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SLC26A4 Rabbit anti-Human, Polyclonal, Bioss
SDP

Catalog No. 501987496
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50-198-7496 100 μL
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Catalog No. 50-198-7496 Supplier Bioss Supplier No. BS6787R
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Description

Rabbit Polyclonal Antibody

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.

Specifications

Antigen SLC26A4
Applications Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 1 μg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Gene SLC26A4
Gene Accession No. O43511
Gene Alias DFNB4; EVA; PDS; Pendred syndrome homolog; Pendred′s syndrome; Pendrin; SLC26A4; Sodium-independent chloride/iodide transporter; solute carrier family 26 (anion exchanger), member 4; Solute carrier family 26 member 4; solute carrier family 26, member 4; TDH2B; truncated solute carrier family 26
Gene Symbols SLC26A4
Host Species Rabbit
Immunogen KLH conjugated synthetic peptide derived from human Solute carrier family 26 member 4.
Purification Method Protein A
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 5172
Target Species Human
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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