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PLCE1 Protein (Myc-DYKDDDDK Tag)

This Recombinant PLCE1 protein is produced in HEK-293 Cells.
Catalog No. ABIN2729133
$1,112.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
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Quick Overview for PLCE1 Protein (Myc-DYKDDDDK Tag) (ABIN2729133)

Target

See all PLCE1 Proteins
PLCE1 (Phospholipase C, epsilon 1 (PLCE1))

Protein Type

Recombinant

Origin

  • 1
  • 1
  • 1
Human

Source

  • 3
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Purification tag / Conjugate

    This PLCE1 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human PLCE1 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

    PLCE1 (Phospholipase C, epsilon 1 (PLCE1))

    Alternative Name

    Plce1

    Background

    This gene encodes a phospholipase enzyme that catalyzes the hydrolysis of phosphatidylinositol-4,5-bisphosphate to generate two second messengers: inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). These second messengers subsequently regulate various processes affecting cell growth, differentiation, and gene expression. This enzyme is regulated by small monomeric GTPases of the Ras and Rho families and by heterotrimeric G proteins. In addition to its phospholipase C catalytic activity, this enzyme has an N-terminal domain with guanine nucleotide exchange (GEF) activity. Mutations in this gene cause early-onset nephrotic syndrome characterized by proteinuria, edema, and diffuse mesangial sclerosis or focal and segmental glomerulosclerosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]

    Molecular Weight

    258.5 kDa

    NCBI Accession

    NP_057425

    Pathways

    EGFR Signaling Pathway, Regulation of G-Protein Coupled Receptor Protein Signaling
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