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TM4SF20 Protein (Myc-DYKDDDDK Tag)

Recombinant TM4SF20 protein expressed in HEK-293 Cells.
Catalog No. ABIN2733827
$956.40
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 TM4SF20 Protein (Myc-DYKDDDDK Tag) (ABIN2733827)

Target

TM4SF20 (Transmembrane 4 L Six Family Member 20 (TM4SF20))

Protein Type

Recombinant

Origin

  • 1
  • 1
Human

Source

  • 2
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

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

    This TM4SF20 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human TM4SF20 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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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

    TM4SF20 (Transmembrane 4 L Six Family Member 20 (TM4SF20))

    Alternative Name

    Tm4sf20

    Background

    The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5.

    Molecular Weight

    24.9 kDa

    NCBI Accession

    NP_079071
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