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|Tested species reactivity||Guinea pig|
|Published species reactivity||Not Applicable|
|Host / Isotype||Goat / IgG|
|Immunogen||Gamma Immunoglobins Heavy and Light chains|
|Conjugate||Alexa Fluor® 568|
|Storage buffer||PBS, pH 7.5|
|Contains||5mM sodium azide|
|Storage Conditions||4° C, store in dark|
|Cross Adsorption||Against bovine, chicken, goat, hamster, human, mouse, rabbit, rat and sheep sera prior to conjugation|
|Antibody Form||Whole Antibody|
|Tested Applications||Dilution *|
|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 9 publications below|
Anti-Guinea Pig secondary antibodies are affinity-purified antibodies with well-characterized specificity for guinea pig 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||Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesion.||Winters T,McNicoll F,Jessberger R||The EMBO journal (33:1256)||2014|
|Not Applicable||Not Cited||Synaptic refinement of an inhibitory topographic map in the auditory brainstem requires functional Cav1.3 calcium channels.||Hirtz JJ,Braun N,Griesemer D,Hannes C,Janz K,Löhrke S,Müller B,Friauf E||The Journal of neuroscience : the official journal of the Society for Neuroscience (32:14602)||2012|
|Not Applicable||Not Cited||Alteration in neonatal nutrition causes perturbations in hypothalamic neural circuits controlling reproductive function.||Caron E,Ciofi P,Prevot V,Bouret SG||The Journal of neuroscience : the official journal of the Society for Neuroscience (32:11486)||2012|
|Not Applicable||Not Cited||Rotavirus NSP4 induces a novel vesicular compartment regulated by calcium and associated with viroplasms.||Berkova Z,Crawford SE,Trugnan G,Yoshimori T,Morris AP,Estes MK||Journal of virology (80:6061)||2006|
|Not Applicable||Not Cited||PAIR2 is essential for homologous chromosome synapsis in rice meiosis I.||Nonomura K,Nakano M,Eiguchi M,Suzuki T,Kurata N||Journal of cell science (119:217)||2006|
|Not Applicable||Not Cited||Stem cell division is regulated by the microRNA pathway.||Hatfield SD,Shcherbata HR,Fischer KA,Nakahara K,Carthew RW,Ruohola-Baker H||Nature (435:974)||2005|
|Not Applicable||Not Cited||Estrogens inhibit l-glutamate uptake activity of astrocytes via membrane estrogen receptor alpha.||Sato K,Matsuki N,Ohno Y,Nakazawa K||Journal of neurochemistry (86:1498)||2003|
|Not Applicable||Not Cited||Synaptotagmin V is targeted to dense-core vesicles that undergo calcium-dependent exocytosis in PC12 cells.||Saegusa C,Fukuda M,Mikoshiba K||The Journal of biological chemistry (277:24499)||2002|
|Not Applicable||Not Cited||Remodeling of the major pig xenoantigen by N-acetylglucosaminyltransferase III in transgenic pig.||Miyagawa S,Murakami H,Takahagi Y,Nakai R,Yamada M,Murase A,Koyota S,Koma M,Matsunami K,Fukuta D,Fujimura T,Shigehisa T,Okabe M,Nagashima H,Shirakura R,Taniguchi N||The Journal of biological chemistry (276:39310)||2001|