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ARSF 抗体 (Cy7)

This anti-ARSF antibody is a 兔 多克隆 antibody detecting ARSF in WB 和 IF (p). Suitable for 人.
产品编号 ABIN1418708
发货至: 中国

Quick Overview for ARSF 抗体 (Cy7) (ABIN1418708)

抗原

See all ARSF 抗体
ARSF (Arylsulfatase F (ARSF))

适用

  • 40
  • 2

宿主

  • 37
  • 3

克隆类型

  • 38
  • 2
多克隆

标记

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This ARSF antibody is conjugated to Cy7

应用范围

  • 33
  • 12
  • 12
  • 8
  • 8
  • 5
  • 5
  • 4
  • 1
  • 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 ARSF

    亚型

    IgG
  • 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

    ARSF (Arylsulfatase F (ARSF))

    别名

    ARSF

    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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