cyanine7 5 amine cy7 5 Search Results


94
Lumiprobe cyanine7 5 amine dye cy7 5
Cyanine7 5 Amine Dye Cy7 5, supplied by Lumiprobe, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cyanine7 5 amine dye cy7 5 - by Bioz Stars, 2026-06
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94
Lumiprobe cy7 5 amine
Cy7 5 Amine, supplied by Lumiprobe, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cy7 5 amine/product/Lumiprobe
Average 94 stars, based on 1 article reviews
cy7 5 amine - by Bioz Stars, 2026-06
94/100 stars
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94
Lumiprobe cyanine7 5 nhs ester
Cyanine7 5 Nhs Ester, supplied by Lumiprobe, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
cyanine7 5 nhs ester - by Bioz Stars, 2026-06
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94
Lumiprobe sulfo cyanine7 5
(a) Insulin lispro (lispro) with <t>sulfo-cy7.5</t> dye covalently attached to the epsilon amine of LysB28. (b) Custom-designed OR-PAM. (c) Vis-NIR light absorption spectra of sulfo-cy7.5 dye-labeled lispro, oxygenated blood (HbO 2 ), and deoxygenated blood (Hb). The values of blood absorption spectra were adopted from a compilation of Scott Prahl using data from N. Kollias, Wellman Laboratories, Harvard Medical School, Boston and W. B. Gratzer, Med. Res. Council Labs, Holly Hill, London.
Sulfo Cyanine7 5, supplied by Lumiprobe, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/sulfo cyanine7 5/product/Lumiprobe
Average 94 stars, based on 1 article reviews
sulfo cyanine7 5 - by Bioz Stars, 2026-06
94/100 stars
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93
Lumiprobe cyanine7 5 dimethyl cy7 5
(a) Insulin lispro (lispro) with <t>sulfo-cy7.5</t> dye covalently attached to the epsilon amine of LysB28. (b) Custom-designed OR-PAM. (c) Vis-NIR light absorption spectra of sulfo-cy7.5 dye-labeled lispro, oxygenated blood (HbO 2 ), and deoxygenated blood (Hb). The values of blood absorption spectra were adopted from a compilation of Scott Prahl using data from N. Kollias, Wellman Laboratories, Harvard Medical School, Boston and W. B. Gratzer, Med. Res. Council Labs, Holly Hill, London.
Cyanine7 5 Dimethyl Cy7 5, supplied by Lumiprobe, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cyanine7 5 dimethyl cy7 5/product/Lumiprobe
Average 93 stars, based on 1 article reviews
cyanine7 5 dimethyl cy7 5 - by Bioz Stars, 2026-06
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Image Search Results


(a) Insulin lispro (lispro) with sulfo-cy7.5 dye covalently attached to the epsilon amine of LysB28. (b) Custom-designed OR-PAM. (c) Vis-NIR light absorption spectra of sulfo-cy7.5 dye-labeled lispro, oxygenated blood (HbO 2 ), and deoxygenated blood (Hb). The values of blood absorption spectra were adopted from a compilation of Scott Prahl using data from N. Kollias, Wellman Laboratories, Harvard Medical School, Boston and W. B. Gratzer, Med. Res. Council Labs, Holly Hill, London.

Journal: bioRxiv

Article Title: Photoacoustic imaging reveals mechanisms of rapid-acting insulin formulations dynamics at the injection site

doi: 10.1101/2022.03.10.483309

Figure Lengend Snippet: (a) Insulin lispro (lispro) with sulfo-cy7.5 dye covalently attached to the epsilon amine of LysB28. (b) Custom-designed OR-PAM. (c) Vis-NIR light absorption spectra of sulfo-cy7.5 dye-labeled lispro, oxygenated blood (HbO 2 ), and deoxygenated blood (Hb). The values of blood absorption spectra were adopted from a compilation of Scott Prahl using data from N. Kollias, Wellman Laboratories, Harvard Medical School, Boston and W. B. Gratzer, Med. Res. Council Labs, Holly Hill, London.

Article Snippet: The sulfo-cyanine7.5 (sulfo-cy7.5) labeled insulin analog was generated by selective acylation of the B-chain lysine B28 epsilon amino group of biosynthetic B28K, B29P-HI (insulin lispro), sourced from internal production, using a commercially available NHS ester from Lumiprobe.

Techniques: Labeling

Absorption of sulfo-cy7.5 dye-labeled lispro in either Humalog (a) and Lyumjev (b) formulations in mouse ear. (c) Side-view images of the sulfo-cy7.5 dye-labeled lispro in Humalog and Lyumjev formulations depicting tissue expansion. (d) Comparison of expansions caused by the Humalog and Lyumjev formulations, n = 3. Vertical scale bar = 100 μm; horizontal scale bar = 500 μm. Green is the sulfo-cy7.5 dye-labeled lispro and red is the blood (label-free). Data represent mean ± standard error of the mean.

Journal: bioRxiv

Article Title: Photoacoustic imaging reveals mechanisms of rapid-acting insulin formulations dynamics at the injection site

doi: 10.1101/2022.03.10.483309

Figure Lengend Snippet: Absorption of sulfo-cy7.5 dye-labeled lispro in either Humalog (a) and Lyumjev (b) formulations in mouse ear. (c) Side-view images of the sulfo-cy7.5 dye-labeled lispro in Humalog and Lyumjev formulations depicting tissue expansion. (d) Comparison of expansions caused by the Humalog and Lyumjev formulations, n = 3. Vertical scale bar = 100 μm; horizontal scale bar = 500 μm. Green is the sulfo-cy7.5 dye-labeled lispro and red is the blood (label-free). Data represent mean ± standard error of the mean.

Article Snippet: The sulfo-cyanine7.5 (sulfo-cy7.5) labeled insulin analog was generated by selective acylation of the B-chain lysine B28 epsilon amino group of biosynthetic B28K, B29P-HI (insulin lispro), sourced from internal production, using a commercially available NHS ester from Lumiprobe.

Techniques: Labeling, Comparison

(a) Linear dependence of the measured total amounts of the dye-labeled lispro on their injected amounts. Data (n = 3) represent mean ± standard deviation. (b) Comparison of injection-site absorption kinetics of the dye-labeled lispro (n = 4) and sulfo-cy7.5 dye (n = 3) in the Humalog and Lyumjev formulations. (c) Comparison of the fractional injection-site absorption for dye-labeled lispro in both formulations; n = 4. (d) Kinetic model fit on the mean of the absorption for dye-labeled lispro in both formulations; n = 4. (e) Comparison of t 1/2 (time required for 50% drug absorption). (f) Pharmacokinetic study in pigs for monomeric lispro (n = 15) in Humalog formulation without zinc and phenolic ligand, hexameric lispro (n = 16) in Humalog formulation, and hexameric lispro (n = 15) in Lyumjev formulation. Data represent mean ± standard error of the mean.

Journal: bioRxiv

Article Title: Photoacoustic imaging reveals mechanisms of rapid-acting insulin formulations dynamics at the injection site

doi: 10.1101/2022.03.10.483309

Figure Lengend Snippet: (a) Linear dependence of the measured total amounts of the dye-labeled lispro on their injected amounts. Data (n = 3) represent mean ± standard deviation. (b) Comparison of injection-site absorption kinetics of the dye-labeled lispro (n = 4) and sulfo-cy7.5 dye (n = 3) in the Humalog and Lyumjev formulations. (c) Comparison of the fractional injection-site absorption for dye-labeled lispro in both formulations; n = 4. (d) Kinetic model fit on the mean of the absorption for dye-labeled lispro in both formulations; n = 4. (e) Comparison of t 1/2 (time required for 50% drug absorption). (f) Pharmacokinetic study in pigs for monomeric lispro (n = 15) in Humalog formulation without zinc and phenolic ligand, hexameric lispro (n = 16) in Humalog formulation, and hexameric lispro (n = 15) in Lyumjev formulation. Data represent mean ± standard error of the mean.

Article Snippet: The sulfo-cyanine7.5 (sulfo-cy7.5) labeled insulin analog was generated by selective acylation of the B-chain lysine B28 epsilon amino group of biosynthetic B28K, B29P-HI (insulin lispro), sourced from internal production, using a commercially available NHS ester from Lumiprobe.

Techniques: Labeling, Injection, Standard Deviation, Comparison, Formulation