추천 제품
일반 설명
GlucoseCy5 is a cell-permeable, Cy5-linked 1-amino-1-deoxy-β-glucose fluorescent tracer. It is used for glucose transporter (GLUT)-mediated molecular sensing and bioimaging. GlucoseCy5 demonstrates superior specificity, sensitivity, and non-toxicity over 2-NBDG. λ emission & excitation ~ 644 nm & 665 nm. Suggested optimum concentration and incubation for cellular uptake: 50 μM & 20 min.
애플리케이션
GlucoseCy5 has been used as a component in serum-free Dulbecco′s modified eagle medium (DMEM) for fluorescence-activated cell sorting (FACS) and glucose-uptake assay.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Biochemical and biophysical research communications, 474(2), 240-246 (2016-04-02)
Two novel cyanine-based 1-amino-1-deoxy-β-glucose conjugates (Glu-1N-Cy3 and Glu-1N-Cy5) were designed, synthesized and their fluorescence characteristics were studied. Both Glu-1N-Cy3 and Glu-1N-Cy5 accumulate in living HT29 human colon cancer cells, which overexpress glucose transporters (GLUTs). The cellular uptake of the bioprobes
Transcriptional metabolic reprogramming implements meiotic fate decision in mouse testicular germ cells
Cell Reports (2023)
Metabolic support of tumour-infiltrating regulatory T cells by lactic acid
Nature (2021)
Nature, 591(7851), 645-651 (2021-02-17)
Regulatory T (Treg) cells, although vital for immune homeostasis, also represent a major barrier to anti-cancer immunity, as the tumour microenvironment (TME) promotes the recruitment, differentiation and activity of these cells1,2. Tumour cells show deregulated metabolism, leading to a metabolite-depleted
Biochemical and biophysical research communications, 480(3), 341-347 (2016-10-26)
Two novel fluorescent bioprobes, namely, 6N-Gly-Cy3 and 6N-Gly-Cy5, were designed and synthesized for real-time glucose transport imaging as well as potentially useful tracer for galactokinase metabolism. The structure of the bioprobes was fully characterized by 1H NMR, 13C NMR, IR
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