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        1. 翌圣生物科技(上海)股份有限公司

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          670 phalloidin 鬼筆環(huán)肽 藍(lán)色熒光
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          初級(jí)會(huì)員·12年
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          曹女士
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          670 phalloidin 鬼筆環(huán)肽 藍(lán)色熒光 Fluorescent staining of fixed actin filaments in tissue sections and tissue culture cell preparations.Note: Unlike many actin antibodies, Acti-stain™ 670 phalloidin binds onl
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          670 phalloidin 鬼筆環(huán)肽 藍(lán)色熒光

          Product Uses Include
          ·                                 Fluorescent staining of fixed actin filaments in tissue sections and tissue culture cell preparations.Note: Unlike many actin antibodies, Acti-stain 670 phalloidin binds only to F-actin resulting in low background fluorescence. Furthermore, actin staining is not appreciably different between species.
          ·                                 Preparation of stabilized fluorescent actin filaments in vitro.
          Actin staining is very useful in determining the structure and function of the cytoskeleton in living and fixed cells. The actin cytoskeleton is a very dynamic and labile structure in the living cell, but it can be fixed with paraformaldehyde prior to probing or staining for actin structures.
          Material
          Phalloidin is a seven amino acid peptide toxin from the mushroom Amanita phalloides, which binds specifically and with high affinity (Kd 20 nM) to the polymerized form of actin (F-actin). Phalloidin lowers the critical concentration of actin polymerization to less than 1 µg/ml, thereby acting as a polymerization enhancer. Phalloidin has been labeled with a proprietary far-red fluorescent dye which allows it to be used to stain actin filaments in tissue cultured cells and tissue sections (1, see Figure 1)?and cell-free preparations. Acti-stain 670 phalloidin-labeled actin filaments retain many functional characteristics of unlabeled actin including their ability to interact with myosin. Actin-stain 670 phalloidin is supplied as a red solid.
          Note: Phalloidin is toxic and must be handled with care (LD50 human = 2mg/Kg).

          Example Results and Specifications

          Figure 1. Actin Stress Fibers stained with Acti-stain™ 670 in a Swiss 3T3 cell.

          Figure 2. Emission and excitation scans for Acti-stain™ phalloidins







          Mitotic Swiss 3T3 cell, F-actin stained with Acti-stain™ 670 (far-red, Cat. # PHDN1), nuclear DNA stained with Dapi (blue).

          Absorbance and fluorescence scan of Acti-stain™ 670. Labeled phalloidin was diluted into methanol and its absorbance and excitation spectra were scanned between 300-750 and 600-750 nm, respectively. Absorbance peaks at 625 nm and fluorescence at 675 nm.

          Acti-stain phalloidins are the most well characterized phalloidins available. Tabe 1 describes their brightness, photostability, background and affinity constants to F-actin. Compare these performance characteristics to other fluorescent phalloidins and you will see the advantages of using Acti-stain for your actin staining requirements.
          Table 1. Biochemical characteristics of fluorescent phalloidins


          Conjugate
          Cat.#
          Wavelengths (Ex/Em)
          Brightness (AFU*)
          Stability to photobleaching(half life in seconds**)
          Background (% of total AFU at 100nM**)
          Affinity (Kd in nanomolar)
          Fluorescein-phalloidin
          na
          485/535 FITC filter set
          432
          6
          22
          72 +/-12
          Acti-stain™ 488
          PHDG1
          485/535 FITC filter set
          832
          57
          5
          55 +/-8
          Acti-stain™ 535
          PHDR1
          535/585 TRITC filter set
          430
          27
          12
          36 +/-7
          Acti-stain™ 555
          PHDH1
          535/585 TRITC filter set
          551
          46
          16
          63 +/-8
          Acti-stain™ 670
          PHDN1
          640/680 Cy5 filter set
          332
          8
          18
          50 +/-12


          * = AFUs measured by quantitative cell imaging. ** = Measured in stained Swiss 3T3 cells in the absence of antifade.




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