DFNB31 antibody (clone 1D9), anti-human
€435.00
In stock
SKU
AC-AT1757a
Catalog Number: AC-AT1757a
Size: 100 µg
Isotype: mouse IgG2b Kappa
Applications: WB, E
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Size: 100 µg
Isotype: mouse IgG2b Kappa
Applications: WB, E
Request Information AC-AT1757a">Request Information
Background:
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.
Other Names:
Whirlin, Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN
Antigen Type:
Recombinant Protein
Gene Name: WHRN (HGNC:16361)
Gene ID: 25861
NCBI Accession: NP_001077354.2;NP_001166896.1;NP_056219.3
Primary Accession: Q9P202
Other Accession: NM_015404
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.
Other Names:
Whirlin, Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN
Antigen Type:
Recombinant Protein
Gene Name: WHRN (HGNC:16361)
Gene ID: 25861
NCBI Accession: NP_001077354.2;NP_001166896.1;NP_056219.3
Primary Accession: Q9P202
Other Accession: NM_015404
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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