![]() |
||
|---|---|---|
| 【ProductName】 |
SLC26A4 Antibody Blocking Peptide |
|
| 【Cat NO.】 |
K106661P-Ag |
|
| 【Source】 |
Synthetic |
|
| 【Storage】 |
Store at -20℃,2 years.Avoid freeze/thaw cycles. |
|
| 【Appearance】 |
Lyophilized powder |
|
| 【Swiss Prot】 |
O43511 |
|
| 【Gene ID】 |
5172 |
|
| 【Application】 |
Blocking Peptide of K106661P Antibody |
|
| 【Purification】 |
HPLC |
|
| 【Activity】 |
Not tested |
|
| 【Note】 |
Please allow the product to equilibrate to room temperature in a dry environment before opening the packaging. |
|
![]() |
||
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.