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Check out the latest issue of BioProbes
FEATURED NEW PRODUCTS
what they are
how they work
|Product||Quantity||Species Reactivity||Applications||Cat. No.|
|Mnk1 [pT197/pT202] ABfinity™ Recombinant Rabbit Monoclonal Antibody||100 µg||Hu, B,* Ch,* Cn,* Cp,* Eq,* Mk,* Ms,* P,* Rt,* Sw,* X,* Z*||F, IF/ICC, WB||700242|
|T-bet ABfinity™ |
Recombinant Rabbit Monoclonal Antibody
|100 µg||Hu, Cp,* Mk*||F, IF/ICC, IHC, WB||700059|
|ERK1/2 [pT185/pY187] ABfinity™ Recombinant Rabbit Monoclonal Antibody||100 µg||Hu, B,* Ch,* Cp,* Ms,* Rt,* X,* Z*||E, IHC, WB||700012|
|JNK1-2 [pT183/pY185] ABfinity™ Recombinant Rabbit Monoclonal Antibody||100 µg||Hu, B,* Ch,* Cn,* Cp,* Eq,* Gf,* Mk,* Ms,* Ne*, P,* Or,* Rt,* Sw,* X,* Z*||E, IHC, WB||700031|
|JAK1 [pY1022/pY1023] ABfinity™ Recombinant Rabbit Monoclonal Antibody - Purified||100 µg||Hu, B,* Cn,* Cp,* Eq,* Mk,* Ms,* Rt,* Sw,* X,* Z*||WB||700028|
|ZAP-70 [pY315/pY319] ABfinity™ Recombinant Rabbit Monoclonal Antibody||100 µg||Ms, Ha,* Rt*||F, ICC, WB||700177|
|* Reactivity predicted but not tested. |
Reactivity: B = bovine; Ch = chicken; Cn = canine; Cp = chimpanzee; Eq = equine; Gf = goldfish; Ha = hamster; Hu = human; Mk = monkey (rhesus); Ms = mouse; Ne = nematode; P = primate; Or = orangutan; Rt = rat; Sw = swine; X = Xenopus; Z = zebrafish.
Applications: E = ELISA; F = flow cytometry; ICC = immunocytochemistry; IF = immunofluorescence; IHC = immunohistochemistry; WB = western blotting.
what it is
how it works
what it is
how it works
|Countess® Automated Cell Counter||1 each||C10227|
|Countess® Automated Cell Counter Starter Kit||1 kit||C10310|
|Countess® Automated Cell Counter Lab Starter Kit||1 kit||C10311|
|Countess® Cell Counting Chamber Slides, 1,250 slides (2,500 counts)||25 boxes||C10313|
|Countess® Cell Counting Chamber Slides, 2,500 slides (5,000 counts)||50 boxes||C10314|
|Countess® Cell Counting Chamber Slides, 5,000 slides (10,000 counts)||100 boxes||C10315|
|Maximize flow cytometry experiments |
Researchers today are trying to maximize the information they get out of flow cytometry experiments by looking at more parameters in a single sample. Qdot® nanocrystals provide a powerful way to multiply fluorophore selection using commonly available excitation sources. Invitrogen currently offers a growing selection of antibody conjugates using Qdot® 565, Qdot® 605, Qdot® 655, Qdot® 700, and Qdot® 800 nanocrystals.
Our research scientists have prepared an application note that describes tips and tricks, from sample preparation to filter selection, that will help you incorporate Qdot® nanocrystals into your phenotyping experiments.
This application note discusses:
|Advantages of using Qdot® nanocrystal primary antibody conjugates|
|Compatibility of Qdot® conjugates with common reagents used for sample preparation|
|Combining Qdot® conjugates with organic fluorescent conjugates|
|Filter optimization and instrument setup for use of Qdot® nanocrystal conjugates|
- Download the application note: Optimization of Qdot® nanocrystals for flow cytometry
- Learn More about Qdot® nanocrystal primary conjugates
Robust, Stackable 3D Cell Culture Environments
Derda R, Laromaine A, Mammoto A, Tang SKY, Mammoto T, Ingber DE, and Whitesides GM (2009) Paper-supported 3D cell culture for tissue-based bioassays. Proc Natl Acad Sci U S A 106(44):18457–18462.
Studies of cellular function using cultured cells are commonly performed in 2D environments that do not accurately replicate the oxygen and metabolite gradients that influence cells living in the 3D tissue environment. In an effort to more closely approximate the conditions of living tissue, Derda and colleagues created a cell suspension in gel matrix and spotted it onto chromatography paper. When they stacked several cell-infused papers vertically, a 3D culture environment was created, with layers at the top of the stack receiving more nutrient- and oxygen-rich culture medium and layers at the bottom receiving more depleted medium. Because the paper layers were sufficiently strong, stacking, culturing, and then destacking for analysis was simple. This allowed the researchers to look at the effects of oxygen and nutrient gradients without having to disrupt the 3D architecture of the cells in each layer.
As part of their investigation, the group studied each of the eight layers with respect to cell proliferation and DNA damage. They were able to confirm that cells in the lower layers contained significantly lower levels of S-phase entry (measured using the Click-iT® EdU Cell Proliferation Kit) and higher levels of DNA damage (measured using the Click-iT® TUNEL Alexa Fluor® 488 Imaging Assay) than cells in the top layer. By isolating RNA from the layers, the authors noted that cells furthest from the bulk medium not only showed the lowest proliferation but also had the highest expression of the hypoxia markers VEGF and IGFBP3, demonstrating that oxygen gradients (as opposed to nutrients or protons) are the major determinants of cell survival. The authors propose that the combination of paper and hydrogels provides a flexible, more realistic environment for cell biology research.
View the bibliography reference
- Learn More about Click-iT® EdU Cell Proliferation Assays
- Learn More about the Click-iT® TUNEL Assay for Apoptosis
|Click-iT® EdU Alexa Fluor® 488 Imaging Kit||1 kit||C10337|
|Click-iT® TUNEL Alexa Fluor® 488 Imaging Assay||1 kit||C10245|
|Phagocytosis in live macrophages.|
Phagocytosis in live mouse monocyte macrophages (mmm cells, ATCC TIB-67) was visualized by labeling with LysoTracker® Green DND-26 prior to incubating with pHrodo™ E. coli BioParticles® Phagocytosis Kit for Flow Cytometry. Cells were grown overnight, rinsed in prewarmed HBSS, then incubated for 5 min in LysoTracker® Green diluted 1:20,000 in HBSS. After washing 3 times with HBSS, pHrodo™ particles (50 µg/mL) were added and incubated for 10 min. As the pHrodo™ particles move into the lysosome, the low pH–responsive dye becomes brightly fluorescent. CellMask™ Deep Red Plasma Membrane Stain was then diluted to 5 µg/mL into HBSS for 5 min, and washed 3 times prior to imaging on a Nikon TE-200 Eclipse inverted microscope with a 40x objective using standard filter sets (FITC, TRITC, and Cy5). LysoTracker® dye is seen in green, pHrodo™ indicator in red, and CellMask™ Deep Red stain in purple.
|pHrodo™ E. coli BioParticles® Phagocytosis Kit for Flow Cytometry||1 kit||A10025|
|CellMask™ Deep Red Plasma Membrane Stain||100 µL||C10046|
|LysoTracker® Green DND-26||20 x 50 µL||L7526|
Thiol-Reactive Alexa Fluor® Dyes
In addition to offering expertly prepared dye conjugates, we also provide you with the opportunity to create your own fluorescent conjugates using reactive dyes. The Alexa Fluor® dyes—a series of superior fluorescent dyes that span the near-UV, visible, and near-IR spectrum—produce the best and brightest conjugates.
For selectively linking an Alexa Fluor® dye to accessible thiol groups on proteins or other molecules, Alexa Fluor® maleimides provide the easiest and most efficient reaction chemistry. Maleimides are excellent reagents for thiol modification, quantitation, and analysis, due to the stable thioether bond that is formed in the reaction.
With these reagents, you can vary both the amount of dye and the target in your labeling reaction to create the perfect Alexa Fluor® conjugate for your research application. The Alexa Fluor® maleimides are also useful for labeling the thiol-containing proteins on the surface of cells, where the polarity of the Alexa Fluor® dye permits sensitive detection of exposed thiols.
Cellular imaging with thiol-reactive Alexa Fluor® dyes. A431 cells incubated with green-fluorescent Alexa Fluor® 488 Transferrin, then fixed and permeabilized. Transferrin receptors were identified with anti–Transferrin Receptor, mouse IgG1 Monoclonal Antibody and visualized with red-fluorescent Alexa Fluor® 555 goat anti–mouse IgG antibody. Yellow fluorescence indicates regions of colocalization. Nuclei were stained with DAPI.
|Alexa Fluor® 350 C5 maleimide ||1 mg||A30505|
|Alexa Fluor® 488 C5 maleimide ||1 mg||A10254|
|Alexa Fluor® 532 C5 maleimide ||1 mg||A10255|
|Alexa Fluor® 546 C5 maleimide ||1 mg||A10258|
|Alexa Fluor® 555 C5 maleimide ||1 mg||A20346|
|Alexa Fluor® 568 C5 maleimide ||1 mg||A20341|
|Alexa Fluor® 594 C5 maleimide ||1 mg||A10256|
|Alexa Fluor® 633 C5 maleimide ||1 mg||A20342|
|Alexa Fluor® 647 C5 maleimide ||1 mg||A20347|
|Alexa Fluor® 680 C5 maleimide ||1 mg||A20344|
|Alexa Fluor® 750 C5 maleimide ||1 mg||A30459|
|Helping You Reduce Your Environmental Impact |
As a premier biotechnology company, we recognize that our first responsibility is to provide high-quality, high-performance products. Life Technologies is also committed to doing our part to minimize our footprint on the environment. Where possible, we believe it is our responsibility to provide you with sustainable product options. When you purchase selected Molecular Probes® products, you’ll notice less packaging but receive the same uncompromised performance.
|Alexa Fluor® Dye Selection Guide Widget|
The Alexa Fluor® Dye Selection Guide widget is designed to provide you with a concise and informative set of criteria for choosing the optimal Alexa Fluor® dye for your antibody or protein labeling application. Each page in this guide highlights a different Alexa Fluor® dye, summarizing key spectral data, excitation sources, and relevant product offerings. Full excitation and emission spectra are included for each of the dyes.
Molecular Probes® The Handbook
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