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RIN2 Protein (Myc-DYKDDDDK Tag)

Recombinant RIN2 protein expressed in HEK-293 Cells.
Catalog No. ABIN2730929

Quick Overview for RIN2 Protein (Myc-DYKDDDDK Tag) (ABIN2730929)

Target

See all RIN2 Proteins
RIN2 (Ras and Rab Interactor 2 (RIN2))

Protein Type

Recombinant

Origin

  • 3
  • 2
Human

Source

  • 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 RIN2 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human RIN2 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Product
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    Conjugate
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    Expression System HEK-293 Cells
    Conjugate His tag
    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

    RIN2 (Ras and Rab Interactor 2 (RIN2))

    Alternative Name

    Rin2

    Background

    The RAB5 protein is a small GTPase involved in membrane trafficking in the early endocytic pathway. The protein encoded by this gene binds the GTP-bound form of the RAB5 protein preferentially over the GDP-bound form, and functions as a guanine nucleotide exchange factor for RAB5. The encoded protein is found primarily as a tetramer in the cytoplasm and does not bind other members of the RAB family. Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants.

    Molecular Weight

    100 kDa

    NCBI Accession

    NP_061866
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