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LDLR Protein (Myc-DYKDDDDK Tag)

Recombinant LDLR protein expressed in HEK-293 Cells.
Catalog No. ABIN2724578
$956.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
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Quick Overview for LDLR Protein (Myc-DYKDDDDK Tag) (ABIN2724578)

Target

See all LDLR Proteins
LDLR (Low Density Lipoprotein Receptor (LDLR))

Protein Type

Recombinant

Origin

  • 18
  • 7
  • 3
  • 3
  • 1
Human

Source

  • 18
  • 6
  • 2
  • 2
  • 2
  • 1
  • 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 LDLR protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human LDLR 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

    LDLR (Low Density Lipoprotein Receptor (LDLR))

    Alternative Name

    Ldlr

    Background

    The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. Low density lipoprotein (LDL) is normally bound at the cell membrane and taken into the cell ending up in lysosomes where the protein is degraded and the cholesterol is made available for repression of microsomal enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase, the rate-limiting step in cholesterol synthesis. At the same time, a reciprocal stimulation of cholesterol ester synthesis takes place. Mutations in this gene cause the autosomal dominant disorder, familial hypercholesterolemia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2010].

    Molecular Weight

    93 kDa

    NCBI Accession

    NP_000518

    Pathways

    Hepatitis C, Lipid Metabolism
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