene is a transcription factorthat can act as a homodimer or as a heterodimer with either GRHL1or GRHL3. Defects in this gene are a cause of non-syndromicsensorineural deafness autosomal dominant type 28 (DFNA28).
Other Names:
Grainyhead-like protein 2 homolog, Brother of mammalian grainyhead, Transcription factor CP2-like 3, GRHL2, BOM, TFCP2L3
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP13148c was selected from the Center region of GRHL2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: GRHL2
Gene ID: 79977
Primary Accession: Q6ISB3
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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