DFNB31 Antibody (Center) Blocking peptide
€363.00
In stock
SKU
AC-BP11113c
Background:
This gene is thought to function in the organization andstabilization of sterocilia elongation and actin cystoskeletalassembly, based on studies of the related mouse gene. Mutations inthis gene have been associated with autosomal recessivenon-syndromic deafness and Usher Syndrome. Alternative splicing ofthis gene results in multiple transcript variants encodingdifferent isoforms.
Other Names:
Whirlin, Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN
Gene Name: WHRN (HGNC:16361)
Gene ID: 25861
Primary Accession: Q9P202
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene is thought to function in the organization andstabilization of sterocilia elongation and actin cystoskeletalassembly, based on studies of the related mouse gene. Mutations inthis gene have been associated with autosomal recessivenon-syndromic deafness and Usher Syndrome. Alternative splicing ofthis gene results in multiple transcript variants encodingdifferent isoforms.
Other Names:
Whirlin, Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN
Gene Name: WHRN (HGNC:16361)
Gene ID: 25861
Primary Accession: Q9P202
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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