- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-LY6C antibody [EPR27220-67] (AB305229)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Tween-20 permeabilized Mouse splenocyte cells labelling LY6C with ab305229 at a 1/100 dilution, followed by Goat Anti-Rabbit (Alexa Fluor® 488) (ab150081) secondary antibody at a 1/1000 dilution. Confocal image showing cytoplasmic staining in subsets of mouse splenocytes (shown in green), which is partially co-located with CD11b. Nuclear DNA was labeled with DAPI (shown in blue).
Counterstained with Anti-CD11b Rat monoclonal antibody (ab8878) at a 1/1000 dilution, followed by Goat Anti-Rat IgG H&L (Alexa Fluor® 594) (ab150160) at a 1/1000 dilution (shown in magenta).
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
The negative controls are as follows :
-ve control 1 : LY6C (ab305229) at a 1/100 dilution, followed by Goat anti-Rat IgG H&L (Alexa Fluor® 594) (ab150160) secondary at a 1/1000 dilution.
-ve control 2 : Anti-CD11b Rat monoclonal antibody (ab8878) at a 1/200 dilution, followed by Goat anti-Rabbit (Alexa Fluor® 488) (ab150081) at a 1/1000 dilution.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-LY6C antibody [EPR27220-67] (AB305229)
Flow cytometric analysis of mouse bone marrow cells labeling Ly6c with ab305229 at 1/500 dilution (0.1ug) (Right panel) compared with a Rabbit monoclonal IgG (ab172730) (Left panel). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody. Cells were stained with rabbit IgG or ab305229, then stained with anti-CD11b conjugated to BV421. Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-LY6C antibody [EPR27220-67] (AB305229)
Flow cytometric analysis of mouse bone marrow cells labeling Ly6c with ab305229 at 1/500 dilution (0.1ug) (Right panel) compared with a Rabbit monoclonal IgG isotype control (ab172730) (Left panel). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody. Cells were stained with rabbit IgG or ab305229. Then stained with anti-B220 conjugated to Alexa Fluor®647. Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-LY6C antibody [EPR27220-67] (AB305229)
Flow cytometric analysis of mouse splenocytes labeling Ly6c with ab305229 at 1/500 dilution (0.1ug) (Right panel) compared with a Rabbit monoclonal IgG isotype control (ab172730) (Left panel). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody. Cells were stained with rabbit IgG or ab305229. Then stained with anti-CD8a conjugated to Alexa Fluor® 647. Gated on viable cells.
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-LY6C antibody [EPR27220-67] - BSA and Azide free
Reactivity 정보
제품 세부 정보
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
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This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Ly6c is involved in the differentiation and trafficking of immune cells. It is not known to be part of a larger protein complex. In the immune system the Ly6c marker is critical for distinguishing between classical and non-classical monocytes in mice. Classical monocytes expressing high levels of Ly6c are involved in rapid response to inflammatory stimuli while non-classical monocytes with lower Ly6c expression help in patrolling blood vessels. This distinction is important in understanding how the immune system responds to various infections and how the body maintains immune homeostasis.
Pathways
Ly6c plays a role in the monocyte recruitment and differentiation pathways. It is closely related to the chemokine signaling pathway influencing how immune cells migrate towards sites of inflammation or injury. The presence of the Ly6c2 protein an isoform of Ly6c helps modulate these responses by interacting with cytokines and chemokines that guide the trafficking of immune cells. The presence of Ly6c influences the activity of proteins like CCR2 which plays a significant role in chemotaxis in response to inflammation.
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