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.
仕様
Synonyms：deafness,autosomal recessive 4,DFNB4,EVA,NSRD4,PDS,Pendred syndrome,Pendred syndrome homolog,Pendrin,S26A4,SLC26A4,Sodium independent chloride/iodide transporter,Sodium-independent chloride/iodide transporter,Solute carrier family 26 member 4
Host：Rabbit
Reactivity：Human
Applications：IHC,ELISA
Concentration：0.5mg/mL
Immunogen：Synthetic peptide of human SLC25A4
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.05％ sodium azide, 50％ glycerol, PH7.3
Dilution：IHC 1：25-1：100
Swissprot：O43511
Isotype：IgG
Research Areas：Cancer, Metabolism, Neuroscience, Signal transduction
