S26A4 rabbit pAb
Ref. EK-ES11814
| 50µl | 188.00 € | ||
| 100µl | 316.00 € |
Estimated delivery in United States, on Tuesday 3 Dec 2024
Product Information
Name:
S26A4 rabbit pAb
Description:
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. [provided by RefSeq, Jul 2008],
Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
ELK Biotechnology
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Technical inquiry about: EK-ES11814 S26A4 rabbit pAb
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