CMTDP
CMTDP is a Fluorescent probe for detecting local polarity changes around the Cys34 domain of bovine serum albumin during pH-induced N→B conformational transition. It is a thiol-specific and polarity-sensitive probe; it covalently labels the free cysteine residue at position 34 (Cys34) of bovine serum albumin, and its fluorescence maximum emission wavelength shifts in response to solvent polarity, but not to pH and temperature. When labeled to BSA, as the local polarity around the Cys34 domain increases with rising pH, the probe shows a bathchromic shift in fluorescence emission wavelength and a decrease in fluorescence intensity, which allows quantification of the local polarity change via the relationship between emission wavelength shift and dielectric constant. CMTDP itself has absorption peaks at ~392 and 508 nm, and CMTDP-labeled BSA has excitation maxima at 376 and 470 nm at pH 6.0, with the shorter-wavelength excitation peak red-shifting as pH increases while the longer one remains stable; when excited at 470 nm, the fluorescence emission maximum shifts from 570 nm at pH 6.0 to 577 nm at pH 9.1, while free CMTDP at pH 7.4 has an emission maximum at 621 nm. The excitation/emission wavelengths for CMTDP-labeled BSA are Ex/Em = 376/570 nm at pH 6.0, Ex/Em = ~376+/573 nm at pH 7.4, Ex/Em = ~376+/575 nm at pH 8.0, Ex/Em = ~376+/577 nm at pH 9.1, and for free CMTDP at pH 7.4, Ex/Em (when excited at 470 nm) = 470/621 nm[1].
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- CAS 番号: 1027058-07-6
- 分子式: C28H21ClN8O3
- 分子量:552.97
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
Guide (The following is our recommended protocol. This protocol is for guidance only and should be modified according to your specific needs).
1. Stock Solution Preparation
1.1 Solvent: DMSO.
1.2 Concentration recommendation: 7.7 mM.
2. Working Solution Preparation
2.1 Diluent: 0.1 M Na₂HPO₄-NaH₂PO₄ buffer (pH 6.0, 7.4, 8.0) or 0.1 M Tris–HCl buffer (pH 9.1).
2.2 Working concentration: The final molar ratio of bovine serum albumin (BSA) to CMTDP is 1:1.
2.3 Note: Adjust working solution concentration as needed; prepare fresh before use.
3. Staining Procedure
3.1 Sample type: Protein sample (BSA).[1]
3.2 Incubation conditions: Incubate at 25°C for 3 h for pH 7.4, 8.0, 9.1; incubate at 25°C for 24 h for pH 6.0.
3.3 Washing steps: Dialyze reaction mixture against corresponding buffer solution through a 10 kDa molecular weight cutoff semi-permeable membrane; separate via Sephadex G-25 column with respective buffer as eluent; dialyze collected protein fraction against 0.03 M NH₄HCO₃ solution.
5. Detection & Analysis
5.1 Instrument: Fluorimeter.
5.1.1 Ex/Em wavelength: Excitation wavelength at 470 nm; maximum emission at 570 nm (pH 6.0), 573 nm (pH 7.4), 575 nm (pH 8.0), 577 nm (pH 9.1).
5.2 Result analysis:
5.2.1 Fluorescence intensity changes: Fluorescence intensity decreases with increasing pH.
5.2.2 Fluorescence localization: Localized at the Cys34 domain of BSA.
5.2.3 Color changes: Fluorescence emission shows a slight bathchromic (red) shift with increasing pH.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
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CAS 番号 1027058-07-6
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分子量 552.97
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分子式 C28H21ClN8O3
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SMILES
CC1=CC2=NC3=CC=C(C=C3N=C2C=C1NC4=NC(OC5=CC=C(C=C5)N6C(C=CC6=O)=O)=NC(Cl)=N4)N(C)C
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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.
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)