| 货号 | MCA1218F |
| 克隆号 | MIL2 |
| 同种亚型 | IgG2b |
| 反应种属 | Pig |
| 来源宿主 | Mouse |
| 应用 | F |
| 供应商 | Bio-Rad Antibodies |
| 运输条件 | |
| 存放说明 | Store at +4oC or at -20oC if preferred. Storage in frost-free freezers is not recommended. This product should be stored undiluted. This product is photosensitive and should be protected from light. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.Store at +4oC or at -20oC if preferred. This product should be stored undiluted. Storage in frost-free freezers is not recommended. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use. |
| 本官网所有报价均为常温或者蓝冰运输价格，如有产品需要干冰运输，需另外加收干冰运输费。 |
Staining of pig peripheral blood granulocytes with Mouse anti Pig CD14 (MCA1218GA) followed by Goat anti Mouse IgG:FITC (STAR117F) | |
Published customer image: Mouse anti Pig CD14 antibody, clone MIL2 used for the evaluation of CD14 expression on porcine leukocytes by flow cytometry. Image caption: Overview of flow cytometry analyses. (A) Gating strategy for identification of monocytes and macrophages. The peripheral blood is shown. Designation of population shown within each dot-plot is indicated above the dot-plot. Leukocytes were identified as viable (a) non-doublet (b) cells with typical light scatter properties of leukocytes (c). Then, macrophages were gated simply as CD203ahi leukocytes (d) and marked with blue color. Monocytes were gated as CD203alow/-SWC8-(e) CD172ahi(f) leukocytes where the CD203alow/- region was defined as the complementary region to the CD203ahi region. Then, SLA-DR+ monocytes were marked with red color and SLA-DR- monocytes were marked with green color (g). SLA-DR- region was defined as the complementary region to the SLA-DR+ region. Gating order is shown in the scheme (h). (B) Representative CD163 vs. CD14 dot-plots of macrophages (blue) and monocyte subpopulations (green: SLA-DR–, red: SLA-DR+) in various body compartments of control and APP-infected pigs. From: Ondrackova P, Leva L, Kucerova Z, Vicenova M, Mensikova M, Faldyna M. Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines. Vet Res. 2013 Oct 17;44:98. | |
Published customer image: Mouse anti Pig CD14, clone MIL2 used for the separation of mococytes from porcine PBMCs by immunomagnetic cell sorting. Image caption: Porcine MoDCs at different culture times (400×).CD14+ monocytes were purified from porcine PBMCs and were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS), 25 ng/mL recombinant porcine IL-4, and 10 ng/ml recombinant porcine GM-CSF. The culture medium was replenished every 3 days. (A) CD14+ monocytes after 2 days of culture. (B) CD14+ monocytes 3 days of culture. (C) CD14+ monocytes after 4 days of culture. (D) CD14+ monocytes after 5 days of culture. From: Citation: Liu J, Tian Z-Y, Xiao Y-C, Wang X-L, Jin M-L, Shi D-S (2016) The Role of Porcine Monocyte Derived Dendritic Cells (MoDC) in the Inflammation Storm Caused by Streptococcus suis Serotype 2 Infection. PLoS ONE 11(3): e0151256. | |
Figure A. FITC conjugated mouse anti porcine CD14 (MCA1218F) and A647 conjugated mouse IgG1 isotype control (MCA928A647). Figure B. FITC conjugated mouse anti porcine CD14 (MCA1218F) and A647 conjugated mouse anti porcine CD45 (MCA1222A647). All experiments performed on red cell lysed porcine blood gated on mononuclear cells. | |
Figure A. A647 conjugated mouse anti porcine CD45 (MCA1222A647) and FITC conjugated mouse IgG2b isotype control (MCA691F). Figure B. A647 conjugated mouse anti porcine CD45 (MCA1222A647) and FITC conjugated mouse anti porcine CD14 (MCA1218F). All experiments performed on red cell lysed porcine blood gated on mononuclear cells. |
