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ASCL1 Protein (Myc-DYKDDDDK Tag)

This Recombinant ASCL1 protein is expressed in HEK-293 Cells.
Catalog No. ABIN2714974
$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 ASCL1 Protein (Myc-DYKDDDDK Tag) (ABIN2714974)

Target

See all ASCL1 Proteins
ASCL1 (Achaete-Scute Complex Homolog 1 (Drosophila) (ASCL1))

Protein Type

Recombinant

Origin

  • 3
  • 2
  • 1
  • 1
Human

Source

  • 3
  • 2
  • 2
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

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

    This ASCL1 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human ASCL1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Expression System
    Conjugate
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    Expression System Cell-free protein synthesis (CFPS)
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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

    ASCL1 (Achaete-Scute Complex Homolog 1 (Drosophila) (ASCL1))

    Alternative Name

    Ascl1

    Background

    This gene encodes a member of the basic helix-loop-helix (BHLH) family of transcription factors. The protein activates transcription by binding to the E box (5'-CANNTG-3'). Dimerization with other BHLH proteins is required for efficient DNA binding. This protein plays a role in the neuronal commitment and differentiation and in the generation of olfactory and autonomic neurons. Mutations in this gene may contribute to the congenital central hypoventilation syndrome (CCHS) phenotype in rare cases.

    Molecular Weight

    25.3 kDa

    NCBI Accession

    NP_004307

    Pathways

    Dopaminergic Neurogenesis
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