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ACSL4 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

This Recombinant ACSL4 protein is expressed in HEK-293 Cells.
Catalog No. ABIN2714347

Quick Overview for ACSL4 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2714347)

Target

See all ACSL4 Proteins
ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))

Protein Type

Recombinant

Origin

  • 5
  • 2
  • 1
Human

Source

  • 3
  • 2
  • 1
  • 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 1

    Purification tag / Conjugate

    This ACSL4 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human ACSL4 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Product
    Expression System
    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

    ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))

    Alternative Name

    Acsl4

    Background

    The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants.

    Molecular Weight

    74.3 kDa

    NCBI Accession

    NP_004449
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