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Flow cytometry analysis of Goat anti-Rabbit IgG (H+L) Secondary Antibody, PE (P2771MP ) was performed using HeLa cells stained with HDAC4 ABfinity™ Rabbit Oligoclonal Antibody (711390). 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 HDAC4 ABfinity™ antibody or with rabbit 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-Rabbit IgG (H+L) Secondary Antibody, PE (P2771MP ) 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 HDAC4 ABfinity™ Oligoclonal Antibody respectively. Median fluorescence intensity from the three samples is compared in panel d.
|Tested species reactivity||Rabbit|
|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 mouse IgG, mouse serum and human serum|
|Antibody Form||Whole Antibody|
|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.
|Miscellaneous PubMed (MISC)||See 5 publications below|
Anti-Rabbit secondary antibodies are affinity-purified antibodies with well-characterized specificity for rabbit 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||Mast cell tryptase controls paracellular permeability of the intestine. Role of protease-activated receptor 2 and beta-arrestins.||Jacob C,Yang PC,Darmoul D,Amadesi S,Saito T,Cottrell GS,Coelho AM,Singh P,Grady EF,Perdue M,Bunnett NW||The Journal of biological chemistry (280:31936)||2005|
|Not Applicable||Not Cited||Quantitative analysis by flow cytometry of abscisic acid-inducible gene expression in transiently transformed rice protoplasts.||Hagenbeek D,Rock CD||Cytometry (45:170)||2001|
|Not Applicable||Not Cited||Mouse LYVE-1 is an endocytic receptor for hyaluronan in lymphatic endothelium.||Prevo R,Banerji S,Ferguson DJ,Clasper S,Jackson DG||The Journal of biological chemistry (276:19420)||2001|
|Not Applicable||Not Cited||Enhancement of ATP levels and glucose metabolism during an infection by Chlamydia. NMR studies of living cells.||Ojcius DM,Degani H,Mispelter J,Dautry-Varsat A||The Journal of biological chemistry (273:7052)||1998|
|Not Applicable||Not Cited||Rapid assessment of physiological status in Escherichia coli using fluorescent probes.||Porter J,Edwards C,Pickup RW||The Journal of applied bacteriology (79:399)||1995|