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 > Íÿ¹NSD2¶à¿Ë¡¿¹Ìå

²úÆ·ÖÐÐÄ

×îвúÆ·

  • Íÿ¹NSD2¶à¿Ë¡¿¹Ìå

    ¹æ¸ñ£º
    ¼Û¸ñ£º£¤
    • Æ·ÅÆ : ͨεÉúÎï
    • Ŀ¼ºÅ : TW21045
    • Ó¦Óà : ½ö¹©¿ÆÑÐʹÓÃ
    • »õÆÚ : ÏÖ»õ
    • ¹æ¸ñ £º100ul/200ul/25ul
  • ÉÌÆ·ÏêÇé
  • ²Î¿¼ÎÄÏ×
  • ˵Ã÷ÊéÏÂÔØ
  • ÉÌÆ·ÆÀÂÛ0
  • Ïà¹Ø²úÆ·

ÖÐÎÄÃû³Æ£º Íÿ¹NSD2¶à¿Ë¡¿¹Ìå


Ó¢ÎÄÃû³Æ£º Anti-NSD2 rabbit polyclonal antibody


±ð       Ãû£º nuclear receptor binding SET domain protein 2; WHS


Ïà¹ØÀà±ð£º Ò»¿¹


´¢       ´æ£ºÀä¶³£¨-20¡æ£©


ËÞ       Ö÷£º Rabbit


¿¹      Ô­£º NSD2


·´Ó¦ÖÖÊô£º Human


±ê ¼Ç  Î Unconjugate


¿Ë¡ÀàÐÍ£º rabbit polyclonal


¼¼Êõ¹æ¸ñ

Background:

This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq, Jul 2008]

Applications:

ELISA, IHC

Name of antibody:

NSD2

Immunogen:

Synthetic peptide of human NSD2

Full name:

nuclear receptor binding SET domain protein 2

Synonyms:

WHS; TRX5; KMT3F; KMT3G; MMSET; WHSC1; REIIBP

SwissProt:

O96028

IHC positive control:

Human colorectal cancer

IHC Recommend dilution:

25-100




¡¾ÍøÕ¾µØÍ¼¡¿¡¾sitemap¡¿
¡¾ÍøÕ¾µØÍ¼¡¿¡¾sitemap¡¿