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ROR2 Protein (Myc-DYKDDDDK Tag)

This Recombinant ROR2 protein is expressed in HEK-293 Cells.
Catalog No. ABIN2731087

Quick Overview for ROR2 Protein (Myc-DYKDDDDK Tag) (ABIN2731087)

Target

See all ROR2 Proteins
ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))

Protein Type

Recombinant

Origin

  • 17
  • 4
  • 1
  • 1
Human

Source

  • 13
  • 3
  • 2
  • 2
  • 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 ROR2 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human ROR2 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

    ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))

    Alternative Name

    Ror2

    Background

    The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.

    Molecular Weight

    101.3 kDa

    NCBI Accession

    NP_004551

    Pathways

    RTK Signaling, WNT Signaling
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