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Arylsulfatase H 抗体 (AbBy Fluor® 555)

ARSH 适用: 人 WB, IF (p) 宿主: 兔 Polyclonal AbBy Fluor® 555
产品编号 ABIN1400843
发货至: 中国
  • 抗原 See all Arylsulfatase H (ARSH) 抗体
    Arylsulfatase H (ARSH)
    适用
    • 32
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    宿主
    • 29
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    克隆类型
    • 32
    多克隆
    标记
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    This Arylsulfatase H antibody is conjugated to AbBy Fluor® 555
    应用范围
    • 21
    • 12
    • 7
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human ARSH
    亚型
    IgG
    Top Product
    Discover our top product ARSH Primary Antibody
  • 应用备注
    IF(IHC-P) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    Arylsulfatase H (ARSH)
    别名
    ARSH (ARSH 产品)
    别名
    ARSH antibody, LOC100232370 antibody, sulfatase antibody, arylsulfatase family member H antibody, arylsulfatase D antibody, ARSH antibody, LOC100232370 antibody, LOC100229427 antibody
    背景

    Synonyms: Arylsulfatase H, ASH, ARSH_HUMAN.

    Background: Sulfatases hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling and degradation of macromolecules. Arylsulfatase H, also known as ARSH, is a 562 amino acid protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Localized to the plasma membrane, Arylsulfatase H uses calcium as a cofactor to hydrolyze sulfate esters. The gene encoding Arylsulfatase D maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.

    基因ID
    347527
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