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CLIP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

This Recombinant CLIP2 protein is expressed in HEK-293 Cells.
Catalog No. ABIN2712880
$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 CLIP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2712880)

Target

See all CLIP2 Proteins
CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))

Protein Type

Recombinant

Origin

  • 2
  • 1
Human

Source

  • 2
  • 1
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Protein Characteristics

    Transcript Variant 1

    Purification tag / Conjugate

    This CLIP2 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human CLIP2 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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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

    CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))

    Alternative Name

    Clip2

    Background

    The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.

    Molecular Weight

    115.6 kDa

    NCBI Accession

    NP_003379

    Pathways

    Microtubule Dynamics
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