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인용 및 참조 문헌 (14)
Invitrogen™
FluoReporter™ Blue Fluorometric dsDNA Quantitation Kit, 200-2,000 assays
The FluoReporter™ Blue Fluorometric dsDNA Quantitation Kit provides the protocols and reagents for analyzing cellular NA with the blue-fluorescent Hoechst자세히 알아보기
| 카탈로그 번호 | 수량 |
|---|---|
| F2962 | 1 kit |
카탈로그 번호 F2962
제품 가격(KRW)
397,000
Exklusiv online
Ends: 31-Mar-2026
466,000할인액 69,000 (15%)
Each
수량:
1 kit
제품 가격(KRW)
397,000
Exklusiv online
Ends: 31-Mar-2026
466,000할인액 69,000 (15%)
Each
The FluoReporter™ Blue Fluorometric dsDNA Quantitation Kit provides the protocols and reagents for analyzing cellular NA with the blue-fluorescent Hoechst 33258 nucleic acid stain. With this kit, quantitation of cellular DNA is rapid, and all manipulations can be carried out in microplate wells. The cells are lysed by freezing them in distilled water, the diluted dye solution is then added to the lysed cells, and fluorescence is measured.
For Research Use Only. Not for use in diagnostic procedures.
사양
용도(장비)Microplate Reader
제품라인FluoReporter
제품 유형dsDNA Quantitation Kit
수량1 kit
배송 조건Room Temperature
검출 방법Fluorescence
형식96-well Plate
라벨 또는 염료Other Labels or Dyes
Unit SizeEach
구성 및 보관
Store in refrigerator (2–8°C) and protect from light.
자주 묻는 질문(FAQ)
Can I use Hoechst dyes to do both DNA quantitation and cell number counting in plates?
인용 및 참조 문헌 (14)
인용 및 참조 문헌
Abstract
Dominant-negative C/EBP disrupts mitotic clonal expansion and differentiation of 3T3-L1 preadipocytes.
Journal:Proc Natl Acad Sci U S A
PubMed ID:14688407
'Hormonal induction of growth-arrested 3T3-L1 preadipocytes rapidly activates expression of CCAAT/enhancer-binding protein (C/EBP) beta. Acquisition of DNA-binding activity by C/EBPbeta, however, is delayed until the cells synchronously enter the S phase of mitotic clonal expansion (MCE). After MCE, C/EBPbeta activates expression of C/EBPalpha and peroxisome proliferator-activated receptor gamma, which then
In vivo imaging platform for tracking immunotherapeutic cells.
Journal:Nat Biotechnol
PubMed ID:16041364
Cellular therapeutics show great promise for the treatment of disease, but few noninvasive techniques exist for monitoring the cells after administration. Here we present a magnetic resonance imaging (MRI) technology that uses perfluoropolyether (PFPE) agents to track cells in vivo. Fluorine MRI selectively images only the labeled cells, and a
ATP regulates the differentiation of mammalian skeletal muscle by activation of a P2X5 receptor on satellite cells.
Journal:J Cell Biol
PubMed ID:12135987
ATP is well known for its role as an intracellular energy source. However, there is increasing awareness of its role as an extracellular messenger molecule (Burnstock, 1997). Although evidence for the presence of receptors for extracellular ATP on skeletal myoblasts was first published in 1983 (Kolb and Wakelam), their physiological
5-HT2A receptor induces ERK phosphorylation and proliferation through ADAM-17 tumor necrosis factor-alpha-converting enzyme (TACE) activation and heparin-bound epidermal growth factor-like growth factor (HB-EGF) shedding in mesangial cells.
Journal:J Biol Chem
PubMed ID:16737974
In this study, we present multiple lines of evidence to support a critical role for heparin-bound EGF (epidermal growth factor)-like growth factor (HB-EGF) and tumor necrosis factor-alpha-converting enzyme (TACE) (ADAM17) in the transactivation of EGF receptor (EGFR), ERK phosphorylation, and cellular proliferation induced by the 5-HT(2A) receptor in renal mesangial
Small proline-rich repeat 3 is a novel coordinator of PDGFRβ and integrin β1 crosstalk to augment proliferation and matrix synthesis by cardiac fibroblasts.
Journal:FASEB J
PubMed ID:32297675