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SLC26A4 Protein (Myc-DYKDDDDK Tag)

SLC26A4 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2732167
发货至: 中国
  • 抗原 See all SLC26A4 蛋白
    SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))
    蛋白类型
    Recombinant
    宿主
    • 5
    • 2
    • 1
    资源
    • 4
    • 2
    • 2
    HEK-293 Cells
    标记
    This SLC26A4 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human SLC26A4 / Pendrin protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product SLC26A4 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))
    别名
    Slc26a4,pendrin (SLC26A4 产品)
    别名
    Pds Protein, DFNB4 Protein, EVA Protein, PDS Protein, TDH2B Protein, pendrin Protein, solute carrier family 26 member 4 Protein, solute carrier family 26, member 4 Protein, SLC26A4 Protein, Slc26a4 Protein
    背景
    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&apos of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.
    分子量
    85.5 kDa
    NCBI登录号
    NP_000432
    途径
    Thyroid Hormone Synthesis, Sensory Perception of Sound
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