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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® 633|
|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 4 publications below|
Flourescence of this long-wavelength Alexa Fluor dye is not visible by looking through a conventional fluorescence microscope.
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||The role of spartin and its novel ubiquitin binding region in DALIS occurrence.||Karlsson AB,Washington J,Dimitrova V,Hooper C,Shekhtman A,Bakowska JC||Molecular biology of the cell (25:1355)||2014|
|Not Applicable||Not Cited||Kappa opioid receptor activation of p38 MAPK is GRK3- and arrestin-dependent in neurons and astrocytes.||Bruchas MR,Macey TA,Lowe JD,Chavkin C||The Journal of biological chemistry (281:18081)||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||Precise localization of alpha7 nicotinic acetylcholine receptors on glutamatergic axon terminals in the rat ventral tegmental area.||Jones IW,Wonnacott S||The Journal of neuroscience : the official journal of the Society for Neuroscience (24:11244)||2004|