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Invitrogen™ SLC26A4 Polyclonal Antibody
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Catalog No. PIPA5115911
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100 μL
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PIPA5115911 100 μL
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Catalog No. PIPA5115911 Supplier Invitrogen™ Supplier No. PA5115911
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Description

Rabbit Polyclonal Antibody

Antibody detects endogenous levels of total SLC26A4.

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 Western Blot, Immunocytochemistry
Classification Polyclonal
Concentration 1 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.02% sodium azide
Gene SLC26A4
Gene Accession No. O43511, Q9R154, Q9R155
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 A synthesized peptide derived from human SLC26A4(Accession O43511), corresponding to amino acid residues L498-L548.
Purification Method Affinity chromatography
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 23985, 29440, 5172
Target Species Human, Mouse, Rat
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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Safety and Handling

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