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OCRL Protein (Transcript Variant B) (Myc-DYKDDDDK Tag)

Recombinant OCRL protein expressed in HEK-293 Cells.
Catalog No. ABIN2727866
$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 OCRL Protein (Transcript Variant B) (Myc-DYKDDDDK Tag) (ABIN2727866)

Target

See all OCRL Proteins
OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

Protein Type

Recombinant

Origin

  • 3
  • 1
Human

Source

  • 2
  • 1
  • 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 B

    Purification tag / Conjugate

    This OCRL protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human OCRL (transcript variant b) 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

    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

    Alternative Name

    Ocrl

    Background

    This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants.

    Molecular Weight

    103 kDa

    NCBI Accession

    NP_001578

    Pathways

    Inositol Metabolic Process
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