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FAM161A Protein (Myc-DYKDDDDK Tag)

FAM161A Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2720762
  • Antigène Voir toutes FAM161A Protéines
    FAM161A (Family with Sequence Similarity 161, Member A (FAM161A))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    • 1
    Humain
    Source
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette FAM161A protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human FAM161A protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product FAM161A Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    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.
    Stock
    -80 °C
    Stockage commentaire
    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.
  • Antigène
    FAM161A (Family with Sequence Similarity 161, Member A (FAM161A))
    Autre désignation
    Fam161a (FAM161A Produits)
    Synonymes
    RP28 Protein, 4930430E16Rik Protein, RGD1304999 Protein, family with sequence similarity 161 member A Protein, family with sequence similarity 161, member A Protein, FAM161A Protein, Fam161a Protein
    Sujet
    This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011].
    Poids moléculaire
    64.7 kDa
    NCBI Accession
    NP_115556
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