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CCL7 Protein (AA 24-97)

CCL7 Origin: Mouse Host: Escherichia coli (E. coli) Recombinant > 98 % , as determined by Coomassie stained SDS-PAGE. FACS Active
Catalog No. ABIN2666746
  • Target See all CCL7 Proteins
    CCL7 (Chemokine (C-C Motif) Ligand 7 (CCL7))
    Protein Type
    Recombinant
    Biological Activity
    Active
    Protein Characteristics
    AA 24-97
    Origin
    • 6
    • 4
    • 3
    Mouse
    Source
    • 11
    • 1
    • 1
    Escherichia coli (E. coli)
    Application
    Flow Cytometry (FACS)
    Purity
    > 98 % , as determined by Coomassie stained SDS-PAGE.
    Sterility
    0.22 μm filtered
    Endotoxin Level

    Less than 0.01 ng per μg cytokine as determined by the LAL method.

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    Discover our top product CCL7 Protein
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Comment

    Biological activity: Bioactivity was measured by its property to chemoattract human THP-1 cells in a dose dependent manner.

    Restrictions
    For Research Use only
  • Format
    Liquid
    Reconstitution
    For maximum results, quick spin vial prior to opening. Stock solutions should be prepared at no less than 10 μg/mL in buffer (PBS, DPBS, HBSS, or EBSS) containing carrier protein such as 1 % BSA or HSA or 10 % FBS. After dilution, the cytokine can be stored between 2 °C and 8 °C for one month or from -20 °C to -70 °C for up to 3 months.
    Buffer
    0.22 μm filtered protein solution is in PBS.
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Unopened vial can be stored between 2°C and 8°C for three months, at -20°C for six months, or at -70°C for one year.
  • Target
    CCL7 (Chemokine (C-C Motif) Ligand 7 (CCL7))
    Alternative Name
    CCL7 (CCL7 Products)
    Background
    Mouse CCL7 was initially identified by differential screening of a cDNA library of serum stimulated NIH 3T3 cells. CCL7 has similarity with CCL2/MCP-1 (53 % ) and CCL8/MCP-2 (48 %) at the amino acid level. Chemokines play a key role in inflammation and in the initial phase, CXC chemokines chemoattract polymorpho-nuclear leuckocytes (PMNs). The next step in the inflammatory processes is directed in part by CC chemokines including the monocyte chemoattractant proteins (CCL2, CCL7, CCL8 and CCL13) that chemoattracts additional leucocytes subsets. It has been reported that MMPs regulate chemokine bioactivity, increasing or decreasing their chemoattractant property, MMP-8 and MMP-9 modulate CXC chemokines, and MMP-2 truncates the N-terminal of CCL7 eliminating the first four amino acids producing CCL7(5-76 residues), leading to a loss of activity. The truncated CCL7 binds to its receptor, but it does not induce signaling transduction. MCPs are truncated by different MMPs to create potent antagonists and induce decrease in inflammation. For example, MMP-13 cleaves CCL2 and CCL7 and generates potent receptor antagonists. In an experimental model of myocarditis induced in MMP-2 knockout mice, an increase of CCL7 and high inflammatory response, with pronounced myocardial damage mediated by inflammatory cells, resulted from reduced degradation of CCL7 due to the absence of MMP-2.
    Molecular Weight
    The 74 amino acid recombinant protein has a predicted molecular mass of approximately 10.3 kDa. The DTT-reduced protein migrates at approximately 13 kDa and non-reduced protein migrates at approximately 14.5 kDa by SDS-PAGE. The N-terminal amino acid is G
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