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FMR1 抗体 (AA 1-290)

This anti-FMR1 antibody is a 兔 多克隆 antibody detecting FMR1 in WB, IHC, ELISA, IF 和 IP. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN5697696
发货至: 中国

Quick Overview for FMR1 抗体 (AA 1-290) (ABIN5697696)

抗原

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

适用

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  • 54
  • 42
  • 15
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  • 5
  • 4
  • 4
  • 3
  • 2
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  • 1
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  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 60
  • 21
  • 2

克隆类型

  • 53
  • 30
多克隆

标记

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

应用范围

  • 68
  • 24
  • 20
  • 15
  • 14
  • 14
  • 13
  • 8
  • 8
  • 8
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • 抗原表位

    • 15
    • 8
    • 6
    • 5
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-290

    原理

    FMR1 antibody

    免疫原

    Immunogen sequence: 1-290aa

    Immunogen: fragile X mental retardation 1

    亚型

    IgG
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    说明

    K-562 cells were subjected to SDS PAGE followed by western blot with FNab03172(FMR1 antibody) at dilution of 1:500

    限制

    仅限研究用
  • 缓冲液

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    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.

    注意事项

    Avoid repeated freeze / thaw cycles.

    储存条件

    -20 °C

    储存方法

    -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: Fragile X messenger ribonucleoprotein 1|Fragile X messenger ribonucleoprotein (FMRP)|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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