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FMR1 Protein (Myc-DYKDDDDK Tag)

This Recombinant FMR1 protein is expressed in HEK-293 Cells.
Catalog No. ABIN2721259
$1,112.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
Shipping to: United States
Delivery in 11 to 12 Business Days

Quick Overview for FMR1 Protein (Myc-DYKDDDDK Tag) (ABIN2721259)

Target

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

Protein Type

Recombinant

Origin

  • 6
  • 1
  • 1
Human

Source

  • 2
  • 2
  • 2
  • 1
  • 1
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Purification tag / Conjugate

    This FMR1 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human FMR1 / FMRP protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Expression System
    Conjugate
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    Expression System Cell-free protein synthesis (CFPS)
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    Origin Human
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  • Application Notes

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Comment

    The tag is located at the C-terminal.

    Restrictions

    For Research Use only
  • Concentration

    50 μg/mL

    Buffer

    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

    Storage

    -80 °C

    Storage Comment

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

    FMR1 (Fragile X Mental Retardation 1 (FMR1))

    Alternative Name

    Fmr1,fmrp

    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.

    Molecular Weight

    71 kDa

    NCBI Accession

    NP_002015

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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