FocalCheck™ Microspheres, 15 μm, fluorescent green ring stain/dark red throughout
FocalCheck™ Microspheres, 15 μm, fluorescent green ring stain/dark red throughout
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 striking자세히 알아보기
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카탈로그 번호수량
F7238
F-7238으로도 사용됨
0.5 mL
카탈로그 번호 F7238
F-7238으로도 사용됨
제품 가격(KRW)
592,000
온라인 행사
Ends: 31-Dec-2025
739,000
할인액 147,000 (20%)
Each
카트에 추가하기
수량:
0.5 mL
제품 가격(KRW)
592,000
온라인 행사
Ends: 31-Dec-2025
739,000
할인액 147,000 (20%)
Each
카트에 추가하기
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.

See our full collection of microscope calibration reagents ›

For Research Use Only. Not for use in diagnostic procedures.
사양
보정 유형Confocal Microscope Calibration
형식Suspension Beads
제품라인FocalCheck
수량0.5 mL
배송 조건Room Temperature
색상Dark Red, Green
직경(미터법)15 μm
제품 유형Microsphere
Unit SizeEach
구성 및 보관
Store in refrigerator 2°C to 8°C and protect from light.

인용 및 참조 문헌 (2)

인용 및 참조 문헌
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