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Arylsulfatase E 抗体 (Middle Region)

The 兔 多克隆 anti-Arylsulfatase E antibody is suitable to detect Arylsulfatase E in samples from 人. It has been validated for WB.
产品编号 ABIN2776926
发货至: 中国
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Quick Overview for Arylsulfatase E 抗体 (Middle Region) (ABIN2776926)

抗原

See all Arylsulfatase E (ARSE) 抗体
Arylsulfatase E (ARSE)

适用

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宿主

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克隆类型

  • 19
多克隆

标记

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This Arylsulfatase E antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    Middle Region

    序列

    KVVHHDPPLL FDLSRDPSET HILTPASEPV FYQVMERVQQ AVWEHQRTLS

    预测反应

    Human: 100%

    产品特性

    This is a rabbit polyclonal antibody against ARSE. It was validated on Western Blot using a cell lysate as a positive control.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the middle region of human ARSE
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 589 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    Arylsulfatase E (ARSE)

    别名

    ARSE

    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. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-170 AC005295.1 87561-87730 c 171-744 AK223183.1 1-574 745-2036 AK223199.1 542-1833 2037-2220 AW779826.1 1-184 c
    Alias Symbols: CDPX, CDPX1, CDPXR, MGC163310, ASE
    Protein Interaction Partner: COQ6, TMEM259, TNK2, NDN,
    Protein Size: 589

    分子量

    62 kDa

    基因ID

    415

    NCBI登录号

    NM_000047, NP_000038

    UniProt

    P51690
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