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ALDH7A1 Protein (Myc-DYKDDDDK Tag)

This Recombinant ALDH7A1 protein is expressed in HEK-293 Cells.
Catalog No. ABIN2714551

Quick Overview for ALDH7A1 Protein (Myc-DYKDDDDK Tag) (ABIN2714551)

Target

See all ALDH7A1 Proteins
ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

Protein Type

Recombinant

Origin

  • 4
  • 2
  • 2
Human

Source

  • 7
  • 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 ALDH7A1 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human ALDH7A1 / ATQ1 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

    ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

    Alternative Name

    Aldh7a1,atq1

    Background

    The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family. These enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular member has homology to a previously described protein from the green garden pea, the 26g pea turgor protein. It is also involved in lysine catabolism that is known to occur in the mitochondrial matrix. Recent reports show that this protein is found both in the cytosol and the mitochondria, and the two forms likely arise from the use of alternative translation initiation sites. An additional variant encoding a different isoform has also been found for this gene. Mutations in this gene are associated with pyridoxine-dependent epilepsy. Several related pseudogenes have also been identified.

    Molecular Weight

    55.2 kDa

    NCBI Accession

    NP_001173

    Pathways

    Sensory Perception of Sound
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