IgG2A Isotype Controls
We offer IgG2A Isotype Controls for use in common research applications: Bioactivity, Blocking/Neutralizing, Control, ELISA, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry-Frozen, Immunohistochemistry-Paraffin, Immunoprecipitation, Western Blot. Each IgG2A Isotype Control is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our IgG2A Isotype Controls can be used in a variety of model species: Mouse, Rat. Use the list below to choose the IgG2A Isotype Control which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our IgG2A Isotype Controls.
Alternate Names for IgG2A Isotype Controls
12 Results for "igg2a" in Isotype Controls
![Immunoprecipitation: Mouse IgG2a Isotype Control (M2A) [NBP1-96778] - Cell lysates from T24 cells treated for 3h with vehicle or perifosine (0.5, 1 or 2.5 uM) were immunoprecipitated (IP) using a monoclonal anti-CB Ab. The immunoprecipitates were separated via 12% SDS-PAGE and then immunoblotted (IB) using Abs against phospho-tyrosine (pTyr) and CB. The lysates were also immunoprecipitated using isotype-matched IgG, which was used as a control. Image collected and cropped by CiteAb from the following publication (impactjournals.com/oncoscience/index.php?abs=147), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/Mouse-IgG2a-Isotype-Control-M2A-Immunoprecipitation-NBP1-96778-img0001.jpg "Immunoprecipitation: Mouse IgG2a Isotype Control (M2A) [NBP1-96778] - Cell lysates from T24 cells treated for 3h with vehicle or perifosine (0.5, 1 or 2.5 uM) were immunoprecipitated (IP) using a monoclonal anti-CB Ab. The immunoprecipitates were separated via 12% SDS-PAGE and then immunoblotted (IB) using Abs against phospho-tyrosine (pTyr) and CB. The lysates were also immunoprecipitated using isotype-matched IgG, which was used as a control. Image collected and cropped by CiteAb from the following publication (impactjournals.com/oncoscience/index.php?abs=147), licensed under a CC-BY license.")
![Immunoprecipitation: Mouse IgG2a Isotype Control (M2A) [NBP1-96778] - Cell lysates from T24 BC cells either untreated or treated with sorafenib (20 uM) for 1 or 3 h were immunoprecipitated (IP) using a monoclonal anti-CB Ab. The immunoprecipitates were separated via 12% SDS-PAGE and then immunoblotted (IB) using Abs against phospho-tyrosine (anti-pTyr) and CB. The lysates were also immunoprecipitated using isotype-matched IgG, which was used as a control. Image collected and cropped by CiteAb from the following publication (impactjournals.com/oncoscience/index.php?abs=147), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/Mouse-IgG2a-Isotype-Control-M2A-Immunoprecipitation-NBP1-96778-img0002.jpg)
![SDS-Page Results of Mouse IgG2a Isotype Control (M2A).Lane 1: Mouse IgG2a Isotype Control (M2A) Reduced [1.0ug]. Lane 2: Opal Prestained Molecular Weight Marker](http://images.novusbio.com/fullsize/nbp1-96778_mouse-monoclonal-mouse-igg2a-isotype-control-m2a-23520231821370.jpg)
![Flow Cytometry: Rat IgG2a Isotype Control (KLH/G2a-1-1) [NBP1-51104] - A cell surface stain was performed on RAW246.7 cells with B7-H1/PD-L1/CD274 (MIH5) antibody NBP1-43262APC (blue) and a matched isotype control NBP1-51104APC (orange). Cells were incubated in an antibody dilution of 0.5 ug/mL for 20 minutes at room temperature. Both antibodies were conjugated to Allophycocyanin.](http://images.novusbio.com/fullsize/Rat-IgG2a-Isotype-Control-KLH-G2a-1-1-Flow-Cytometry-NBP1-51104-img0001.jpg "Flow Cytometry: Rat IgG2a Isotype Control (KLH/G2a-1-1) [NBP1-51104] - A cell surface stain was performed on RAW246.7 cells with B7-H1/PD-L1/CD274 (MIH5) antibody NBP1-43262APC (blue) and a matched isotype control NBP1-51104APC (orange). Cells were incubated in an antibody dilution of 0.5 ug/mL for 20 minutes at room temperature. Both antibodies were conjugated to Allophycocyanin.")
![Immunofluorescence: Rat IgG2a Isotype Control (KLH/G2a-1-1) [NBP1-51104] - Frozen BALB/c mouse intestine tissue was stained with Rat IgG2a-UNLB isotype control (SB Cat. No. 0117-01; left) and Rat Anti-Mouse CD104-UNLB (SB Cat. No. 1855-01; right) followed by Goat Anti-Rat IgG(H+L), Mouse ads-BIOT (SB Cat. No. 3050-08), Streptavidin-FITC (SB Cat. No. 7100-02), and DAPI.](http://images.novusbio.com/fullsize/Rat-IgG2a-Isotype-Control-KLH-G2a-1-1-Immunofluorescence-NBP1-51104-img0002.jpg)
![Flow Cytometry: Rat IgG2a Isotype Control (2A3) [NBP2-21947] - Flow Cytometry: Rat IgG2a Isotype Control (2A3) [Alexa Fluor® 488] [NBP2-30137] - This image was submitted via customer review. Image using the Alexa Fluor 488 form of this antibody.](http://images.novusbio.com/fullsize/Rat-IgG2a-Isotype-Control-2A3-Flow-Cytometry-NBP2-21947-img0002.jpg "Flow Cytometry: Rat IgG2a Isotype Control (2A3) [NBP2-21947] - Flow Cytometry: Rat IgG2a Isotype Control (2A3) [Alexa Fluor® 488] [NBP2-30137] - This image was submitted via customer review. Image using the Alexa Fluor 488 form of this antibody.")
![Flow Cytometry: Rat IgG2a Isotype Control (2A3) [NBP2-21947] - Flow analysis of CD45R in 10^6 mouse splenocytes using 0.25 ug of this antibody. The shaded histogram represents mouse splenocytes alone; green represents rat isotype control (20211AF488); red represents this antibody.](http://images.novusbio.com/fullsize/Rat-IgG2a-Isotype-Control-2A3-Flow-Cytometry-NBP2-21947-img0001.jpg)
![Flow Cytometry: Mouse IgG2a Isotype Control (C1.18.4) [NBP2-14864] - Cell surface flow analysis of HLA-DR in human lymphocytes using at 1 ug/10^6 cells. Cells were stained with primary antibody followed by a PE-conjugated goat anti-mouse secondary antibody . Green represents isotype control (NBP2-14864); red represents anti-HLA-DR antibody.](http://images.novusbio.com/fullsize/Mouse-IgG2a-Isotype-Control-C1-18-4-Flow-Cytometry-NBP2-14864-img0002.jpg "Flow Cytometry: Mouse IgG2a Isotype Control (C1.18.4) [NBP2-14864] - Cell surface flow analysis of HLA-DR in human lymphocytes using at 1 ug/10^6 cells. Cells were stained with primary antibody followed by a PE-conjugated goat anti-mouse secondary antibody . Green represents isotype control (NBP2-14864); red represents anti-HLA-DR antibody.")