Note: You clicked on an external link, which has been disabled in order to keep your shopping session open.
|Tested species reactivity||Rabbit|
|Published species reactivity||Not Applicable|
|Host / Isotype||Goat / IgG|
|Immunogen||Gamma Immunoglobins Heavy and Light chains|
|Conjugate||Alexa Fluor® 660|
|Storage buffer||PBS, pH 7.5|
|Contains||5mM sodium azide|
|Storage Conditions||4° C, store in dark|
|Cross Adsorption||Against human IgG, human serum, mouse IgG, mouse serum and bovine serum|
|Antibody Form||Whole Antibody|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||1-10 µg/mL|
|Immunofluorescence (IF)||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 8 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||Structural and mechanistic insights into lunatic fringe from a kinetic analysis of enzyme mutants.||Luther KB,Schindelin H,Haltiwanger RS||The Journal of biological chemistry (284:3294)||2009|
|Not Applicable||Not Cited||The group B streptococcal alpha C protein binds alpha1beta1-integrin through a novel KTD motif that promotes internalization of GBS within human epithelial cells.||Bolduc GR,Madoff LC||Microbiology (Reading, England) (153:4039)||2007|
|Not Applicable||Not Cited||Breadth of tuning and taste coding in mammalian taste buds.||Tomchik SM,Berg S,Kim JW,Chaudhari N,Roper SD||The Journal of neuroscience : the official journal of the Society for Neuroscience (27:10840)||2007|
|Not Applicable||Not Cited||Emerin is hyperphosphorylated and redistributed in herpes simplex virus type 1-infected cells in a manner dependent on both UL34 and US3.||Leach N,Bjerke SL,Christensen DK,Bouchard JM,Mou F,Park R,Baines J,Haraguchi T,Roller RJ||Journal of virology (81:10792)||2007|
|Not Applicable||Not Cited||Cytolytic cells induce HMGB1 release from melanoma cell lines.||Ito N,DeMarco RA,Mailliard RB,Han J,Rabinowich H,Kalinski P,Stolz DB,Zeh HJ,Lotze MT||Journal of leukocyte biology (81:75)||2007|
|Not Applicable||Not Cited||Tyrosine phosphorylation of VE-cadherin prevents binding of p120- and beta-catenin and maintains the cellular mesenchymal state.||Potter MD,Barbero S,Cheresh DA||The Journal of biological chemistry (280:31906)||2005|
|Not Applicable||Not Cited||Evidence for a granule targeting sequence within platelet factor 4.||El Golli N,Issertial O,Rosa JP,Briquet-Laugier V||The Journal of biological chemistry (280:30329)||2005|
|Not Applicable||Not Cited||GABAergic synapses made by a retinal dopaminergic neuron.||Contini M,Raviola E||Proceedings of the National Academy of Sciences of the United States of America (100:1358)||2003|