CyGbPF
CyGbPF is a granzyme B-specific near-infrared fluorescent probe. CyGbPF can be cleaved by granzyme B to remove the peptide cage group, restoring near-infrared fluorescence. CyGbPF passively accumulates in mouse tumors, and its activated fluorescence correlates with granzyme B expression, CD8+ cytotoxic T lymphocyte populations, and CD4+ helper T lymphocyte populations in tumor tissues. CyGbPF is efficiently cleared by the kidneys, enabling the assessment of immune activation via optical urine analysis. CyGbPF allows real-time non-invasive evaluation of cancer immunotherapeutic efficacy in living animals. CyGbPF can be used in research on cancers such as breast cancer. Excitation wavelength/emission wavelength: approximately 658 nm/approximately 717 nm.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 分子量:2000 (Average)
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
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生物活性
製品説明
体外実験
CyGbPF (2-250 μM; 5-90 min) is specifically cleaved by mouse granzyme B in cell-free assays, exhibiting a 24-fold near-infrared fluorescence enhancement[1].
CyGbPF (5 μM; 0.5-2.0 h; 1.60-200 μg/mL) is rapidly activated by endogenous granzyme B in CD8+ T cells, with a time-dependent fluorescence enhancement amplitude approximately 35-fold higher than that in 4T1 cells and approximately 15-fold higher than that in RAW264.7 cells; moreover, it exhibits only extremely low cytotoxicity at concentrations up to 200 μg/mL across all three cell lines[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
体内実験
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Balb/c (tumor-bearing, implanted with 4T1 breast cancer cells, pretreated with immunotherapeutic agents for immunoactivation)[1]
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Dosage:10 μM/kg
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Administration:i.v.; single dose
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Result:Reached maximum tumor NIRF signal intensity at 6 hours post-injection.
Showed tumor NIRF signals 1.47-fold (NLG919-pretreated), 1.54-fold (R848-pretreated), 2.23-fold (BMS-1-pretreated), 2.79-fold (pexidartinib-pretreated), and 2.85-fold (BEC-pretreated) higher than control mice at 6 hours post-injection.
Accumulated 14% of injected dose in tumors with negligible accumulation in other organs.
Correlated strongly with tumor tissue levels of granzyme B, CD8+ T cells, and CD4+ T cells, which were elevated in immunotherapy-treated mice relative to controls.
化学情報
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分子量 2000 (Average)
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SMILES
CC(N[C@@H]([C@H](CC)C)C(N[C@H](C(N[C@H](C(N[C@H](C(NC1=CC=C(C=C1)COC2=CC(OC3=C4/C=C/C(C(C)(C5=CC=CC=C56)C)=[N+]6CCCCN7C=C(COCCOC)N=N7)=C(C=C3CCC4)C=C2)=O)CC(O)=O)=O)CC8=CC=CC=C8)=O)CCC(O)=O)=O)=O.[I-].[n]
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
プロトコル
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RNA extraction experimental
By lysing cells, releasing RNA, and removing impurities such as proteins and DNA, high-purity RNA products are finally obtained. The commonly used traditional method is the guanidine isothiocyanate/phenol/chloroform method (Trizol), which is suitable for a variety of animal materials including animal tissues, microorganisms, cultured cells, etc., and most plant materials.
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Breast Cancer Modeling
Breast cancer is a heterogeneous cancer, and it has been distinguished into four subtypes: luminal A, luminal B, HER2-positive and basal-like. Molecular mutations, epigenetic alterations, hormone exposure and immune microenvironment are related to the progression of breast cancer.
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Cell Viability Determination by MTT Colorimetric Assay
The following protocol uses the MTT colorimetric assay as a classic literature-established method for assessing cell viability/metabolic activity in cultured mammalian cells. MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] is reduced by metabolically active cells to a colored formazan product; the amount of formazan is quantified spectrophotometrically and provides an indirect measure of metabolically active viable cells. Importantly, MTT reduction reflects cellular oxidoreductase/metabolic activity rather than an absolute direct count of living cells, so changes in cellular metabolism can alter the signal independently of cell number.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)