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qae sephadex a-25  (Millipore)


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    Structured Review

    Millipore qae sephadex a-25
    GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the <t>QAE-Sephadex</t> column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.
    Qae Sephadex A 25, supplied by Millipore, 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/qae-sephadex/sephadex+g+100/pmc12274924-5-0-4
    Average 90 stars, based on 1 article reviews
    qae sephadex a-25 - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Protocol to measure endogenous GlcNAc-1-phosphotransferase activity in SK-MEL-30 cells"

    Article Title: Protocol to measure endogenous GlcNAc-1-phosphotransferase activity in SK-MEL-30 cells

    Journal: STAR Protocols

    doi: 10.1016/j.xpro.2025.103935

    GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the QAE-Sephadex column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.
    Figure Legend Snippet: GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the QAE-Sephadex column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.

    Techniques Used: Enzyme Activity Assay, In Vitro, Enzymatic Assay, Activity Assay

    Setting up the in vitro GNPT assay (A) Drying down of the [ 3 H]UDP-GlcNAc donor molecule mixed with cold UDP-GlcNAc and ATP using a Speed Vac Concentrator attached to a cold trap that is connected to a vacuum pump. (B) Sonicator with attached microprobe used to prepare whole cell lysate. (C) Equilibration of QAE Sephadex column. (D) Binding of the reaction mixture to the QAE Sephadex column and washing of the column. (E and F) First and second elutions with 2 mM Tris buffer containing 30 mM NaCl. (G) Detecting counts in the elutions using a liquid scintillation counter.
    Figure Legend Snippet: Setting up the in vitro GNPT assay (A) Drying down of the [ 3 H]UDP-GlcNAc donor molecule mixed with cold UDP-GlcNAc and ATP using a Speed Vac Concentrator attached to a cold trap that is connected to a vacuum pump. (B) Sonicator with attached microprobe used to prepare whole cell lysate. (C) Equilibration of QAE Sephadex column. (D) Binding of the reaction mixture to the QAE Sephadex column and washing of the column. (E and F) First and second elutions with 2 mM Tris buffer containing 30 mM NaCl. (G) Detecting counts in the elutions using a liquid scintillation counter.

    Techniques Used: In Vitro, Binding Assay

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    Article Snippet: Degraded 3H-labeled cAMP was purified using QAE-Sephadex (Sigma) columns.

    Article Title: Core fucosylation of N-linked glycans in leukocyte adhesion deficiency/congenital disorder of glycosylation IIc fibroblasts.
    Article Snippet: Sephadex-G25, Sephadex-G10, QAE-Sephadex were from Sigma.

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    Article Title: Molecular cloning and characterization of the Caenorhabditis elegans alpha1,3-fucosyltransferase family.
    Article Snippet: The neutral reaction products were isolated by ion exchange chromatography on 0.5 mL columns of QAE-Sephadex (Sigma-Aldrich) to separate unincorporated label.

    Article Title: A picornaviral loop-to-loop replication complex
    Article Snippet: A total of 30 U of bovine thrombin (Roche) was added to the eluted fraction and this was dialyzed against 1 L of aqueous buffer containing 20 mM Tris, 1 mM DTT and 0.5 mM EDTA at pH 7.8 (buffer B) for 8 h with a change of buffer at 4 h. A QAE-Sephadex (Sigma–Aldrich) column was equilibrated with buffer B and the dialyzed protein fraction was passed through the column.

    Article Title: Spiders' digestive system as a source of trypsin inhibitors: functional activity of a member of atracotoxin structural family.
    Article Snippet: QAE-Sephadex (sigma: Q25120, 0.5 g) was resuspended in 12.5 ml of 25 mM ammonium bicarbonate (NH4HCO3) at pH 8.5 and incubated for 18 h at 25 °C, under agitation.

    Article Title: Analysis of Mannose 6-Phosphate Uncovering Enzyme Mutations Associated with Persistent Stuttering
    Article Snippet: UDP-GlcNAc, cycloheximide (CHX), α-methylmannoside, and QAE-Sephadex were from Sigma.

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    Ion Exchange Chromatography:

    Article Title: N termini of apPDE4 isoforms are responsible for targeting the isoforms to different cellular membranes.
    Article Snippet: Degraded 3H-labeled cAMP was purified using QAE-Sephadex (Sigma) columns.

    Article Title: Core fucosylation of N-linked glycans in leukocyte adhesion deficiency/congenital disorder of glycosylation IIc fibroblasts.
    Article Snippet: Sephadex-G25, Sephadex-G10, QAE-Sephadex were from Sigma.

    Article Title: An Aplysia Type 4 Phosphodiesterase Homolog Localizes at the Presynaptic Terminals of Aplysia Neuron and Regulates Synaptic Facilitation
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    Article Title: Molecular cloning and characterization of the Caenorhabditis elegans alpha1,3-fucosyltransferase family.
    Article Snippet: The neutral reaction products were isolated by ion exchange chromatography on 0.5 mL columns of QAE-Sephadex (Sigma-Aldrich) to separate unincorporated label.

    Article Title: A picornaviral loop-to-loop replication complex
    Article Snippet: A total of 30 U of bovine thrombin (Roche) was added to the eluted fraction and this was dialyzed against 1 L of aqueous buffer containing 20 mM Tris, 1 mM DTT and 0.5 mM EDTA at pH 7.8 (buffer B) for 8 h with a change of buffer at 4 h. A QAE-Sephadex (Sigma–Aldrich) column was equilibrated with buffer B and the dialyzed protein fraction was passed through the column.

    Article Title: Spiders' digestive system as a source of trypsin inhibitors: functional activity of a member of atracotoxin structural family.
    Article Snippet: QAE-Sephadex (sigma: Q25120, 0.5 g) was resuspended in 12.5 ml of 25 mM ammonium bicarbonate (NH4HCO3) at pH 8.5 and incubated for 18 h at 25 °C, under agitation.

    Article Title: Analysis of Mannose 6-Phosphate Uncovering Enzyme Mutations Associated with Persistent Stuttering
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    GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the <t>QAE-Sephadex</t> column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.
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    GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the <t>QAE-Sephadex</t> column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.
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    GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the <t>QAE-Sephadex</t> column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.
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    GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the <t>QAE-Sephadex</t> column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.
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    Image Search Results


    GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the QAE-Sephadex column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.

    Journal: STAR Protocols

    Article Title: Protocol to measure endogenous GlcNAc-1-phosphotransferase activity in SK-MEL-30 cells

    doi: 10.1016/j.xpro.2025.103935

    Figure Lengend Snippet: GlcNAc-1-phosphotransferase enzyme activity assay (A) Schematic diagram of the in vitro GNPT enzyme assay using with α-MM acceptor. The activity of endogenous GNPT in SK-MEL-30 whole cell lysates is measured to quantify the amount of α-MM-P-[ 3 H]GlcNAC reaction product that is formed in 1 hr. (B) The unreacted [ 3 H]UDP-GlcNAc donor molecule with two phosphates remains bound to the QAE-Sephadex column, while the α-MM-P-[ 3 H]GlcNAc reaction product with one phosphate elutes with 30 mM NaCl. ∗Note that there is invariably spontaneous breakdown of a very small amount of the [ 3 H]UDP-GlcNAc to [ 3 H]GlcNAc-1-P and UMP. The [ 3 H]GlcNAc-1-P will also bind to the column and elute with 30 mM NaCl to yield the background counts.

    Article Snippet: QAE Sephadex A-25 , MilliporeSigma , Cat#GE17-0190-01.

    Techniques: Enzyme Activity Assay, In Vitro, Enzymatic Assay, Activity Assay

    Setting up the in vitro GNPT assay (A) Drying down of the [ 3 H]UDP-GlcNAc donor molecule mixed with cold UDP-GlcNAc and ATP using a Speed Vac Concentrator attached to a cold trap that is connected to a vacuum pump. (B) Sonicator with attached microprobe used to prepare whole cell lysate. (C) Equilibration of QAE Sephadex column. (D) Binding of the reaction mixture to the QAE Sephadex column and washing of the column. (E and F) First and second elutions with 2 mM Tris buffer containing 30 mM NaCl. (G) Detecting counts in the elutions using a liquid scintillation counter.

    Journal: STAR Protocols

    Article Title: Protocol to measure endogenous GlcNAc-1-phosphotransferase activity in SK-MEL-30 cells

    doi: 10.1016/j.xpro.2025.103935

    Figure Lengend Snippet: Setting up the in vitro GNPT assay (A) Drying down of the [ 3 H]UDP-GlcNAc donor molecule mixed with cold UDP-GlcNAc and ATP using a Speed Vac Concentrator attached to a cold trap that is connected to a vacuum pump. (B) Sonicator with attached microprobe used to prepare whole cell lysate. (C) Equilibration of QAE Sephadex column. (D) Binding of the reaction mixture to the QAE Sephadex column and washing of the column. (E and F) First and second elutions with 2 mM Tris buffer containing 30 mM NaCl. (G) Detecting counts in the elutions using a liquid scintillation counter.

    Article Snippet: QAE Sephadex A-25 , MilliporeSigma , Cat#GE17-0190-01.

    Techniques: In Vitro, Binding Assay