carboxyrhodamine 110 azide conjugates Search Results


6 carboxyrhodamine 110 peg3 azide  (Jena Bioscience)
93
Jena Bioscience 6 carboxyrhodamine 110 peg3 azide
6 Carboxyrhodamine 110 Peg3 Azide, supplied by Jena Bioscience, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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5 carboxyrhodamine 110 se  (Biotium)
90
Biotium 5 carboxyrhodamine 110 se
5 Carboxyrhodamine 110 Se, supplied by Biotium, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dbco peg4 rhodamine green fluorophore  (Jena Bioscience)
93
Jena Bioscience dbco peg4 rhodamine green fluorophore
Dbco Peg4 Rhodamine Green Fluorophore, supplied by Jena Bioscience, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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5/6-carboxyrhodamine 110-peg 3 -azide (bp-22478)  (BroadPharm)
90
BroadPharm 5/6-carboxyrhodamine 110-peg 3 -azide (bp-22478)
Clickable PiB derivative 3 was conjugated to an azide-labeled fluorophore to yield <t>5/6-carboxyrhodamine</t> 110-labeled PiB (4) (left arrow). Likewise, clickable PiB (3) was conjugated to 1 μm diameter azide-coated superparamagnetic beads to yield the magnetic bead PiB conjugate 5 (right arrow).
5/6 Carboxyrhodamine 110 Peg 3 Azide (Bp 22478), supplied by BroadPharm, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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acetylene peg4 biotin  (Jena Bioscience)
90
Jena Bioscience acetylene peg4 biotin
Clickable PiB derivative 3 was conjugated to an azide-labeled fluorophore to yield <t>5/6-carboxyrhodamine</t> 110-labeled PiB (4) (left arrow). Likewise, clickable PiB (3) was conjugated to 1 μm diameter azide-coated superparamagnetic beads to yield the magnetic bead PiB conjugate 5 (right arrow).
Acetylene Peg4 Biotin, supplied by Jena Bioscience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/carboxyrhodamine+110+azide+conjugates/5%2F6-Carboxyrhodamine+110-PEG4-Alkyne/pm33405877-53-57-58
Average 90 stars, based on 1 article reviews
acetylene peg4 biotin - by Bioz Stars, 2026-10
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dbco carboxyrhodamine 110  (Click Chemistry Tools)
86
Click Chemistry Tools dbco carboxyrhodamine 110
Clickable PiB derivative 3 was conjugated to an azide-labeled fluorophore to yield <t>5/6-carboxyrhodamine</t> 110-labeled PiB (4) (left arrow). Likewise, clickable PiB (3) was conjugated to 1 μm diameter azide-coated superparamagnetic beads to yield the magnetic bead PiB conjugate 5 (right arrow).
Dbco Carboxyrhodamine 110, supplied by Click Chemistry Tools, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/carboxyrhodamine+110+azide+conjugates/azide+biotin+peg3/pmc12528752-391-0-8
Average 86 stars, based on 1 article reviews
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5(6)-carboxyrhodamine 110  (AnaSpec)
90
AnaSpec 5(6)-carboxyrhodamine 110
The <t>R110</t> probe was synthesized via iterative Fmoc deprotection and amide coupling reactions (top). (A) LAP cleaves amino acid residues from the bisamide amino termini, restoring R110 fluorescence following LAP-mediated P1 cleavage. Amino acid side chain phosphorylation inhibits LAP exopeptidase activity. Low fluorescence intensity indicates PKA activity. (B) Assay LAP/PKA ratio was optimized on-chip using fixed [LAP] while varying [PKA]. Increasing [PKA] to the point that LAP activity became negligible had a modest effect on population mean, but greatly reduced the negative population’s spread; the assay Z′ (+/− PKA) increased from 0.57 to 0.72. (C) Under optimized conditions, H-9 was used as a positive control inhibitor of PKA (Z′ = 0.74). Normalized droplet fluorescence was taken as the ratio of signal in the 520- and 570-nm channels (probe:standard). Assays were incubated 17.6 min using the 2×-wide 2×-long ICEcreamer. Each histogram population represents 5,000 droplets.
5(6) Carboxyrhodamine 110, supplied by AnaSpec, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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carboxyrhodamine 110  (Biotium)
90
Biotium carboxyrhodamine 110
The <t>R110</t> probe was synthesized via iterative Fmoc deprotection and amide coupling reactions (top). (A) LAP cleaves amino acid residues from the bisamide amino termini, restoring R110 fluorescence following LAP-mediated P1 cleavage. Amino acid side chain phosphorylation inhibits LAP exopeptidase activity. Low fluorescence intensity indicates PKA activity. (B) Assay LAP/PKA ratio was optimized on-chip using fixed [LAP] while varying [PKA]. Increasing [PKA] to the point that LAP activity became negligible had a modest effect on population mean, but greatly reduced the negative population’s spread; the assay Z′ (+/− PKA) increased from 0.57 to 0.72. (C) Under optimized conditions, H-9 was used as a positive control inhibitor of PKA (Z′ = 0.74). Normalized droplet fluorescence was taken as the ratio of signal in the 520- and 570-nm channels (probe:standard). Assays were incubated 17.6 min using the 2×-wide 2×-long ICEcreamer. Each histogram population represents 5,000 droplets.
Carboxyrhodamine 110, supplied by Biotium, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/carboxyrhodamine+110+azide+conjugates/5-(AND-6)-CARBOXYRhodamine+%2C+SUCCIN/us09791450-1241-4-10
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biotium cas  (Biotium)
91
Biotium biotium cas
The <t>R110</t> probe was synthesized via iterative Fmoc deprotection and amide coupling reactions (top). (A) LAP cleaves amino acid residues from the bisamide amino termini, restoring R110 fluorescence following LAP-mediated P1 cleavage. Amino acid side chain phosphorylation inhibits LAP exopeptidase activity. Low fluorescence intensity indicates PKA activity. (B) Assay LAP/PKA ratio was optimized on-chip using fixed [LAP] while varying [PKA]. Increasing [PKA] to the point that LAP activity became negligible had a modest effect on population mean, but greatly reduced the negative population’s spread; the assay Z′ (+/− PKA) increased from 0.57 to 0.72. (C) Under optimized conditions, H-9 was used as a positive control inhibitor of PKA (Z′ = 0.74). Normalized droplet fluorescence was taken as the ratio of signal in the 520- and 570-nm channels (probe:standard). Assays were incubated 17.6 min using the 2×-wide 2×-long ICEcreamer. Each histogram population represents 5,000 droplets.
Biotium Cas, supplied by Biotium, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/carboxyrhodamine+110+azide+conjugates/6-CARBOXYRhodamine+110%2C+SE+(6-CR110%2C+SE)/pm37636047-226-111-110
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biotium cas - by Bioz Stars, 2026-10
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5-carboxyrhodamine 110 succinimidyl ester  (AnaSpec)
90
AnaSpec 5-carboxyrhodamine 110 succinimidyl ester
The <t>R110</t> probe was synthesized via iterative Fmoc deprotection and amide coupling reactions (top). (A) LAP cleaves amino acid residues from the bisamide amino termini, restoring R110 fluorescence following LAP-mediated P1 cleavage. Amino acid side chain phosphorylation inhibits LAP exopeptidase activity. Low fluorescence intensity indicates PKA activity. (B) Assay LAP/PKA ratio was optimized on-chip using fixed [LAP] while varying [PKA]. Increasing [PKA] to the point that LAP activity became negligible had a modest effect on population mean, but greatly reduced the negative population’s spread; the assay Z′ (+/− PKA) increased from 0.57 to 0.72. (C) Under optimized conditions, H-9 was used as a positive control inhibitor of PKA (Z′ = 0.74). Normalized droplet fluorescence was taken as the ratio of signal in the 520- and 570-nm channels (probe:standard). Assays were incubated 17.6 min using the 2×-wide 2×-long ICEcreamer. Each histogram population represents 5,000 droplets.
5 Carboxyrhodamine 110 Succinimidyl Ester, supplied by AnaSpec, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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azido peg3 carboxyrhodamine 110  (Thermo Fisher)
93
Thermo Fisher azido peg3 carboxyrhodamine 110
The <t>R110</t> probe was synthesized via iterative Fmoc deprotection and amide coupling reactions (top). (A) LAP cleaves amino acid residues from the bisamide amino termini, restoring R110 fluorescence following LAP-mediated P1 cleavage. Amino acid side chain phosphorylation inhibits LAP exopeptidase activity. Low fluorescence intensity indicates PKA activity. (B) Assay LAP/PKA ratio was optimized on-chip using fixed [LAP] while varying [PKA]. Increasing [PKA] to the point that LAP activity became negligible had a modest effect on population mean, but greatly reduced the negative population’s spread; the assay Z′ (+/− PKA) increased from 0.57 to 0.72. (C) Under optimized conditions, H-9 was used as a positive control inhibitor of PKA (Z′ = 0.74). Normalized droplet fluorescence was taken as the ratio of signal in the 520- and 570-nm channels (probe:standard). Assays were incubated 17.6 min using the 2×-wide 2×-long ICEcreamer. Each histogram population represents 5,000 droplets.
Azido Peg3 Carboxyrhodamine 110, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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carboxyrhodamine 110 hydrochloride  (Biotium)
90
Biotium carboxyrhodamine 110 hydrochloride
The <t>R110</t> probe was synthesized via iterative Fmoc deprotection and amide coupling reactions (top). (A) LAP cleaves amino acid residues from the bisamide amino termini, restoring R110 fluorescence following LAP-mediated P1 cleavage. Amino acid side chain phosphorylation inhibits LAP exopeptidase activity. Low fluorescence intensity indicates PKA activity. (B) Assay LAP/PKA ratio was optimized on-chip using fixed [LAP] while varying [PKA]. Increasing [PKA] to the point that LAP activity became negligible had a modest effect on population mean, but greatly reduced the negative population’s spread; the assay Z′ (+/− PKA) increased from 0.57 to 0.72. (C) Under optimized conditions, H-9 was used as a positive control inhibitor of PKA (Z′ = 0.74). Normalized droplet fluorescence was taken as the ratio of signal in the 520- and 570-nm channels (probe:standard). Assays were incubated 17.6 min using the 2×-wide 2×-long ICEcreamer. Each histogram population represents 5,000 droplets.
Carboxyrhodamine 110 Hydrochloride, supplied by Biotium, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/carboxyrhodamine+110+azide+conjugates/5-(AND-6)-CARBOXYRhodamine+110%2C+HYDROCHL/10__1002_slash_admi__201701163-243-4-11
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Image Search Results


Clickable PiB derivative 3 was conjugated to an azide-labeled fluorophore to yield 5/6-carboxyrhodamine 110-labeled PiB (4) (left arrow). Likewise, clickable PiB (3) was conjugated to 1 μm diameter azide-coated superparamagnetic beads to yield the magnetic bead PiB conjugate 5 (right arrow).

Journal: Bioconjugate chemistry

Article Title: Generation of clickable Pittsburgh Compound B for the detection and capture of β-amyloid in Alzheimer’s Disease brain

doi: 10.1021/acs.bioconjchem.7b00500

Figure Lengend Snippet: Clickable PiB derivative 3 was conjugated to an azide-labeled fluorophore to yield 5/6-carboxyrhodamine 110-labeled PiB (4) (left arrow). Likewise, clickable PiB (3) was conjugated to 1 μm diameter azide-coated superparamagnetic beads to yield the magnetic bead PiB conjugate 5 (right arrow).

Article Snippet: The reagents propargyl-PEG 3 -bromide (BP-22738) and 5/6-carboxyrhodamine 110-PEG 3 -azide (BP-22478) were obtained from BroadPharm Inc. (San Diego, California).

Techniques: Labeling

The R110 probe was synthesized via iterative Fmoc deprotection and amide coupling reactions (top). (A) LAP cleaves amino acid residues from the bisamide amino termini, restoring R110 fluorescence following LAP-mediated P1 cleavage. Amino acid side chain phosphorylation inhibits LAP exopeptidase activity. Low fluorescence intensity indicates PKA activity. (B) Assay LAP/PKA ratio was optimized on-chip using fixed [LAP] while varying [PKA]. Increasing [PKA] to the point that LAP activity became negligible had a modest effect on population mean, but greatly reduced the negative population’s spread; the assay Z′ (+/− PKA) increased from 0.57 to 0.72. (C) Under optimized conditions, H-9 was used as a positive control inhibitor of PKA (Z′ = 0.74). Normalized droplet fluorescence was taken as the ratio of signal in the 520- and 570-nm channels (probe:standard). Assays were incubated 17.6 min using the 2×-wide 2×-long ICEcreamer. Each histogram population represents 5,000 droplets.

Journal: Analytical chemistry

Article Title: Integrated, Continuous Emulsion Creamer

doi: 10.1021/acs.analchem.7b03070

Figure Lengend Snippet: The R110 probe was synthesized via iterative Fmoc deprotection and amide coupling reactions (top). (A) LAP cleaves amino acid residues from the bisamide amino termini, restoring R110 fluorescence following LAP-mediated P1 cleavage. Amino acid side chain phosphorylation inhibits LAP exopeptidase activity. Low fluorescence intensity indicates PKA activity. (B) Assay LAP/PKA ratio was optimized on-chip using fixed [LAP] while varying [PKA]. Increasing [PKA] to the point that LAP activity became negligible had a modest effect on population mean, but greatly reduced the negative population’s spread; the assay Z′ (+/− PKA) increased from 0.57 to 0.72. (C) Under optimized conditions, H-9 was used as a positive control inhibitor of PKA (Z′ = 0.74). Normalized droplet fluorescence was taken as the ratio of signal in the 520- and 570-nm channels (probe:standard). Assays were incubated 17.6 min using the 2×-wide 2×-long ICEcreamer. Each histogram population represents 5,000 droplets.

Article Snippet: Leucine aminopeptidase (LAP), Bovine serum albumin (BSA, Roche Diagnostics, Indianapolis, IN), polydimethylsiloxane (PDMS, Dow Corning, Midland, MI), 5(6)-carboxyrhodamine 110 (R110, Anaspec, Fremont, CA), c-AMP dependent protein kinase A (PKA, New England BioLabs, Ipswich, MA), phycoerythrin (Anaspec), 5(6)-carboxytetramethylrhodamine (TAMRA, Anaspec), and Taq DNA polymerase ( Taq , New England Biolabs) were used as provided.

Techniques: Synthesized, Fluorescence, Phospho-proteomics, Activity Assay, Positive Control, Incubation