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FMR1 抗体 (AA 600-650)

The 兔 多克隆 anti-FMR1 antibody is suitable to detect FMR1 in samples from 人 和 小鼠. It has been validated for WB 和 IP.
产品编号 ABIN7450256
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for FMR1 抗体 (AA 600-650) (ABIN7450256)

抗原

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

适用

  • 94
  • 72
  • 61
  • 15
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
人, 小鼠

宿主

  • 77
  • 20
  • 2

克隆类型

  • 52
  • 47
多克隆

标记

  • 45
  • 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

  • 84
  • 37
  • 33
  • 25
  • 16
  • 15
  • 14
  • 13
  • 8
  • 7
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • 抗原表位

    • 15
    • 8
    • 6
    • 5
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 600-650

    原理

    Rabbit anti-FMR1/FMRP Antibody, Affinity Purified

    预测反应

    Rat

    纯化方法

    Affinity Purified

    免疫原

    Between AA 600 and 650

    亚型

    IgG
  • 应用备注

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    限制

    仅限研究用
  • 浓度

    1000 μg/mL

    缓冲液

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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

    4 °C

    有效期

    12 months
  • 抗原

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    别名

    FMR1/FMRP

    背景

    Background: Fragile X mental retardation protein 1 is the product of the gene FMR1, also known as FMRP. This protein binds RNA and is associated with polysomes. FMRP may also 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).

    基因ID

    2332

    UniProt

    Q06787, Q86787

    途径

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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