Anti-Ly6g [1A8] antibody (ab210204) is a rat monoclonal antibody that is provided in an azide free formulation. It is used to detect Ly6g in Flow Cytometry, IP, IHC-P, IHC-Fr, FuncS. Suitable for Mouse samples. Available in 5mg, 10mg, 25mg and 50mg sizes for in-vivo use upon request.
- Suitable for in vitro and in vivo studies, including neutralization, blocking, or activation/proliferation
pH: 7.2
Constituents: 0.87% Sodium chloride, 0.12% Sodium dihydrogen phosphate
IP | Flow Cyt | IHC-P | FuncS | IHC-Fr | |
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Mouse | Expected | Expected | Expected | Expected | Expected |
Species | Dilution info | Notes |
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Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
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Lymphocyte antigen 6G, Ly-6G, Ly-6G.1, Ly6g
Anti-Ly6g [1A8] antibody (ab210204) is a rat monoclonal antibody that is provided in an azide free formulation. It is used to detect Ly6g in Flow Cytometry, IP, IHC-P, IHC-Fr, FuncS. Suitable for Mouse samples. Available in 5mg, 10mg, 25mg and 50mg sizes for in-vivo use upon request.
- Suitable for in vitro and in vivo studies, including neutralization, blocking, or activation/proliferation
pH: 7.2
Constituents: 0.87% Sodium chloride, 0.12% Sodium dihydrogen phosphate
ab210204 was purified from tissue culture supernatant via affinity chromatography.
Ly6G also known as lymphocyte antigen 6 complex locus G6D 1A8 or 8C5 is a glycosylphosphatidylinositol (GPI)-anchored cell surface protein. The molecule has a molecular weight of about 25-30 kDa. Its expression is mainly on neutrophils and a subpopulation of eosinophils in mice. It plays a role in the innate immune system marking these immune cells for differentiation and response to infection. Researchers consider it a specific marker for detecting and isolating mouse neutrophils often using methods such as Ly6G staining or anti-Ly6G antibodies for identification.
Ly6G functions in the immune response by facilitating the migration and adhesion of neutrophils to the site of infection or injury. It is part of a protein complex on the cell surface that includes other Ly6 proteins. This group of proteins helps to modulate signal transduction for immune cell functions. Ly6G serves as an anchor through its GPI linkage aiding cell-to-cell communication and signal amplification in inflammation processes.
Ly6G is significantly integrated into the immune signaling pathways notably the toll-like receptor (TLR) signaling pathway. Through these pathways Ly6G influences neutrophil migration and activation. Closely associated proteins include CD11b and CD18 which interact with Ly6G in neutrophil functions including adhesion and transmigration. These pathways are essential for orchestrating the body's defense mechanisms against pathogens.
Ly6G plays an essential role in inflammatory conditions and autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. Aberrant expression or function of Ly6G can alter neutrophil behavior which contributes to disease pathology. Researchers are investigating the relationship between Ly6G and other immune-related proteins like myeloperoxidase (MPO) and elastase as these protein interactions may impact the development and progression of inflammatory diseases.
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We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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Ly6g Flow Cytometry staining of Mouse bone marrow cells using rat Anti-Ly6g antibody
Flow cytometry staining of C57 BL/6 mouse bone marrow cells with ab320706 (right) or Rat IgG2a, kappa monoclonal (Rat IgG2a, kappa monoclonal [RTK2758] - Isotype Control ab18450), isotype control (left). Cells were incubated for 30 min on ice in 1x PBS containing 10% mouse serum and 10 % normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody ab320706 or Rat IgG2a, kappa monoclonal (Rat IgG2a, kappa monoclonal [RTK2758] - Isotype Control ab18450), isotype control (1x 106 in 100 µl at 1.0 μg/ml ) for 30min on ice. The cells were simultaneously stained with APC anti-mouse Ly-6C Antibody.
The secondary antibody Goat Anti-Rat IgG H&L (Alexa Fluor® 488) preadsorbed was incubated at 1/4000 for 30min on ice.
Acquisition of >30000 events were collected using a 50 mW Blue laser (488nm) and 525/40 bandpass filter. Events were gated on live cells.
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