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AMPD1 Protein (Adenosine Monophosphate Deaminase 1) (Myc-DYKDDDDK Tag)

AMPD1 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2714666
$1,112.40
Zzgl. Versandkosten $45.00 und $20.00 Trockeneis
20 μg
Lieferung in 11 Werktagen
  • Target Alle AMPD1 Proteine anzeigen
    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
    Protein-Typ
    Recombinant
    Spezies
    • 2
    • 1
    • 1
    Human
    Quelle
    • 2
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses AMPD1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human AMP deaminase 1 / AMPD1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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
    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
    Andere Bezeichnung
    Amp Deaminase 1,ampd1 (AMPD1 Produkte)
    Synonyme
    ampd1, MAD, MADA, AI553520, Ampd-1, Ampd01, RATAMPD01, zgc:77905, adenosine monophosphate deaminase 1, N-acetyl-anhydromuranmyl-L-alanine amidase, N-acetylmuramoyl-L-alanine amidase, Negative regulator of beta-lactamase expression, adenosine monophosphate deaminase 1 (isoform M), AMPD1, ampD1, ampd1, Ampd1
    Hintergrund
    Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010].
    Molekulargewicht
    90 kDa
    NCBI Accession
    NP_000027
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