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ARSF 抗体 (Biotin)

ARSF 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1400839
发货至: 中国
  • 抗原 See all ARSF 抗体
    ARSF (Arylsulfatase F (ARSF))
    适用
    • 43
    • 2
    • 1
    • 1
    宿主
    • 41
    • 2
    克隆类型
    • 42
    • 1
    多克隆
    标记
    • 14
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    This ARSF antibody is conjugated to Biotin
    应用范围
    • 35
    • 17
    • 13
    • 12
    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human ARSF
    亚型
    IgG
    Top Product
    Discover our top product ARSF Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    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 for 12 months.
    有效期
    12 months
  • 抗原
    ARSF (Arylsulfatase F (ARSF))
    别名
    ARSF (ARSF 产品)
    别名
    ASF antibody, ARSF antibody, arylsulfatase F antibody, ARSF antibody
    背景

    Synonyms: Arylsulfatase F, ASF, OTTHUMP00000022857, ARSF_HUMAN.

    Background: Arylsulfatase F, also known as ARSF, is a 590 amino acid secretory protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Arylsulfatase F uses calcium as a cofactor to catalyze reactions that are important in maintaining correct bone composition. The activity of Arylsulfatase F, unlike that of other family members, such as Arylsulfatase E, is not inhibited by warfarin. The gene encoding Arylsulfatase F 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
    416
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