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FMR1 antibody (AA 582-632)

This anti-FMR1 antibody is a Rabbit Polyclonal antibody detecting FMR1 in WB and IP. Suitable for Human and Mouse.
Catalog No. ABIN7450257

Quick Overview for FMR1 antibody (AA 582-632) (ABIN7450257)

Target

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

Reactivity

  • 77
  • 54
  • 44
  • 15
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 62
  • 19
  • 2
Rabbit

Clonality

  • 55
  • 28
Polyclonal

Conjugate

  • 50
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FMR1 antibody is un-conjugated

Application

  • 68
  • 25
  • 23
  • 15
  • 14
  • 13
  • 12
  • 10
  • 9
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Binding Specificity

    • 15
    • 8
    • 6
    • 5
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 582-632

    Purpose

    Rabbit anti-FMR1/FMRP Antibody, Affinity Purified

    Predicted Reactivity

    Orangutan

    Purification

    Affinity Purified

    Immunogen

    Between AA 582 and 632

    Isotype

    IgG
  • Application Notes

    IP: 2 - 10 μg/mg lysate

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

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C

    Expiry Date

    12 months
  • Target

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    Alternative Name

    FMR1/FMRP

    Background

    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).

    Gene ID

    2332

    UniProt

    Q06787, Q86787

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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