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    • Íÿ¹AMPD1¶à¿Ë¡¿¹Ìå

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    ÖÐÎÄÃû³Æ£º Íÿ¹AMPD1¶à¿Ë¡¿¹Ìå

    Ó¢ÎÄÃû³Æ£º
    Anti-AMPD1 rabbit polyclonal antibody

    ±ð      Ãû£º MAD; MADA

    Ïà¹ØÀà±ð£º Ò»¿¹

    ´¢      ´æ£º Àä¶³£¨-20¡æ£©

    ËÞ      Ö÷£º Rabbit

    ¿¹      Ô­£º
    AMPD1

    ·´Ó¦ÖÖÊô£º Human

    ±ê ¼Ç Î Unconjugate

    ¿Ë¡ÀàÐÍ£º rabbit polyclonal

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    Background:

    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.

    Applications:

    ELISA, WB, IHC

    Name of antibody:

    AMPD1

    Immunogen:

    Synthetic peptide of human AMPD1

    Full name:

    adenosine monophosphate deaminase 1

    Synonyms£º

    MAD; MADA

    SwissProt:

    P23109

    ELISA Recommended dilution:

    2000-10000

    IHC positive control:

    Human liver cancer and Human thyroid cancer

    IHC Recommend dilution:

    100-300

    WB Predicted band size:

    90 kDa

    WB Positive control:

    Human fetal muscle tissue

    WB Recommended dilution:

    500-2000




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