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TCF25 抗体 (full length)

The 小鼠 单克隆 anti-TCF25 antibody is suitable to detect TCF25 in samples from 人. It has been validated for WB 和 FACS.
产品编号 ABIN7879167
发货至: 中国
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Room 801-803
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Quick Overview for TCF25 抗体 (full length) (ABIN7879167)

抗原

See all TCF25 抗体
TCF25 (Transcription Factor 25 (Basic Helix-Loop-Helix) (TCF25))

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 TCF25 antibody is un-conjugated

应用范围

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Western Blotting (WB), Flow Cytometry (FACS)

质量等级

Carrier-free

克隆位点

PCRP-TCF25-1A11
  • 抗原表位

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    full length

    原理

    TCF-25 Antibody / Transcription factor 25 (azide and preservative free)

    纯化方法

    Protein A/G affinity

    免疫原

    Recombinant full-length human Transcription factor 25 protein was used as the immunogen for the TCF-25 antibody.

    亚型

    IgG2a
  • 应用备注

    Optimal dilution of the TCF-25 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    -20 °C

    储存方法

    Aliquot the TCF-25 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    TCF25 (Transcription Factor 25 (Basic Helix-Loop-Helix) (TCF25))

    别名

    TCF-25

    背景

    Nulp1 (nuclear localized protein 1), also known as TCF25 (transcription factor 25 (basic helix-loop-helix)), Hulp1 or FKSG26, is a 676 amino acid protein that plays a role in cell death. A member of the TCF25 family, Nulp1 utilizes its C-terminus to mediate transcriptional repression of SRF in vitro, and interacts with XIAP. Nulp1 localizes primarily to the nucleus but is also found in cytosol. Widely expressed, Nulp1 is found at high levels in embryonic brain and adult heart. The gene encoding Nulp1 maps to human chromosome 16q24.3, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn s disease, which is a gastrointestinal inflammatory condition.

    UniProt

    Q9BQ70
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