½ðÄê»á¡¤(jinnianhui)½ð×ÖÕÐÅÆ³ÏÐÅÖÁÉÏ-Gold Annual Meeting


  • »¶Ó­À´µ½ÉϺ£Í¨Îµ£¡

    021-54845833/15800441009

    Æ·Öʱ£Ö¤ ¡¤ ͨεÊÔ¼Á

    µ±Ç°Î»ÖÃ: Ê×Ò³ > ¿ÆÑвúÆ· > ¿ÆÑп¹Ìå > Ò»¿¹ > Íÿ¹ARSB¶à¿Ë¡¿¹Ìå

    ²úÆ·ÖÐÐÄ

    ×îвúÆ·

    • Íÿ¹ARSB¶à¿Ë¡¿¹Ìå

      ¹æ¸ñ£º
      ¼Û¸ñ£º£¤
      • Æ·ÅÆ : ͨεÉúÎï
      • Ŀ¼ºÅ : TW2624
      • Ó¦Óà : ½öÓÃÓÚ¿ÆÑÐʹÓÃ
      • »õÆÚ : ÏÖ»õ
      • ¹æ¸ñ £º100ul/200ul/25ul
    • ÉÌÆ·ÏêÇé
    • ²Î¿¼ÎÄÏ×
    • ˵Ã÷ÊéÏÂÔØ
    • ÉÌÆ·ÆÀÂÛ0
    • Ïà¹Ø²úÆ·

    ÖÐÎÄÃû³Æ£º Íÿ¹ARSB¶à¿Ë¡¿¹Ìå   

    Ó¢ÎÄÃû³Æ£º Anti-ARSB rabbit polyclonal antibody

    ±ð      Ãû£º ASB; G4S; MPS6

    Ïà¹ØÀà±ð£º Ò»¿¹

    ´¢      ´æ£º Àä¶³£¨-20¡æ£©

    ËÞ      Ö÷£º Rabbit

    ¿¹      Ô­£º ARSB

    ·´Ó¦ÖÖÊô£º Human

    ±ê ¼Ç Î Unconjugate

    ¿Ë¡ÀàÐÍ£º rabbit polyclonal

    ¼¼Êõ¹æ¸ñ

    Background:

    Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

    Applications:

    ELISA, WB, IHC

    Name of antibody:

    ARSB

    Immunogen:

    Synthetic peptide of human ARSB

    Full name:

    arylsulfatase B

    Synonyms:

    ASB; G4S; MPS6

    SwissProt:

    P15848

    IHC positive control:

    Human gastric cancer and human thyroid cancer

    IHC Recommend dilution:

    50-200

    WB Predicted band size:

    60 kDa

    WB Positive control:

    Human fetal liver tissue

    WB Recommended dilution:

    200-1000







    ¡¾ÍøÕ¾µØÍ¼¡¿¡¾sitemap¡¿


    ¡¾ÍøÕ¾µØÍ¼¡¿¡¾sitemap¡¿