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FMR1 抗体

This anti-FMR1 antibody is a 小鼠 单克隆 antibody detecting FMR1 in WB. Suitable for 人.
产品编号 ABIN5002774
发货至: 中国

Quick Overview for FMR1 抗体 (ABIN5002774)

抗原

See all FMR1 抗体
FMR1 (Fragile X Mental Retardation 1 (FMR1))

适用

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宿主

  • 63
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小鼠

克隆类型

  • 56
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单克隆

标记

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This FMR1 antibody is un-conjugated

应用范围

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Western Blotting (WB)

克隆位点

8C2
  • 交叉反应

    纯化方法

    Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide.

    免疫原

    This FMR1 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 20-48 amino acids from human FMR1.

    亚型

    IgM
  • 应用备注

    WB 1:300-5000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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 for 12 months.

    有效期

    12 months
  • 抗原

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    别名

    FMR1

    背景

    Synonyms: POF, FMRP, POF1, FRAXA, Synaptic functional regulator FMR1, Fragile X mental retardation protein 1, Protein FMR-1, FMR1

    Background: The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene.

    基因ID

    2332

    UniProt

    Q06787

    途径

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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