|Flow Cytometry (Flow)||1-10 µg/mL|
|Immunocytochemistry (ICC)||4 µg/ml|
|Immunofluorescence (IF)||4 µg/ml|
|Miscellaneous PubMed (MISC)||See 2 publications below|
|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, store in dark|
|Cross Adsorption||Against human IgG and serum, mouse IgG and serum, and bovine serum|
|Antibody Form||Whole Antibody|
Allophycocyanin, Crosslinked, Goat Anti-Rabbit IgG (H+L) is prepared from crosslinked allophycocyanin (APC) and an affinity-purified goat anti-rabbit IgG antibody. Since this phycobiliprotein is optimally excited at 633 nm, it can also be excited at 594 nm; therefore, it can be used with samples simultaneously labeled with Texas Red dye or Alexa Fluor 594 dye without the need of a second excitation source. APC can be used in flow cytometry and imaging applications and is more photostable than Cy5 conjugates.
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.
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