fluorometric-based lipase activity assay kit Search Results


fluorometric kit  (Cytoskeleton Inc)
96
Cytoskeleton Inc fluorometric kit
Fluorometric Kit, supplied by Cytoskeleton Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorometric-based+lipase+activity+assay+kit/pm31381339__jo9b01134_si_001-38-12-15?v=Cytoskeleton+Inc
Average 96 stars, based on 1 article reviews
fluorometric kit - by Bioz Stars, 2026-07
96/100 stars
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fluorometric-based l-lactate assay kit 6  (Cayman Chemical)
90
Cayman Chemical fluorometric-based l-lactate assay kit 6
Fluorometric Based L Lactate Assay Kit 6, supplied by Cayman Chemical, 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/fluorometric-based+lipase+activity+assay+kit/10__1161_slash_circresaha__116__310498-257-12-16?v=Cayman+Chemical
Average 90 stars, based on 1 article reviews
fluorometric-based l-lactate assay kit 6 - by Bioz Stars, 2026-07
90/100 stars
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hdac fluorometric activity assay kit  (Cayman Chemical)
90
Cayman Chemical hdac fluorometric activity assay kit
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Hdac Fluorometric Activity Assay Kit, supplied by Cayman Chemical, 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/fluorometric-based+lipase+activity+assay+kit/pmc05808772-514-6-14?v=Cayman+Chemical
Average 90 stars, based on 1 article reviews
hdac fluorometric activity assay kit - by Bioz Stars, 2026-07
90/100 stars
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amplite™ fluorimetric nadh assay kit  (AAT Bioquest)
90
AAT Bioquest amplite™ fluorimetric nadh assay kit
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Amplite™ Fluorimetric Nadh Assay Kit, supplied by AAT Bioquest, 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/fluorometric-based+lipase+activity+assay+kit/pmc06331054-556-15-20?v=AAT+Bioquest
Average 90 stars, based on 1 article reviews
amplite™ fluorimetric nadh assay kit - by Bioz Stars, 2026-07
90/100 stars
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amplitetm fluorimetric alkaline phosphatase assay kit (green fluorescence)  (AAT Bioquest)
90
AAT Bioquest amplitetm fluorimetric alkaline phosphatase assay kit (green fluorescence)
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Amplitetm Fluorimetric Alkaline Phosphatase Assay Kit (Green Fluorescence), supplied by AAT Bioquest, 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/fluorometric-based+lipase+activity+assay+kit/pmc06474890-85-8-16?v=AAT+Bioquest
Average 90 stars, based on 1 article reviews
amplitetm fluorimetric alkaline phosphatase assay kit (green fluorescence) - by Bioz Stars, 2026-07
90/100 stars
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fluorometric  (Thermo Fisher)
99
Thermo Fisher fluorometric
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Fluorometric, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorometric-based+lipase+activity+assay+kit/pmc06699926-82-5-14?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
fluorometric - by Bioz Stars, 2026-07
99/100 stars
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protein assay kit  (Thermo Fisher)
99
Thermo Fisher protein assay kit
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Protein Assay Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorometric-based+lipase+activity+assay+kit/10__3390_slash_pr8101228-89-15-18?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
protein assay kit - by Bioz Stars, 2026-07
99/100 stars
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fluorimetric cell-based glucose uptake assay kit #efgu-100  (BioAssay Systems LLC)
90
BioAssay Systems LLC fluorimetric cell-based glucose uptake assay kit #efgu-100
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Fluorimetric Cell Based Glucose Uptake Assay Kit #Efgu 100, supplied by BioAssay Systems LLC, 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/fluorometric-based+lipase+activity+assay+kit/pmc04930699-130-5-11?v=BioAssay+Systems+LLC
Average 90 stars, based on 1 article reviews
fluorimetric cell-based glucose uptake assay kit #efgu-100 - by Bioz Stars, 2026-07
90/100 stars
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ab138889  (Abcam)
99
Abcam ab138889
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Ab138889, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorometric-based+lipase+activity+assay+kit/pmc05992122-238-10-9?v=Abcam
Average 99 stars, based on 1 article reviews
ab138889 - by Bioz Stars, 2026-07
99/100 stars
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fluorescence based detection reagent  (Elabscience Biotechnology)
96
Elabscience Biotechnology fluorescence based detection reagent
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Fluorescence Based Detection Reagent, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorometric-based+lipase+activity+assay+kit/pmc11905655-58-13-16?v=Elabscience+Biotechnology
Average 96 stars, based on 1 article reviews
fluorescence based detection reagent - by Bioz Stars, 2026-07
96/100 stars
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dna concentration  (Thermo Fisher)
99
Thermo Fisher dna concentration
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Dna Concentration, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fluorometric-based+lipase+activity+assay+kit/bio_rxiv__2025__07__23__666010-58-16-23?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
dna concentration - by Bioz Stars, 2026-07
99/100 stars
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fluorometric-based lipase activity assay kit  (Cayman Chemical)
90
Cayman Chemical fluorometric-based lipase activity assay kit
Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, <t>HDAC</t> activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the <t>HDAC</t> <t>fluorometric</t> activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).
Fluorometric Based Lipase Activity Assay Kit, supplied by Cayman Chemical, 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/fluorometric-based+lipase+activity+assay+kit/10__3390_slash_ijms26125626-279-9-14?v=Cayman+Chemical
Average 90 stars, based on 1 article reviews
fluorometric-based lipase activity assay kit - by Bioz Stars, 2026-07
90/100 stars
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Image Search Results


Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, HDAC activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the HDAC fluorometric activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).

Journal: The Journal of Biological Chemistry

Article Title: Probing the interaction between the histone methyltransferase/deacetylase subunit RBBP4/7 and the transcription factor BCL11A in epigenetic complexes

doi: 10.1074/jbc.M117.811463

Figure Lengend Snippet: Pulldown assays show that BCL11A(2–16) peptide is sufficient to interact with PRC2, NuRD, and SIN3A epigenetic complexes in SUM149 cell lysate. A, amino acid sequences of the biotin-labeled BCL11A(2–16) WT and scramble (SCR) peptides used in our pulldown studies. B, Western blot analysis of RBBP4, RBBP7, HDAC1, HDAC2, and other components of PRC2 (EZH2 and SUZ12), NuRD (MTA1), SIN3A (SIN3A), and CoREST (CoREST) complexes following BCL11A(2–16) WT or scramble peptide pulldown. Ten micrograms of SUM149 whole-cell lysate (∼4.4% of the lysate used in the pulldown lanes) were loaded as a control for detection of the proteins of interest. C, HDAC activity assay following BCL11A(2–16) WT or scramble peptide pulldown was done using the HDAC fluorometric activity assay kit (Cayman Chemical). To determine the background fluorescence level, the pulldown samples were treated with 1 μm TSA, an HDAC inhibitor, before the assay. Results shown are mean ± S.D. (****, p < 0.0001, one-way analysis of variance). D, HDAC activity (nmol/min/ml) following BCL11A(2–16) WT or scramble peptide pulldown was calculated as described under “Materials and methods.” Results shown are mean ± S.D. (***, p < 0.001, Student's t test).

Article Snippet: HDAC activity was measured using the HDAC fluorometric activity assay kit (catalog no. 10011563, Cayman Chemical) following the manufacturer's instruction.

Techniques: Labeling, Western Blot, HDAC Activity Assay, Activity Assay, Fluorescence