SLC26A4 Polyclonal Antibody

Rs. 16,500.00
SKU E-AB-16833


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
Swissprot O43511
Source Rabbit
Reactivity Human
Immunogen Synthetic peptide of human SLC25A4
Application IHC,ELISA
Recommended dilution IHC 1:25-1:100
Concentration 0.6mg/mL
Clonality Polyclonal


Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
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.


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