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FMR1 抗体 (AA 36-279)

The 小鼠 单克隆 anti-FMR1 antibody (Clone 1D10) (ABIN2721254) specifically detects FMR1 in WB 和 IHC. The antibody is reactive with 人, 小鼠, 大鼠, 犬 和 猴 samples.
产品编号 ABIN2721254
发货至: 中国
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Quick Overview for FMR1 抗体 (AA 36-279) (ABIN2721254)

抗原

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

适用

  • 95
  • 73
  • 61
  • 15
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
人, 小鼠, 大鼠, 犬, 猴

宿主

  • 78
  • 20
  • 2
小鼠

克隆类型

  • 53
  • 47
单克隆

标记

  • 46
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FMR1 antibody is un-conjugated

应用范围

  • 85
  • 37
  • 32
  • 25
  • 16
  • 15
  • 14
  • 13
  • 8
  • 8
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)

克隆位点

1D10
  • 抗原表位

    • 15
    • 8
    • 6
    • 5
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 36-279

    产品特性

    Homo sapiens fragile X mental retardation 1 (FMR1), transcript variant ISO1

    纯化方法

    Purified from mouse ascites fluids by affinity chromatography

    免疫原

    Human recombinant protein fragment corresponding to amino acids 36-279 of human FMR1(NP_002015) produced in E.coli.

    亚型

    IgG2b
  • 应用备注

    WB 1:500~2000, IHC 1:50,

    说明

    The concentration of the product may vary between diferrent lots.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5-1.0 mg/mL

    缓冲液

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

    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

    -20 °C
  • 抗原

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    别名

    FMR1

    背景

    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.

    分子量

    71 kDa

    基因ID

    2332

    NCBI登录号

    NM_002024

    HGNC

    2332

    途径

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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