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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® 594|
|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 11 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||GABAergic control of arteriolar diameter in the rat retina.||Hinds K,Monaghan KP,Frølund B,McGeown JG,Curtis TM||Investigative ophthalmology & visual science (54:6798)||2013|
|Not Applicable||Not Cited||Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis.||DeStefano GM,Fantauzzo KA,Petukhova L,Kurban M,Tadin-Strapps M,Levy B,Warburton D,Cirulli ET,Han Y,Sun X,Shen Y,Shirazi M,Jobanputra V,Cepeda-Valdes R,Cesar Salas-Alanis J,Christiano AM||Proceedings of the National Academy of Sciences of the United States of America (110:7790)||2013|
|Not Applicable||Not Cited||Dynamic interpretation of maternal inputs by the Drosophila segmentation gene network.||Liu F,Morrison AH,Gregor T||Proceedings of the National Academy of Sciences of the United States of America (110:6724)||2013|
|Not Applicable||Not Cited||GABAergic inhibition of histaminergic neurons regulates active waking but not the sleep-wake switch or propofol-induced loss of consciousness.||Zecharia AY,Yu X,Götz T,Ye Z,Carr DR,Wulff P,Bettler B,Vyssotski AL,Brickley SG,Franks NP,Wisden W||The Journal of neuroscience : the official journal of the Society for Neuroscience (32:13062)||2012|
|Not Applicable||Not Cited||Targeting green fluorescent protein to dendritic membrane in central neurons.||Kameda H,Furuta T,Matsuda W,Ohira K,Nakamura K,Hioki H,Kaneko T||Neuroscience research (61:79)||2008|
|Not Applicable||Not Cited||Identification of mouse Prp19p as a lipid droplet-associated protein and its possible involvement in the biogenesis of lipid droplets.||Cho SY,Shin ES,Park PJ,Shin DW,Chang HK,Kim D,Lee HH,Lee JH,Kim SH,Song MJ,Chang IS,Lee OS,Lee TR||The Journal of biological chemistry (282:2456)||2007|
|Not Applicable||Not Cited||Neuroanatomical evidence for segregation of nerve fibers conveying light touch and pain sensation in Eimer's organ of the mole.||Marasco PD,Tsuruda PR,Bautista DM,Julius D,Catania KC||Proceedings of the National Academy of Sciences of the United States of America (103:9339)||2006|
|Not Applicable||Not Cited||Selective permeability of different connexin channels to the second messenger cyclic AMP.||Bedner P,Niessen H,Odermatt B,Kretz M,Willecke K,Harz H||The Journal of biological chemistry (281:6673)||2006|
|Not Applicable||Not Cited||Phosphate deprivation induces transfer of DGDG galactolipid from chloroplast to mitochondria.||Jouhet J,Maréchal E,Baldan B,Bligny R,Joyard J,Block MA||The Journal of cell biology (167:863)||2004|
|Not Applicable||Not Cited||Photochemical gating of heterologous ion channels: remote control over genetically designated populations of neurons.||Zemelman BV,Nesnas N,Lee GA,Miesenbock G||Proceedings of the National Academy of Sciences of the United States of America (100:1352)||2003|
|Not Applicable||Not Cited||The metabotropic GABAB receptor directly interacts with the activating transcription factor 4.||Nehring RB,Horikawa HP,El Far O,Kneussel M,Brandstätter JH,Stamm S,Wischmeyer E,Betz H,Karschin A||The Journal of biological chemistry (275:35185)||2000|