SLC26A4 Antibody - Cat. #: CSB-PA192747

SKU: CSB-PA192747

Size :50ul

Clone Number:

Aliases:deafness; autosomal recessive 4 antibody; DFNB4 antibody; EVA antibody; NSRD4 antibody; PDS antibody; Pendred syndrome antibody; Pendred syndrome homolog antibody; Pendrin antibody; S26A4_HUMAN antibody; SLC26A4 antibody; Sodium independent chloride/iodide transporter antibody; Sodium-independent chloride/iodide transporter antibody; Solute carrier family 26 member 4 antibody

Product Type:Polyclonal Antibody

Immunogen Species:Homo sapiens (Human)

UniProt ID:O43511

Immunogen:Synthetic peptide of Human SLC25A4

Raised in:Rabbit

Species Reactivity:Human

Tested Applications:ELISA, IHC; ELISA:1:1000-1:2000, IHC:1:25-1:100

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.

Clonality:Polyclonal

Isotype:IgG

Purification Method:Antigen affinity purification

Conjugate:Non-conjugated

Buffer:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol

Form:Liquid

Stroage:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Target Names:SLC26A4

Research Areas:Neuroscience?Cancer;Metabolism;Signal transduction