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|Tested species reactivity||Mouse|
|Published species reactivity||Not Applicable|
|Host / Isotype||Goat / IgG|
|Immunogen||Mouse Mu immunonglobin|
|Storage buffer||PBS, pH 7.5|
|Contains||5mM sodium azide|
|Storage Conditions||4° C, store in dark|
|Cross Adsorption||Against human IgGl, IgG2a, IgG2b, IgG3, IgA, human serum and purified human paraproteins prior to conjugation|
|Antibody Form||Whole Antibody|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||1-10 µg/mL|
|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 8 publications below|
Flourescence of this long-wavelength Alexa Fluor dye is not visible by looking through a conventional fluorescence microscope.
Anti-Mouse secondary antibodies are affinity-purified antibodies with well-characterized specificity for mouse 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||Wandering neuronal migration in the postnatal vertebrate forebrain.||Scott BB,Gardner T,Ji N,Fee MS,Lois C||The Journal of neuroscience : the official journal of the Society for Neuroscience (32:1436)||2012|
|Not Applicable||Not Cited||Inflammatory cues modulate the expression of secretory product genes, Golgi sulfotransferases and sulfomucin production in LS174T cells.||Croix JA,Bhatia S,Gaskins HR||Experimental biology and medicine (Maywood, N.J.) (236:1402)||2011|
|Not Applicable||Not Cited||Profiling antibody responses by multiparametric analysis of primary B cells.||Story CM,Papa E,Hu CC,Ronan JL,Herlihy K,Ploegh HL,Love JC||Proceedings of the National Academy of Sciences of the United States of America (105:17902)||2008|
|Not Applicable||Not Cited||Editing and escape from editing in anti-DNA B cells.||Khan SN,Witsch EJ,Goodman NG,Panigrahi AK,Chen C,Jiang Y,Cline AM,Erikson J,Weigert M,Prak ET,Radic M||Proceedings of the National Academy of Sciences of the United States of America (105:3861)||2008|
|Not Applicable||Not Cited||Impact of image segmentation on high-content screening data quality for SK-BR-3 cells.||Hill AA,LaPan P,Li Y,Haney S||BMC bioinformatics (8:null)||2007|
|Not Applicable||Not Cited||Reactive oxygen species mediate central cardiorespiratory network responses to acute intermittent hypoxia.||Griffioen KJ,Kamendi HW,Gorini CJ,Bouairi E,Mendelowitz D||Journal of neurophysiology (97:2059)||2007|
|Not Applicable||Not Cited||Nucleosomes are exposed at the cell surface in apoptosis.||Radic M,Marion T,Monestier M||Journal of immunology (Baltimore, Md. : 1950) (172:6692)||2004|
|Not Applicable||Not Cited||Asymmetric localization of LGN but not AGS3, two homologs of Drosophila pins, in dividing human neural progenitor cells.||Fuja TJ,Schwartz PH,Darcy D,Bryant PJ||Journal of neuroscience research (75:782)||2004|