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MIγ/CXCL9 Polyclonal Antibody

规格: / 25μL / 100μL
价格: / ¥800 / ¥2100

货号:D-AB-10440L

货期:咨询

宿主: Rabbit

反应性: M,R

应用: WB

  • 详情
  • Overview

    Synonyms C-X-C motif chemokine 9;Gamma-interferon-induced monokine;Monokine induced by interferon-gamma (MIG;MuMIG);Protein m119;Small-inducible cytokine B9;Cxcl9;Mig;Scyb9
    Swissprot P18340
    Source Rabbit
    Reactivity Mouse,Rat
    Immunogen Recombinant Mouse MIγ/CXCL9 protein expressed by E.coli
    Application WB(Detection kit: E-IR-R304)
    Recommended dilution WB,,1:500-1:1000
    Concentration 1mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Nucleus
    Isotype IgG
    Purification Antigen Affinity Purification
    Conjugation Unconjugated
    Storage instructions Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.02% sodium azide,1% BSA and 50% glycerol,pH7.4
    Background Chemokine (C-X-C motif) ligand 9 (CXCL9),also known as Monokine induced by gamma interferon (MIG),is a small cytokine belonging to the CXC chemokine family. The function of this chemokine has not been specifically defined;however,it is thought to be involved in T cell trafficking. CXCL9/MIG functions as one of the three ligands of chemokine receptor CXCR3 which is a G protein-coupled receptor found predominantly on T cells. CXCL9/MIG,together with CXCL10 and CXCL11,may activate CXCR3 by binding to it. CXCL9 serves as a cytokine that affects the growth,movement,or activation state of cells that participate in immune and inflammatory response. It has been observed that tumour endothelial cells secrete high levels of CXCL9 in all,and CXCL10 in most melanoma metastases. Experiment data represent novel mechanisms by which tumour cells in melanoma metastases might use the chemokine-expressing endothelium to leave the tumour and eventually to form additional metastases at distinct sites. Experiment results also improved that CXCL9/MIG plays an important role in CD4+ T lymphocyte recruitment and development of CAV,MOMA-2+ macrophages are the predominant recipient-derived source of CXCL9/MIG,and recipient CD4 lymphocytes are necessary for sustained CXCL9/MIG production and CAV development in this model. Neutralization of the chemokine CXCL9/MIG may have therapeutic potential for the treatment of chronic rejection after heart transplantation.
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