Recombinant Human Bartter Syndrome Infantile with Sensorineural Deafness

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POA

SKU:: MBS146293
Additional Names:: [barttin; Barttin; barttin; Bartter syndrome, infantile, with sensorineural deafness (Barttin); deafness, autosomal recessive 73; barttin CLCNK-type chloride channel accessory beta subunit]
Purity:: >90%
Supplier:: MyBiosource
Uniprot:: Q8WZ55
Gene Details:: [BSND]