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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
20 Results for "
background fluorescence
" in MedChemExpress (MCE) Product Catalog:
Products (20)
20 Results for "background fluorescence" in MCE Product Catalog:
21
21 Publications Verification
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1 Cited Publications
Cat. No.: HY-D1540
CAS No.: 2097714-45-7
Synonyms: Cy 5.5 amine; Lumiprobe Cy 5.5 amine
Cat. No.: HY-D0102
CAS No.: 91366-65-3
Synonyms: ABD-F
Cat. No.: HY-DY1047
CAS No.: 1539318-36-9
Solvent and concentration: DMSO: 20 mM
Cat. No.: HY-D1346
CAS No.: 1877282-17-1
Cat. No.: HY-143285
Cat. No.: HY-164867
CAS No.: 3023933-33-4
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Fmoc-L-Dap(NBSD)-OH is a benzodiazole amino acid that can be used as a building block for constructing background-free peptide probes for fluorescence imaging .
Cat. No.: HY-D1426
CAS No.: 217176-86-8
Cat. No.: HY-D3206
CAS No.: 1860808-05-4
Cat. No.: HY-D2924
Cat. No.: HY-110251R
CAS No.: 1539318-36-9
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DFHBI-1T (Standard) is the analytical standard of DFHBI-1T (HY-110251). This product is intended for research and analytical applications. DFHBI-1T is a membrane-permeable RNA aptamers-activated fluorescence probe (ex/em=472 nm/507 nm). DFHBI-1T binds to RNA aptamers (Spinach, Spinach2, iSpinach, and Broccoli) and causes specific fluorescence and lower background fluorescence. DFHBI-1T is used to image RNA in live cells .
Cat. No.: HY-D3603
CAS No.: 928817-42-9
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Research Areas:
Benzylguanine-CY5 is a quenched fluorescent dye conjugate based on benzylguanine (BG). Benzylguanine-CY5 possesses the activity of specifically covalently labeling SNAP-tag fusion proteins. Benzylguanine-CY5 exhibits intramolecular fluorescence quenching in the unbound state; upon binding to SNAP-tag, the quenching guanine moiety is cleaved, and its fluorescence intensity increases. Benzylguanine-CY5 can be used for background-free specific fluorescent labeling and imaging studies of SNAP-tag fusion proteins in living cells .
Cat. No.: HY-D3361
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Research Areas:
JF639-HTL is a deep-red fluorescent dye belonging to the Janelia Fluor series and also a HaloTag ligand. JF639-HTL contains a methoxy group as the R substituent, which forms a specific covalent bond with HaloTag fusion proteins. JF639-HTL is fluorogenic, exhibiting low background fluorescence in solution and a significant fluorescence enhancement upon binding to proteins. It also possesses cell permeability and excellent photostability. JF639-HTL can be used in studies related to fluorescent labeling, localization tracking, and pulse-chase imaging of proteins in living cells .
Cat. No.: HY-D1346A
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Research Areas:
610CP TFA is a new type of actin labeling dye. It dissolves in organic solvents. In DMSO the 610CP TFA excitation/emission wavelength is between 609 and 634 nm. 610CP TFA is a fluorescent dye that penetrates living cells. Upon cell entry, 610CP TFA binds to Bromo-des-methyl-Jasplakinolide Therefore, 610CP TFA dye can be used to stain actin fluorescence images with low background and high resolution.
Cat. No.: HY-D3174
CAS No.: 2688758-23-6
Cat. No.: HY-D3007
Cat. No.: HY-D3391
Cat. No.: HY-DY2041
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Research Areas:
Callose Staining Solution (Aniline Blue, Bright-Field Method) is a fluorescent dye used for detecting callose in plant tissues, green algal cell walls, plant cells, and protoplasts. Callose Staining Solution (Aniline Blue, Bright-Field Method) specifically binds to callose, a β-(1,3)-D-glucan polymer, and exhibits blue-green fluorescence under alkaline conditions with reduced background staining and non-toxicity to living cells. Callose Staining Solution (Aniline Blue, Bright-Field Method) is suitable for observation under UV or epifluorescence microscopy (Ex/Em = 365-370/397-509 nm). Callose Staining Solution (Aniline Blue, Bright-Field Method) can be used in studies related to the visualization of callose deposition in plants .
Cat. No.: HY-D3525
Target:
Research Areas:
BDL-E5 is a fluorescent probe for detecting live induced pluripotent stem cells at the early reprogramming stage. Its detection mechanism involves specific binding to authentic reprogramming cells, which exhibit increased expression of pluripotency and epithelial genes and decreased expression of mesenchymal genes compared to non-reprogramming cells; it appears to co-localize more significantly with the Golgi complex than other organelle markers in reprogramming cells, and it does not require washing after staining to reduce background signals; fluorescence is generated upon binding to these early reprogramming cells, with positive cells appearing 7 days before iPS colonies are visible and stain positive for the conventional pluripotent marker TRA-1-60, and sorting BDL-E5-positive cells enriches populations that generate higher numbers and quality of iPS colonies. Its detection wavelength is Ex/Em = 578/599 nm .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
