Solarbio

SLC26A4 Antibody Blocking Peptide

توضیحات و پروتکل‌های فنی

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.

مشخصات و اطلاعات آزمایشگاهی

کد کاتالوگ:

C-K106661P-Ag-500ug

وضعیت تامین:

موجود در انبار سیترا بیوتک

Appearance:

Lyophilized powder

Storage:

Store at -20℃ 2 years.Avoid freeze/thaw cycles.

Unit:

Piece

Source:

Synthetic

تحویل:

یک ماه پس از سفارش

انتخاب مقیاس / حجم بسته‌بندی:

500ug

46800000 تومان