SLC26A4 antibody (clone 3D2), anti-human
€435.00
In stock
SKU
AC-AT3915a
Catalog Number: AC-AT3915a
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: E
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Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: E
Request Information AC-AT3915a">Request Information
Background:
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.
Other Names:
Pendrin, Sodium-independent chloride/iodide transporter, Solute carrier family 26 member 4, SLC26A4, PDS
Antigen Type:
Recombinant Protein
Gene Name: SLC26A4
Gene ID: 5172
NCBI Accession: NP_000432.1
Primary Accession: O43511
Other Accession: NM_000441
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.
Other Names:
Pendrin, Sodium-independent chloride/iodide transporter, Solute carrier family 26 member 4, SLC26A4, PDS
Antigen Type:
Recombinant Protein
Gene Name: SLC26A4
Gene ID: 5172
NCBI Accession: NP_000432.1
Primary Accession: O43511
Other Accession: NM_000441
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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