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Invitrogen™ SLC26A4 Polyclonal Antibody
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Catalog No. PIPA598158
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100 μg
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PIPA598158 100 μg
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Catalog No. PIPA598158 Supplier Invitrogen™ Supplier No. PA598158
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Description

Rabbit Polyclonal Antibody

SLC26A4 Polyclonal Antibody for Western Blot, ICC/IF, IHC (P), ELISA

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.
TRUSTED_SUSTAINABILITY

Specifications

Antigen SLC26A4
Applications ELISA, Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry
Classification Polyclonal
Concentration 1 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.03% ProClin 300; pH 7.4
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 Recombinant Human Pendrin protein (592-655AA).
Purification Method Protein G
Quantity 100 μg
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 5172
Target Species Human
Content And Storage -20°C or -80°C if preferred
Product Type Antibody
Form Liquid
Isotype IgG
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