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Arylsulfatase E 抗体

ARSE 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2458596
发货至: 中国
  • 抗原 See all Arylsulfatase E (ARSE) 抗体
    Arylsulfatase E (ARSE)
    适用
    宿主
    • 17
    • 1
    克隆类型
    • 18
    多克隆
    标记
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Arylsulfatase E antibody is un-conjugated
    应用范围
    • 7
    • 7
    • 2
    • 2
    • 2
    • 1
    ELISA, Western Blotting (WB)
    纯化方法
    Antibody is purified by peptide affinity chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ARSE.
    Top Product
    Discover our top product ARSE Primary Antibody
  • 应用备注
    ARSE antibody can be used for detection of ARSE by ELISA at 1:62500. ARSE antibody can be used for detection of ARSE by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    浓度
    1 mg/mL
    缓冲液
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    注意事项
    As with any antibody avoid repeat freeze-thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store ARSE antibody at -20 °C.
  • 抗原
    Arylsulfatase E (ARSE)
    别名
    ARSE (ARSE 产品)
    别名
    ASE antibody, CDPX antibody, CDPX1 antibody, CDPXR antibody, ARSE antibody, MGC155058 antibody, arylsulfatase E (chondrodysplasia punctata 1) antibody, arylsulfatase E antibody, ARSE antibody, Arse antibody
    背景
    Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.
    分子量
    62 kDa
    基因ID
    415
    NCBI登录号
    NP_000038
    UniProt
    P51690
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