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Anti mouse cd117 c kit apc clone 2b8

Manufactured by Thermo Fisher Scientific
Sourced in United States

Anti-mouse CD117 (c-kit) APC (clone 2B8) is a fluorescently-labeled monoclonal antibody that specifically binds to the CD117 (c-kit) antigen expressed on mouse cells. It can be used for the identification and analysis of CD117-positive cells in flow cytometry applications.

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2 protocols using anti mouse cd117 c kit apc clone 2b8

1

Multiparameter Flow Cytometry Analysis

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Anti-mouse CD34 FITC (clone RAM34), anti-mouse CD3 APC (clone145-2C11), anti-mouse CD117 (c-kit) APC (clone 2B8), and anti-mouse Ly-6 A/E (Sca1) CE/Cy7 (clone D7) were purchased from eBioscience (San Diego, CA, USA). Biotin anti-mouse CD4 (clone GK1.5), CE anti-mouse CD4 (clone GK1.5), CE anti-mouse/human CD45R/B220 (clone RA3-6B2), biotin anti-mouse/human CD45R/B220 (clone RA3-6B2), PerCP anti-mouse/human CD45R/B220 (clone RA3-6B2), PerCP anti-mouse/human CD11b (clone M1/70), FITC anti-mouse/human CD11b (clone M1/70), biotin anti-mouse/human CD11b (clone M1/70), PerCP anti-mouse Ly-6G/ Ly-6C(Gr1) (clone RB6-8C5), biotin anti-mouse Ly-6G/ Ly-6C(Gr1) (clone RB6-8C5), CE/Cy7 anti-mouse Ly-6G/Ly-6C(Gr1) (clone RB6-8C5), biotin anti-mouse Ter119 (clone TER119), FITC anti-mouse Ter119 (clone TER119), FITC anti-mouse CD8 (clone 53-6.7), biotin anti-mouse CD8 (clone 53-6.7), CE anti-mouse CD71 (clone RI7217), and PerCP streptavidin were obtained from Biolegend (San Diego, CA, USA). Anti-γH2AX rabbit monoclonal antibody was purchased from Cell Signaling Technology (Danvers, MA, USA). FITC goat anti-rabbit IgG was obtained from ZSGB-BIO Origene (Beijing, China).
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2

Isolation and Characterization of Bone Marrow Cells

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Total BMCs were isolated as described above. Isolated BMCs containing 2 × 106 cells were suspended in 200 μL of staining buffer (2% FBS in PBS), followed by incubation with purified rat anti-mouse CD16/CD32 (Mouse BD Fc Block™; BD Pharmingen) for 10 min at 4 °C. The following fluorescence-conjugated antibodies were then applied and incubated for 30 min at 4 °C: anti-mouse CD140a (PDGFRα APC (clone APA5; BioLegend, San Diego, CA), anti-mouse Lineage Cocktail with Isotype control APC (BD Pharmingen), anti-mouse CD117 (c-kit) APC (clone 2B8; eBioscience), and anti-mouse CD184 (CXCR4) APC (clone 2B11; eBioscience).
As matching isotype controls, fluorescence-conjugated anti-mouse IgG antibodies obtained from either BioLegend or eBioscience were used in each experiment. Stained cells were then analysed on the BD FACSCanto II system. For the sorting experiment, a BD FACSAria II was used. The sorting gates were defined based on the isotype control staining. The FACS data were analysed using FlowJo software, version 6.3.3 (Tree Star, Ashland, OR).
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