|Tested species reactivity||Chicken|
|Published species reactivity||Not Applicable|
|Host / Isotype||Goat / IgG|
|Immunogen||Gamma Immunoglobins Heavy and Light chains|
|Conjugate||Alexa Fluor® 546|
|Storage buffer||PBS, pH 7.5|
|Contains||5mM sodium azide|
|Storage Conditions||4° C, store in dark|
|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.
Anti-Chicken secondary antibodies are affinity-purified antibodies with well-characterized specificity for the chicken 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.
Loss of O-GlcNAc glycosylation in forebrain excitatory neurons induces neurodegeneration.
A-11040 was used in immunohistochemistry to characterize mice with a forebrain-specific loss of O-GlcNAc glycosylation
|Wang AC,Jensen EH,Rexach JE,Vinters HV,Hsieh-Wilson LC||Proceedings of the National Academy of Sciences of the United States of America (113:15120)||2016|
STAM2, a member of the endosome-associated complex ESCRT-0 is highly expressed in neurons.
A-11040 was used in immunocytochemistry and immunohistochemistry - frozen section to study STAM2 in the nervous system
|Kapuralin K,¿urlin M,Mitre¿i¿ D,Kosi N,Schwarzer C,Glavan G,Gajovi¿ S||Molecular and cellular neurosciences (67:104)||2015|
Boundary cap neural crest stem cells homotopically implanted to the injured dorsal root transitional zone give rise to different types of neurons and glia in adult rodents.
A-11040 was used in immunohistochemistry - frozen section to study the fate of mouse boundary cap neural crest stem cells implanted in the dorsal root transitional zone
|Trolle C,Konig N,Abrahamsson N,Vasylovska S,Kozlova EN||BMC neuroscience (15:null)||2014|
|Not Applicable||Not Cited||Axonal Localization of transgene mRNA in mature PNS and CNS neurons.||Willis DE,Xu M,Donnelly CJ,Tep C,Kendall M,Erenstheyn M,English AW,Schanen NC,Kirn-Safran CB,Yoon SO,Bassell GJ,Twiss JL||The Journal of neuroscience : the official journal of the Society for Neuroscience (31:14481)||2011|
|Not Applicable||Not Cited||Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa.||Yamashita T,Liu J,Gao J,LeNoue S,Wang C,Kaminoh J,Bowne SJ,Sullivan LS,Daiger SP,Zhang K,Fitzgerald ME,Kefalov VJ,Zuo J||The Journal of neuroscience : the official journal of the Society for Neuroscience (29:9748)||2009|
|Not Applicable||Not Cited||NAD+ activates KNa channels in dorsal root ganglion neurons.||Tamsett TJ,Picchione KE,Bhattacharjee A||The Journal of neuroscience : the official journal of the Society for Neuroscience (29:5127)||2009|
|Not Applicable||Not Cited||Acute regulation of aquaporin-2 phosphorylation at Ser-264 by vasopressin.||Fenton RA,Moeller HB,Hoffert JD,Yu MJ,Nielsen S,Knepper MA||Proceedings of the National Academy of Sciences of the United States of America (105:3134)||2008|
|Not Applicable||Not Cited||Pancreatic acinar cells express vesicle-associated membrane protein 2- and 8-specific populations of zymogen granules with distinct and overlapping roles in secretion.||Weng N,Thomas DD,Groblewski GE||The Journal of biological chemistry (282:9635)||2007|