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ATM 抗体 (AA 980-1152)

The 小鼠 单克隆 anti-ATM antibody is suitable to detect ATM in samples from 人. It has been validated for WB, IHC 和 IP.
产品编号 ABIN2469773
发货至: 中国
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北京 101111
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Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for ATM 抗体 (AA 980-1152) (ABIN2469773)

抗原

See all ATM 抗体
ATM (Ataxia Telangiectasia Mutated (ATM))

适用

  • 186
  • 79
  • 34
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  • 1
  • 1

宿主

  • 161
  • 19
  • 5
  • 2
小鼠

克隆类型

  • 122
  • 65
单克隆

标记

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This ATM antibody is un-conjugated

应用范围

  • 111
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Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP)

克隆位点

3-00E-008
  • 抗原表位

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    AA 980-1152

    纯化方法

    Protein G Column

    免疫原

    ATM monoclonal antibody was raised against recombinant protein expressed in E. coli, amino acids 980 - 1512 of ATM (Human).

    亚型

    IgG1
  • 应用备注

    ATM antibody can be used in ELISA starting at 1:200 - 1:1000, Western Blot starting at 1:100 - 1:300, immunocytochemistry starting at 1:75, and immunofluorescence starting at 1:25 - 1:50.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS, pH 7.4. No preservatives added.

    储存液

    Without preservative

    注意事项

    As with all antibodies avoid freeze/thaw cycles.

    储存条件

    -20 °C

    储存方法

    Store ATM antibody at -20 °C.
  • 抗原

    ATM (Ataxia Telangiectasia Mutated (ATM))

    别名

    ATM

    背景

    ATM-3E8 recognizes full-length ATM, a 370 kDa nuclear phosphoprotein, which is involved in the autosomal recessive disease ataxia telangiectasia (AT). ATM belongs to a novel family of proteins associated with cell cycle regulation and response to DNA repair. The C-terminal region has extensive homology to the catalytic domains of phosphatidylinositol 3-kinases (PI3 kinases). Its usefulness to monitor altered ATM expression in cancer is under active investigation. The ATM gene product is a 370 kD nuclear phosphoprotein with C-terminal homology to phosphatidylinositol 3-kinase. ATM is involved in the induction of a DNA damage control pathway. Mutations in the ATM gene cause neuronal degeneration, gonadal abnormalities, and immune deficiencies as part of the hereditary disease ataxia telangiectasia.

    基因ID

    472

    UniProt

    Q13315

    途径

    p53 Pathway, Apoptosis, DNA Damage Repair, Inositol Metabolic Process, Positive Regulation of Response to DNA Damage Stimulus
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