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兔(CD68)多克隆抗体

  • 货号:FXs39334 可售卖地:全国
  • 品牌:分细生物 保质期:
  • 用途:仅供科研使用 保存温度:避光防潮/2-8℃
  • 价格: ¥1180元 规格:50ul
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分细生物 FXs39334 50ul ¥1180 大量
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Host  :  Rabbit 

Clonality  :   Polyclonal

GeneID   :  12514

Target  :   CD68

Isotype :  IgG

SWISS  :  P31996

Immunogen  :  KLH conjugated synthetic peptide derived from mouse CD68: 111-210/335.<Extracellular >

Purification : affinity purified by Protein A Concentration:1mg/ml

Storage : Preservative:0.02%Proclin300,Constituents:1%BSA,0.01M PBS, pH7.4. Shipped at 4℃.Store at -20℃for one year.Avoid repeated freeze/thaw cycles.

Background :  This gene encodes a 110-kD transmembrane glycoprotein that is highly expressed by human monocytes and tissue macrophages.It is a member of the lysosomal/endosomal-associated membrane 

glycoprotein (LAMP)family.The protein primarily localizes to lysosomes and endosomes with a smaller fraction circulating to the cell surface.It is a type I integral membrane protein with a heavily glycosylated extracellular domain and binds to tissue-and organ-specific lectins or selectins.The protein is also a member of the scavenger receptor family.Scavenger receptors typically function to clear cellular debris,promote phagocytosis,and mediate the recruitment and activation of macrophages. Alternative splicing results in multiple transcripts encoding different isoforms.[provided by RefSeq,Jul 2008]CD68 (Macrosialin)is a 110 kDa integral membrane glycoprotein predominantly expressed on the intracellular lysomsomes of 

monocytes and macrophages and to a lesser extent by dendritic cells and peripheral blood granulocytes.Also,CD68 could play a role in phagocytic activities of tissue macrophages,both in 

intracellular lysosomal metabolism and extracellular cell-cell and cell-pathogen interactions.CD68 is expressed by interdigitating reticulum cells in tonsil and some histiocytic lymphoma or 

histiocytosis,acute myeloid leukemia (AML),and granulocytic sarcoma.Elevated expression of CD68 has been demonstrated on CD34+cells in various human malignancies,including several Acute Myeloid Leukemia studies.