Muntjac cells were treated with 10 µM EdU (Cat. No. A10044) for 45 min; cells were then fixed and permeabilized, and EdU that had been incorporated into newly synthesized DNA was detected using the far red-fluorescent Click-iT™ EdU Alexa Fluor® 647 High-Throughput (HCS) Assay (Cat. No. A10208), utilizing the technical tip for converting the HCS assay to conventional fluorescence microscopy. Tubulin was labeled with an anti-alpha-tubulin antibody (Cat. No. A11126) and visualized with Alexa Fluor® 350 Goat Anti-Mouse IgG (Cat. No. A11045, A21049). The Golgi complex was stained with green-fluorescent Alexa Fluor® 488 conjugate of lectin HPA from Helix pomatia (edible snail) (Cat. No. L11271), and peroxisomes were labeled with an anti-peroxisome antibody and visualized with orange-fluorescent Alexa Fluor® 555 Donkey Anti-Rabbit IgG (Cat. No. A31572).
|Tested species reactivity||Rabbit|
|Published species reactivity||Not Applicable|
|Host / Isotype||Donkey / IgG|
|Immunogen||Gamma Immunoglobins Heavy and Light chains|
|Conjugate||Alexa Fluor® 555|
|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)||Assay Dependent|
|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.
These donkey anti-rabbit IgG (H+L)whole secondary antibodies have been affinity-purified and show minimum cross-reactivity. Cross-adsorption or pre-adsorption is a purification step to increase specificity of the antibody resulting in higher sensitivity and less background staining. The secondary antibody solution is passed through a column matrix containing immobilized serum proteins from potentially cross-reactive species. Only the nonspecific-binding secondary antibodies are captured in the column, and the highly specific secondaries flow through. The benefits of this extra step are apparent in multiplexing/multicolor-staining experiments (e.g., flow cytometry) where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there may be the presence of endogenous immunoglobulins.
Alexa Fluor dyes are among the most trusted fluorescent dyes available today. Invitrogen™ Alexa Fluor 555 dye is a bright, orange-fluorescent dye with excitation ideally suited to the 555 nm laser line. For stable signal generation in imaging and flow cytometry, Alexa Fluor 555 dye is pH-insensitive over a wide molar range. Probes with high fluorescence quantum yield and high photostability allow detection of low-abundance biological structures with great sensitivity. Alexa Fluor 555 dye molecules can be attached to proteins at high molar ratios without significant self-quenching, enabling brighter conjugates and more sensitive detection. The degree of labeling for each conjugate is typically 2-8 fluorophore molecules per IgG molecule; the exact degree of labeling is indicated on the certificate of analysis for each product lot.
Using conjugate solutions: Centrifuge the protein conjugate solution briefly in a microcentrifuge before use; add only the supernatant to the experiment. This step will help eliminate any protein aggregates that may have formed during storage, thereby reducing nonspecific background staining. Because staining protocols vary with application, the appropriate dilution of antibody should be determined empirically. For the fluorophore-labeled antibodies a final concentration of 1-10 µg/mL should be satisfactory for most immunohistochemistry and flow cytometry applications.
We offer an extensive line of Invitrogen™ secondary antibody conjugates with well-characterized specificity and labeled with a wide selection of premium fluorescent dyes, including Invitrogen™ Alexa Fluor™ fluorescent dyes. Fluorescent secondary antibody conjugates are useful in the detection, sorting, or purification of its specified target and ideal for fluorescence microscopy and confocal laser scanning microscopy, flow cytometry, and fluorescent western detection. The breadth of fluorescent markers we offer allows our reagents to be tailored to almost any fluorescent detection system.
Secondary antibodies may be provided in three formats: whole IgG, divalent F(ab')2 fragments, and monovalent Fab fragments. Because of the high degree of conservation in the structure of many immunoglobulin domains, most class-specific secondary antibodies must be affinity-purified and cross-adsorbed to achieve minimal cross-reaction with other immunoglobulins.
Our secondary antibody conjugates are most commonly prepared by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (e.g., immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents. In the first round of purification, whole immunoglobulins binding to the immunizing antibody are recovered and mainly consist of the ~150-kDa IgG class. Further purification, for example, with Protein A or G, removes all unwanted immunoglobulin classes except the affinity-purified antibodies that react with the target-specific immunoglobulin heavy and/or light chains.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Development of siRNA-loaded chitosan nanoparticles targeting Galectin-1 for the treatment of glioblastoma multiforme via intranasal administration.
A-31572 was used in immunohistochemistry to study targeting of Galectin-1 for the treatment of glioblastoma multiforme via intranasal administration by the development of siRNA-loaded chitosan nanoparticles
|Van Woensel M,Wauthoz N,Rosière R,Mathieu V,Kiss R,Lefranc F,Steelant B,Dilissen E,Van Gool SW,Mathivet T,Gerhardt H,Amighi K,De Vleeschouwer S||Journal of controlled release : official journal of the Controlled Release Society (227:71)||2016|
Using Ex Vivo Upright Droplet Cultures of Whole Fetal Organs to Study Developmental Processes during Mouse Organogenesis.
A-31572 was used in immunohistochemistry to study mouse organogenesis developmental processes using ex vivo upright droplet cultures of whole fetal fetal organs
|Potter SJ,DeFalco T||Journal of visualized experiments : JoVE (null:null)||2015|
|Not Applicable||Not Cited||
The methyl binding domain 3/nucleosome remodelling and deacetylase complex regulates neural cell fate determination and terminal differentiation in the cerebral cortex.
A-31572 was used in immunohistochemistry - frozen section to investigate the role of MBD3/NuRD in neurogenesis.
|Knock E,Pereira J,Lombard PD,Dimond A,Leaford D,Livesey FJ,Hendrich B||Neural development (10:null)||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-31572 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|
Foxg1 has an essential role in postnatal development of the dentate gyrus.
A-31572 was used in immunohistochemistry - frozen section to determine the function of Foxg1 in postnatal dentate gyrus neurogenesis.
|Tian C,Gong Y,Yang Y,Shen W,Wang K,Liu J,Xu B,Zhao J,Zhao C||The Journal of neuroscience : the official journal of the Society for Neuroscience (32:2931)||2012|
A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus.
A-31572 was used in immunocytochemistry to study pannexin-1 and it role in the activation of innate immune cells of the choroid plexus
|Maslieieva V,Thompson RJ||Channels (Austin, Tex.) (8:131)||2014|
|Not Applicable||Not Cited||Micron-scale spatially patterned, covalently immobilized vascular endothelial growth factor on hydrogels accelerates endothelial tubulogenesis and increases cellular angiogenic responses.||Leslie-Barbick JE,Shen C,Chen C,West JL||Tissue engineering. Part A (17:221)||2011|
|Not Applicable||Not Cited||Visualization and identification of IL-7 producing cells in reporter mice.||Mazzucchelli RI,Warming S,Lawrence SM,Ishii M,Abshari M,Washington AV,Feigenbaum L,Warner AC,Sims DJ,Li WQ,Hixon JA,Gray DH,Rich BE,Morrow M,Anver MR,Cherry J,Naf D,Sternberg LR,McVicar DW,Farr AG,Germain RN,Rogers K,Jenkins NA,Copeland NG,Durum SK||PloS one (4:null)||2009|
|Not Applicable||Not Cited||Generation of induced pluripotent stem cells using recombinant proteins.||Zhou H,Wu S,Joo JY,Zhu S,Han DW,Lin T,Trauger S,Bien G,Yao S,Zhu Y,Siuzdak G,Schöler HR,Duan L,Ding S||Cell stem cell (4:381)||2009|
|Not Applicable||Not Cited||Bryostatin-5 blocks stromal cell-derived factor-1 induced chemotaxis via desensitization and down-regulation of cell surface CXCR4 receptors.||He X,Fang L,Wang J,Yi Y,Zhang S,Xie X||Cancer research (68:8678)||2008|
|Not Applicable||Not Cited||Early resolution of acute immune activation and induction of PD-1 in SIV-infected sooty mangabeys distinguishes nonpathogenic from pathogenic infection in rhesus macaques.||Estes JD,Gordon SN,Zeng M,Chahroudi AM,Dunham RM,Staprans SI,Reilly CS,Silvestri G,Haase AT||Journal of immunology (Baltimore, Md. : 1950) (180:6798)||2008|
|Not Applicable||Not Cited||G-CSF rescues the memory impairment of animal models of Alzheimer's disease.||Tsai KJ,Tsai YC,Shen CK||The Journal of experimental medicine (204:1273)||2007|
|Not Applicable||Not Cited||Essential role of PDK1 in regulating endothelial cell migration.||Primo L,di Blasio L,Roca C,Droetto S,Piva R,Schaffhausen B,Bussolino F||The Journal of cell biology (176:1035)||2007|
|Not Applicable||Not Cited||Essential role of protein kinase C delta in platelet signaling, alpha IIb beta 3 activation, and thromboxane A2 release.||Yacoub D,Théorêt JF,Villeneuve L,Abou-Saleh H,Mourad W,Allen BG,Merhi Y||The Journal of biological chemistry (281:30024)||2006|
|Not Applicable||Not Cited||TGFbeta/activin/nodal signaling is necessary for the maintenance of pluripotency in human embryonic stem cells.||James D,Levine AJ,Besser D,Hemmati-Brivanlou A||Development (Cambridge, England) (132:1273)||2005|