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SLC44A4 Protein (Myc-DYKDDDDK Tag)

SLC44A4 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2732350
  • Target See all SLC44A4 Proteins
    SLC44A4 (Solute Carrier Family 44, Member 4 (SLC44A4))
    Protein Type
    Recombinant
    Origin
    • 3
    • 2
    • 1
    Human
    Source
    • 3
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This SLC44A4 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Solute carrier family 44, member 4 (SLC44A4) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product SLC44A4 Protein
  • 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
    SLC44A4 (Solute Carrier Family 44, Member 4 (SLC44A4))
    Abstract
    SLC44A4 Products
    Synonyms
    zgc:64108 Protein, DKFZp469B0432 Protein, C6orf29 Protein, CTL4 Protein, NG22 Protein, 2210409B01Rik Protein, Ng22 Protein, C7H6orf29 Protein, ctl4 Protein, solute carrier family 44, member 4 Protein, solute carrier family 44 member 4 Protein, solute carrier family 44 member 4 L homeolog Protein, slc44a4 Protein, SLC44A4 Protein, Slc44a4 Protein, slc44a4.L Protein
    Background
    The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene.
    Molecular Weight
    79.1 kDa
    NCBI Accession
    NP_079533
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