13162017139（微信同号）
13162017139（微信同号）
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.
Pendrin (Sodium-independent chloride/iodide transporter) (Solute carrier family 26 member 4) SLC26A4 PDS
Human
WB;IHC
WB 1:500-2000. IHC 1:20-50.
86kDa
5172
O43511
A synthetic peptide of human SLC26A4
485-535/780aa
Rabbit
Polyclonal
IgG
Cell membrane Secreted
Ion transport #Hearing #Sulfate transport
Affinity purification
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Store at -20℃. Avoid freeze / thaw cycles.
Note: Application as IHC, only suitable for histochemical staining or fluorescence staining of paraffin-embedded sections. Application as ICC/IF, suitable for histochemical or fluorescent staining of frozen sections, as well as chemical and fluorescent staining at the cellular level.
注意：抗体应用为IHC的，抗体只适合于石蜡切片的组化染色或者荧光染色。
抗体应用为IF/ICC的，抗体适合于冰冻切片的组化染色或者荧光染色，以及细胞水平的化学染色和荧光染色。
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应聘职位：hr@ab-mart.com
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销售电话：13162017139（微信同号）
技术支持：15618194176（微信同号）
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