SLC26A4 DNAxPab
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Specification
Product Description
Rabbit polyclonal antibody raised against a partial-length human SLC26A4 DNA using DNAx™ Immune technology.
Technology
Immunogen
Extracellular membrane domain (ECD) human DNA
Host
Rabbit
Reactivity
Human
Purification
Protein A
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Immunofluorescence (Transfected cell)
Flow Cytometry (Transfected cell)
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Gene Info — SLC26A4
Entrez GeneID
5172GeneBank Accession#
BC153002Protein Accession#
AAI53003.1Gene Name
SLC26A4
Gene Alias
DFNB4, EVA, PDS
Gene Description
solute carrier family 26, member 4
Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
pendrin
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Interactome
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Disease
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