FocalCheck™ Microspheres, 15 μm, fluorescent green ring stain/dark red throughout
FocalCheck™ Microspheres, 15 μm, fluorescent green ring stain/dark red throughout
引用資料與參考文獻 (2)
Invitrogen™

FocalCheck™ Microspheres, 15 μm, fluorescent green ring stain/dark red throughout

The sharp ring stains exhibited by the 15 μm FocalCheck™ fluorescent green ring stained/dark red throughout microspheres produce a striking深入閱讀
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產品號碼Quantity
F7238
亦稱為 F-7238
0.5 mL
產品號碼 F7238
亦稱為 F-7238
價格 (HKD)
4,157.00
Each
新增至購物車
Quantity:
0.5 mL
價格 (HKD)
4,157.00
Each
新增至購物車
The sharp ring stains exhibited by the 15 μm FocalCheck™ fluorescent green ring stained/dark red throughout microspheres produce a striking visual representation of instrument misalignment or other aberrations making them ideal as reference standards for confocal laser-scanning microscopy. Correct image registration is indicated when the ring image and disk image of the combination beads are perfectly coincident in all dimensions.

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For Research Use Only. Not for use in diagnostic procedures.
規格
Calibration TypeConfocal Microscope Calibration
FormatSuspension Beads
Product LineFocalCheck
Quantity0.5 mL
Shipping ConditionRoom Temperature
ColorDark Red, Green
Diameter (Metric)15 μm
Product TypeMicrosphere
Unit SizeEach
內容物與存放
Store in refrigerator 2°C to 8°C and protect from light.

引用資料與參考文獻 (2)

引用資料與參考文獻
Abstract
Targeting of U2AF65 to sites of active splicing in the nucleus.
Authors:Gama-Carvalho M, Krauss RD, Chiang L, Valcárcel J, Green MR, Carmo-Fonseca M
Journal:J Cell Biol
PubMed ID:9166400
U2AF65 is an essential splicing factor that promotes binding of U2 small nuclear (sn)RNP at the pre-mRNA branchpoint. Here we describe a novel monoclonal antibody that reacts specifically with U2AF65. Using this antibody, we show that U2AF65 is diffusely distributed in the nucleoplasm with additional concentration in nuclear speckles, which ... More
Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts.
Authors:Sancataldo G, Gavryusev V, de Vito G, Turrini L, Locatelli M, Fornetto C, Tiso N, Vanzi F, Silvestri L, Pavone FS
Journal:Front Neuroanat
PubMed ID:30800060
The development of light-sheet fluorescence microscopy (LSFM) has greatly expanded the experimental capabilities in many biological and biomedical research fields, enabling for example live studies of murine and zebrafish neural activity or of cell growth and division. The key feature of the method is the selective illumination of a sample ... More