Dye is moderate hydrophilic. ATTO 565, ATTO 590 and ATTO 594 are fluorescent labels belonging to the class of Rhodamine dyes. Terms Applicable to Registered Users of the Site. anti-SCNN1B Antikörper (Sodium Channel, Nonvoltage-Gated 1, beta) AA 617-638 (Atto 390) Primary Antibody SCNN1B Reaktivität: Human, Maus, Ratte, Hamster, Xenopus laevis ICC, IF, IP, IHC, WB Wirt: Kaninchen Polyclonal Atto 390 723. Atto 550 Archives - Leinco Technologies Effect of post-transfection time on flow cytometric resolution. Alexa Fluor® 555, ATTO 550, Cy®3, DyLight® 549, TRITC • Brighter than Cy®3 • Comparable to Alexa Fluor® 555 Yellow-Green 561 nm CF®568 562 583 Alexa Fluor® 568, ATTO 565, Rhodamine Red • Optimized for the 568 nm line of the Ar-Kr mixed-gas laser • Brighter and more photostable than Alexa Fluor® 568 CF®594 593 614 ATTO 550 is a fluorescent label related to Rhodamine 6G and Rhodamine B. Characteristic features of the label are strong absorption, high fluorescence quantum yield, and has high thermal and photo-stability. ATTO 550 consists of three isomers with practically identical absorption and fluorescence. Introduction to flow cytometry ATTO 542 has out standing flourescence intensity, it can be used to replace, Cy3 and Cy3B. Using flow cytometry, we analysed the IgM internalisation rate in cells activated with Abberior- or ATTO-FIP-IgM at different time points. Flow Cytometry Flow Cytometry (FACS), Immunofluorescence (IF) 产品特性 Rabbit anti-llama IgG (H&L) - Affinity Pure, DyLight 550 Conjugate. Fluorescence was analyzed on a BD FACSCalibur flow cytometer in the FL4 channel. Additionally the dye highly qualifies to be applied in flow cytometry (FACS), fluorescence in-situ hybridization (FISH) and many more. Crystals are read using 3 fluorescence channels and the Crystal Reader program. Anti-Mouse IgG2b (ATTO 550 Conjugated) Pre-adsorbed Secondary Antibody - Additional Information Shipping Condition Ambient Purity Anti-MOUSE IgG2b (Gamma 2b chain) Antibody was prepared from monospecific antiserum by immunoaffinity chromatography using antigens coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted …
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