Elab Fluor® 647 Anti-Mouse TNFα Antibody[XT3.11]

  • 货号:GFH00567M
Elab Fluor® 647 Anti-Mouse TNFα Antibody[XT3.11]
  • Elab Fluor® 647 Anti-Mouse TNFα Antibody[XT3.11]

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Size:
100 Tests 50 Tests 100 Tests × 2
Alternate Names
Tumor necrosis factor-α, Cachectin, Necrosin, Macrophage cytotoxic factor, Differentiation inducing factor, TNFSF-2, TNF-a, TNF-alpha
Cellular Localization
Secreted
Clone No
Isotype
Rat IgG1, κ
Leadtime
咨询
Background
TNF-α is secreted by macrophages, monocytes, neutrophils, T-cells, and NK-cells. Many transformed cell lines also secrete TNF-α. Monomeric mouse TNF-α is a 156 amino acid protein (N-glycosylated) with a reported molecular weight of 17.5 kD. TNF-α forms multimeric complexes; stable trimers are most common in solution. A 26 kD membrane form of TNF-α has also been described. TNF-α binding to surface receptors elicits a wide array of biologic activities including: cytolysis and cytostasis of many tumor cell lines in vitro, hemorrhagic necrosis of tumors in vivo, increased fibroblast proliferation, and enhanced chemotaxis and phagocytosis in neutrophils.
Abbre
TNF-α
Swissprot
Host
Rat
Reactivity
Mouse
Clonality
Monoclonal
Isotype Control
Elab Fluor® 647 Rat IgG1, κ Isotype Control[HRPN]
Applications
ICFCM
Form
Liquid
Concentration
5 μL/Test
Conjugation
Elab Fluor®647
Conjugation Information
Elab Fluor® 647 is designed to be excited by the Red laser (627-640 nm) and detected using an optical filter centered near 670 nm (e.g., a 660/20 nm bandpass filter).
Spectrum
Storage Buffer
Phosphate buffered solution, pH 7.2, containing 0.09% sodium azide and 1% BSA.
Storage
This product can be stored at 2-8°C for 12 months. Please protected from prolonged exposure to light and do not freeze.
Expiration Date
12个月
Shipping
冰袋
Gene ID
Mouse splenocytes were stimulated with Cell Stimulation MIX and Protein Transport Inhibitor MIX for 5 hours.Cells were stained with FITC Anti-Mouse CD4 Antibody and Elab Fluor® 647 Rat IgG1,κ Isotype Control (left) or Elab Fluor® 647 Anti-Mouse TNF-α[XT3.11] (right). Cells in the lymphocytes gate were used for analysis.
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