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詳細
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.
アプリケーション
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.
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
SML3233-VAR:
SML3233-BULK:
SML3233-5MG:
SML3233-25MG:
試験成績書(COA)
製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Metabolic support of tumour-infiltrating regulatory T cells by lactic acid
Nature (2021)
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
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
Transcriptional metabolic reprogramming implements meiotic fate decision in mouse testicular germ cells
Cell Reports (2023)
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
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