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S26A4 Polyclonal Antibody

Product Specifications

Background

Solute carrier family 26 member 4 (SLC26A4) Homo sapiens 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, Jul 2008]

Gene ID

5172

Swiss Prot

O43511

Cross Reactivity

Human; Rat; Mouse

Clonality

Polyclonal

Source

Rabbit

Applications

WB; ELISA

Dilution

WB 1:500-2000 ELISA 1:5000-20000

Buffer

Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

Molecular Weight

85

Storage Conditions

-20°C/1 year

Protein Weight

85

Available Sizes

Curated Selection

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