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SLC26A4 Polyclonal Antibody

Catalog Number:

29834
other_names: SLC26A4; DFNB4; EVA; PDS; TDH2B; pendrin

Amount:

100μg
calculated_mw: 86kDa
host_species: Rabbit

Price:

$319

Swiss-Prot No:

Swiss-Prot#:O43511
NCBI Gene ID:5172

Form of Antibody:

Avoid freeze / thaw cycles.|Buffer: PBS with 50% glycerol, pH7.4.

Storage/Stability:

Immunogen:

A synthetic peptide of human SLC26A4 (NP_000432.1).

Purification:

Affinity purification

Specificity/Sensitivity:

Applications:

WB

Background:

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.

References:

appl_detail:

WB 1:500 - 1:2000

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