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Complement Factor H 抗体

This anti-Complement Factor H antibody is a 小鼠 单克隆 antibody detecting Complement Factor H in WB, IP, FACS, IHC (p) 和 EIA. Suitable for 人.
产品编号 ABIN492503
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Complement Factor H 抗体 (ABIN492503)

抗原

See all Complement Factor H (CFH) 抗体
Complement Factor H (CFH)

适用

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宿主

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小鼠

克隆类型

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单克隆

标记

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This Complement Factor H antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunoprecipitation (IP), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

克隆位点

OX-24
  • 特异性

    Clone OX-24 inhibits the binding of factor H to surface bound C3. This antibody recognizes the Human serum complement protein factor H and a 43-49 kDa truncated form of factor H.

    交叉反应 (详细)

    Species reactivity (tested):Human.

    产品特性

    Synonyms: CFH, HF, HF1, HF2, H factor 1

    纯化方法

    Protein G Chromatography.

    免疫原

    Purified Human complement factor H protein

    亚型

    IgG1
  • 应用备注

    ELISA. Western blot. Immunoprecipitation. Flow Cytometry. Immunohistochemistry on Paraffin Sections: 20 μg/mL.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    限制

    仅限研究用
  • 浓度

    1.0 mg/mL

    缓冲液

    PBS containing 0.02 % Sodium Azide as preservative.

    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.

    储存条件

    4 °C/-20 °C

    储存方法

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing.
    Shelf life: one year from despatch.

    有效期

    12 months
  • 抗原

    Complement Factor H (CFH)

    背景

    Factor H (CFH) is a protein with twenty short consensus repeat (SCR) domains. Factor H is secreted into the bloodstream and has an essential role in the regulation of complement activation, restricting this innate defense mechanism to microbial infections. Mutations in Factor H have been associated with hemolytic-uremic syndrome (HUS) and chronic hypocomplementemic nephropathy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.Synonyms: CFH, H factor 1, HF, HF1, HF2

    基因ID

    3075

    UniProt

    P08603

    途径

    Complement System, Cellular Response to Molecule of Bacterial Origin
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