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A2BP1 抗体 (N-Term)

This anti-A2BP1 antibody is a 小鼠 单克隆 antibody detecting A2BP1 in WB, ICC 和 IF. Suitable for 人, 小鼠, 大鼠 和 Cow.
产品编号 ABIN1951829
发货至: 中国

Quick Overview for A2BP1 抗体 (N-Term) (ABIN1951829)

抗原

See all A2BP1 抗体
A2BP1 (Ataxin 2-Binding Protein 1 (A2BP1))

适用

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人, 小鼠, 大鼠, Cow

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 A2BP1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • 抗原表位

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    AA 1-100, N-Term

    特异性

    Immunostaining Cell Cultures
    1. Draw of culture medium with aspirator and add 1 ml of 3.7 % formalin in PBS solution to the dish. (make up from 10mls
    Fisher 37% formalin plus 90mls PBS, the Fisher formalin contains 37% formaldehyde plus about 1% methanol which may be
    relevant sometimes). Let sit at room temp for 1 minute. (can add 0.1% Tween 20 to PBS used here and all subsequent steps
    to reduce background, probably best not to do this first time round though as it may extract your antigen or help wash your
    cells off the dish).
    2. Take off the formalin/PBS and add 1ml of cold methanol (-20°C, kept in well sealed bottle in fridge). Let sit for no more
    than 1 minute.
    3. Take off methanol and add 1ml of PBS, not letting the specimen dry out. To block nonspecific antibody binding can add
    ~10ml (=1%) of goat serum (Sigma), and can incubate for 30 minutes. Can then add antibody reagents. Typically 100ml of
    hybridoma tissue culture supernatent or 1ml of mouse ascites fluid or crude serum. Incubate for 1 hour at room temp. (or
    can go at 37°C for 30 minutes to 1 hour, or can do 4°C overnight, exact time not too critical). Can do very gentle shaking for
    well adherent cell lines (3T3, Hek293 etc.).
    4. Remove primary antibody and replace with 1 ml of PBS. Let sit for 5-10 minutes, replace PBS and repeat twice, to give
    three washes in PBS.
    5. Add 0.5 mls of secondary antibody. These are fluorescently labeled Goat anti mouse antibodies and are conjugated to
    ALEXA dyes and are from Molecular probes (Eugene Oregon, the ALEXA dyes are sulphonated rhodamine compounds and
    are much more stable to UV than FITC, TRITC, Texas red etc.). Typically make 1:2,000 dilutions of these secondaries in
    PBS plus 1% goat serum, BSA or non fat milk carrier. Incubate for 1 hour at room temp. (or can go at 37°C for 30 minutes to
    1 hour, or can do 4°C overnight). Can do gentle shaking for well adherent cell lines (3T3, HEK293 etc.).
    6. Remove secondary antibody and replace with 1 ml of PBS. Let sit for 5-10 minutes, replace PBS and repeat twice, to give
    three washes in PBS.
    7. Drop on one drop of Fisher mounting medium onto dish and apply 22mm square coverslip. View in the microscope!




    Immunostaining Tissue

    纯化方法

    Aff - Purified

    免疫原

    Purified human recombinant protein fragment structure from E. Coli. corresponding to N terminal AA 1-100 of Human FOX1

    亚型

    IgG1
  • 应用备注

    Immunofluorescence: 1:1:500-1:1,000 , Western Blot: 1:1,000-1:2,000, Dilutions listed as a recommendation. Optimal dilution should be determined by investigator.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.0 mg/mL

    缓冲液

    Purified tissue culture supernatant in PBS with 10mM sodium azide preservative.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    4 °C

    储存方法

    Antibody can also be aliquotted and stored frozen at -20° C to -70° C in a manual defrost , freezer for six months without detectable loss of activity. The antibody can be stored at 2° - 8°C for 1 month without detectable loss of activity.
  • 抗原

    A2BP1 (Ataxin 2-Binding Protein 1 (A2BP1))

    别名

    FOX1 / A2BP1
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