Flow cytometry analysis of F(ab')2-Goat anti-Mouse IgG (H+L) Cross-Adsorbed Secondary Antibody, PE (Product # A10543) was performed using K-562 cells stained with alpha Tubulin Mouse Monoclonal Antibody (Product # A11126). 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 alpha Tubulin antibody (red histogram) at a dilution of 1:20 or a matched isotype control (pink histogram) in 2.5% BSA and incubated for 2 hours at room temperature. The cells were then labeled with F(ab')2-Goat anti-Mouse IgG (H+L) Cross-Adsorbed Secondary Antibody, PE (Product # A10543) 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. The green histogram represents no-primary-antibody control.
|Tested species reactivity||Mouse|
|Published species reactivity||Not Applicable|
|Host / Isotype||Goat / IgG|
|Immunogen||Gamma Immunoglobins Heavy and Light chains|
|Storage buffer||PBS, pH 7.5|
|Contains||5mM sodium azide|
|Storage Conditions||4° C|
|Cross Adsorption||Against human IgG and serum|
|Antibody Form||F(ab')2 Fragment|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||1:500|
* 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.
|Flow Cytometry (Flow)||See 2 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||
Quantitative Proteomic Verification of Membrane Proteins as Potential Therapeutic Targets Located in the 11q13 Amplicon in Cancers.
A10543 was used in flow cytometry to investigate alterations in surface protein expression associated with the 11q13 amplicon
|Hoover H,Li J,Marchese J,Rothwell C,Borawoski J,Jeffery DA,Gaither LA,Finkel N||Journal of proteome research (14:3670)||2015|
Dynamics of bivalent chromatin domains upon drug induced reactivation and resilencing in cancer cells.
A10543 was used in flow cytometry to investigate the epigenetic profiles of colonic cancer cells exposed to chromatin reactivating agents
|Mayor R,Muñoz M,Coolen MW,Custodio J,Esteller M,Clark SJ,Peinado MA||Epigenetics (6:1138)||2011|