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SLC26A4 抗体 (Middle Region)

SLC26A4 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN635614
发货至: 中国
  • 抗原 See all SLC26A4 抗体
    SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))
    抗原表位
    • 16
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    适用
    • 28
    • 16
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 25
    • 3
    克隆类型
    • 26
    • 2
    多克隆
    标记
    • 9
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SLC26A4 antibody is un-conjugated
    应用范围
    • 22
    • 14
    • 13
    • 11
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    特异性
    SLC26 A4 antibody was raised against the middle region of SLC26 4
    纯化方法
    Affinity purified
    免疫原
    SLC26 A4 antibody was raised using the middle region of SLC26 4 corresponding to a region with amino acids ELNDRFRHKIPVPIPIEVIVTIIATAISYGANLEKNYNAGIVKSIPRGFL
    Top Product
    Discover our top product SLC26A4 Primary Antibody
  • 应用备注
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    说明

    SLC26A4 Blocking Peptide, catalog no. 33R-2563, is also available for use as a blocking control in assays to test for specificity of this SLC26A4 antibody

    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of SLC20 4 antibody in PBS
    浓度
    Lot specific
    缓冲液
    PBS
    注意事项
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    储存条件
    4 °C/-20 °C
    储存方法
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • 抗原
    SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))
    别名
    SLC26A4 (SLC26A4 产品)
    别名
    Pds antibody, DFNB4 antibody, EVA antibody, PDS antibody, TDH2B antibody, pendrin antibody, solute carrier family 26 member 4 antibody, solute carrier family 26, member 4 antibody, SLC26A4 antibody, Slc26a4 antibody
    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.
    分子量
    86 kDa (MW of target protein)
    途径
    Thyroid Hormone Synthesis, Sensory Perception of Sound
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