Human CXCL9/MIG Fluorescein MAb (Clone 49106) 100 TESTS

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Human CXCL9/MIG Fluorescein MAb (Clone 49106) 100 TESTS信息二维码

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产品介绍

    基本参数

    详细说明

    • Species Reactivity

      Human

    • Specificity

      Detects human CXCL9/MIG in ELISAs and Western blots. In ELISAs, does not cross-react with recombinant mouse (rm) CXCL9, recombinant human CXCL10.

    • Source

      Monoclonal Mouse IgG    1 Clone # 49106

    • Purification

      Protein A or G purified from hybridoma culture supernatant

    • Immunogen

      E. coli-derived recombinant human CXCL9/MIG    
      Thr23-Thr125    
      Accession # Q07325

    • Formulation

      Supplied in a saline solution containing BSA and Sodium Azide.

    • Label

      Fluorescein

    Applications

    • Recommended    
      Concentration

      Sample

    • Intracellular Staining by Flow Cytometry

      10 µL/10    6 cells

      See below


    Please Note: Optimal dilutions should be determined by each laboratory for each application.  are available in the Technical Information section on our website.

    Data Examples

    Intracellular Staining by Flow Cytometry      
         

    Detection of CXCL9/MIG in THP‑1 Human Cell Line by Flow Cytometry. THP‑1 human acute monocytic leukemia cell line treated with Recombinant Human IFN‑ gamma (Catalog # ) in the presence of Monensin for 24 hours was stained with Mouse Anti-Human CXCL9/MIG Fluorescein‑conjugated Monoclonal Antibody (Catalog # IC392F, filled histogram) or isotype control antibody (Catalog # , open histogram). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog # ) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog # ). View our protocol for .

    Preparation and Storage

    • Shipping

      The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

    • Stability & Storage

      Protect from light.    Do not freeze.    

      • 12 months from date of receipt, 2 to 8 °C as supplied.

    Background: CXCL9/MIG

    CXCL9, a member of the alpha  subfamily of chemokines that lack the ELR domain, was initially identified as a lymphokine-activated gene in mouse macrophages. Human CXCL9 was subsequently cloned using mouse MIG cDNA as a probe. The CXCL9 gene is induced in macrophages and in primary glial cells of the central nervous system specifically in response to IFN-gamma. CXCL9 has been shown to be a chemoattractant for activated T-lymphocytes and TIL but not for neutrophils or monocytes. The human CXCL9 cDNA encodes a 125 amino acid (aa) residue precursor protein with a 22 aa residue signal peptide that is cleaved to yield a 103 aa residue mature protein. CXCL9 has an extended carboxy-terminus containing greater than 50% basic aa residues and is larger than most other chemokines. The carboxy-terminal residues of CXCL9 are prone to proteolytic cleavage resulting in size heterogeneity of natural and recombinant CXCL9. CXCL9 with large carboxy-terminal deletions have been shown to have diminished activity in the calcium flux assay. A chemokine receptor (CXCR3) specific for CXCL9 and IP-10 has been cloned and shown to be highly expressed in IL-2-activated T-lymphocytes. The E. coli-expressed CXCL9 preparations produced at R&D Systems have been shown to contain greater than 80% full length CXCL9.

    • References:

      1. Loetscher, M. et al. (1996) J. Exp. Med. 184:963.

      2. Liao, F. et al. (1995) J. Exp. Med. 182:1301.

      3. Vanguri, P. (1995) J. Neuroimmunol. 56:35.

    • Entrez Gene IDs:

      4283 (Human); 17329 (Mouse); 246759 (Rat)

    • Alternate Names:

      chemokine (C-X-C motif) ligand 9; CMK; crg-10; C-X-C motif chemokine 9; CXCL9; Gamma-interferon-induced monokine; Humig; MIG; MIGSmall-inducible cytokine B9; monokine induced by gamma interferon; SCYB9Monokine induced by interferon-gamma









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