Flow cytometry analysis of Goat anti-Mouse IgG2b Secondary Antibody, Alexa Fluor 555 (A21147) was performed using Jurkat cells stained with E2F1 Mouse Monoclonal Antibody (321400). Cells were fixed with 70% ethanol for 10 minutes, permeabilized with 0.25% Triton™ X-100 for 20 minutes, and blocked with 5% BSA for 30 minutes at room temperature. Cells were labeled with E2F1 antibody or with mouse isotype control at 3-5 ug/million cells in 2.5% BSA and incubated for 2 hours at room temperature. The cells were then labeled with Goat anti-Mouse IgG2b Secondary Antibody, Alexa Fluor 555 (A21147) at a dilution of 1:500 for 1 hour at room temperature. A representative 10,000 cells were acquired and analyzed for each sample using the Attune® NxT Acoustic Focusing Cytometer. Panels a, b and c represent cells stained with the secondary antibody alone, isotype control and E2F1 Monoclonal Antibody respectively. Median fluorescence intensity from the three samples is compared in panel d.
|Tested species reactivity||Mouse|
|Published species reactivity||Not Applicable|
|Host / Isotype||Goat / IgG|
|Conjugate||Alexa Fluor® 555|
|Storage buffer||PBS, pH 7.5|
|Contains||5mM sodium azide|
|Storage Conditions||4° C, store in dark|
|Cross Adsorption||Against mouse IgM, mouse IgA, pooled human sera, purified human paraproteins and mouse isotypes IgG1, IgG2a and IgG3 prior to conjugation|
|Antibody Form||Whole Antibody|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||1:500|
|Immunocytochemistry (ICC)||1-10 µg/ml|
|Immunofluorescence (IF)||1-10 µg/mL|
|Immunohistochemistry (IHC)||1-10 µg/ml|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
|Miscellaneous PubMed (MISC)||See 4 publications below|
Anti-Mouse secondary antibodies are affinity-purified antibodies with well-characterized specificity for mouse immunoglobulins and are useful in the detection, sorting or purification of its specified target. Secondary antibodies offer increased versatility enabling users to use many detection systems (e.g. HRP, AP, fluorescence). They can also provide greater sensitivity through signal amplification as multiple secondary antibodies can bind to a single primary antibody. Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (i.e. immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
|Not Applicable||Not Cited||Discs large 1 (Dlg1) scaffolding protein participates with clathrin and adaptator protein complex 1 (AP-1) in forming Weibel-Palade bodies of endothelial cells.||Philippe M,Léger T,Desvaux R,Walch L||The Journal of biological chemistry (288:13046)||2013|
|Not Applicable||Not Cited||High-fat-diet exposure induces IgG accumulation in hypothalamic microglia.||Yi CX,Tschöp MH,Woods SC,Hofmann SM||Disease models and mechanisms (5:686)||2012|
|Not Applicable||Not Cited||GCC185 plays independent roles in Golgi structure maintenance and AP-1-mediated vesicle tethering.||Brown FC,Schindelhaim CH,Pfeffer SR||The Journal of cell biology (194:779)||2011|
|Not Applicable||Not Cited||Interaction of PRP4 with Kruppel-like factor 13 regulates CCL5 transcription.||Huang B,Ahn YT,McPherson L,Clayberger C,Krensky AM||Journal of immunology (Baltimore, Md. : 1950) (178:7081)||2007|