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  • 90
    ATCC rotavirus a rva human nca 125l 2010 g3p
    Rotavirus A Rva Human Nca 125l 2010 G3p, supplied by ATCC, 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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    97
    Thermo Fisher silencer gapdh sirna
    Silencer Gapdh Sirna, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 221 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore g3p
    Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate <t>(G3P)</t> and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.
    G3p, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 51 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Thermo Fisher human gapdh
    Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate <t>(G3P)</t> and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.
    Human Gapdh, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1080 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    96
    Thermo Fisher gapdh
    Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate <t>(G3P)</t> and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.
    Gapdh, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 14534 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Millipore g3p dehydrogenase
    Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate <t>(G3P)</t> and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.
    G3p Dehydrogenase, supplied by Millipore, used in various techniques. Bioz Stars score: 94/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    AstraZeneca g3p
    Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate <t>(G3P)</t> and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.
    G3p, supplied by AstraZeneca, 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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    92
    Mobitec anti phage g3p piii
    Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate <t>(G3P)</t> and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.
    Anti Phage G3p Piii, supplied by Mobitec, used in various techniques. Bioz Stars score: 92/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    95
    Thermo Fisher silencer cy3 labeled gapdh sirna
    Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate <t>(G3P)</t> and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.
    Silencer Cy3 Labeled Gapdh Sirna, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Abcam 1 acylglycerol 3 phosphate o acyltransferase abhd5
    Insulin sensitivity, hepatic omega fatty acid composition, and protein markers of stress kinases, lipid peroxidation, oxidative stress, lipid synthesis, and mitochondrial content in control-sedentary (C-Sed), ALA-sedentary (ALA-Sed), control-exercise (C-Ex), or ALA-exercise (ALA-Ex) group obese Zucker rats. AKT phosphorylation ( A ), hepatic n-3 and n-6 polyunsaturated fatty acids (PUFAs) ( B ), markers of mitochondrial content, stress kinases, antioxidants, oxidative stress, and TAG synthesis ( C ) in obese Zucker rats. C, control; EPA, eicosapentaenoic acid; DHA, docosahexaenoic acid; LA, linoleic acid; AA, arachidonic acid; CAT, catalase; SOD, superoxide dismutase; GPAT, <t>glycerol-3-phosphate</t> <t>acyltransferase;</t> DGAT, diacylglyceride transferase; 4HNE, 4-hydroxynonenal; JNK, c-jun NH 2 -terminal kinases; OD, optical density. Data are expressed as means ± SE; n = 5/group. “Main effect” represents Ex greater than Sed or ALA greater than C.
    1 Acylglycerol 3 Phosphate O Acyltransferase Abhd5, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 117 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    84
    AAT Bioquest amplite fluorimetric g3p assay kit
    Insulin sensitivity, hepatic omega fatty acid composition, and protein markers of stress kinases, lipid peroxidation, oxidative stress, lipid synthesis, and mitochondrial content in control-sedentary (C-Sed), ALA-sedentary (ALA-Sed), control-exercise (C-Ex), or ALA-exercise (ALA-Ex) group obese Zucker rats. AKT phosphorylation ( A ), hepatic n-3 and n-6 polyunsaturated fatty acids (PUFAs) ( B ), markers of mitochondrial content, stress kinases, antioxidants, oxidative stress, and TAG synthesis ( C ) in obese Zucker rats. C, control; EPA, eicosapentaenoic acid; DHA, docosahexaenoic acid; LA, linoleic acid; AA, arachidonic acid; CAT, catalase; SOD, superoxide dismutase; GPAT, <t>glycerol-3-phosphate</t> <t>acyltransferase;</t> DGAT, diacylglyceride transferase; 4HNE, 4-hydroxynonenal; JNK, c-jun NH 2 -terminal kinases; OD, optical density. Data are expressed as means ± SE; n = 5/group. “Main effect” represents Ex greater than Sed or ALA greater than C.
    Amplite Fluorimetric G3p Assay Kit, supplied by AAT Bioquest, used in various techniques. Bioz Stars score: 84/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore anti gapdh antibody
    GLUT12 is required for maximal glucose uptake and cell growth in prostate cancer cells. (A) Indicated prostate cancer cells were transfected with <t>siRNAs</t> targeting a scramble sequence (siControl) or SLC2A12 (siGLUT12). After 72 h, whole cell lysates were extracted and probed for GLUT12 and <t>GAPDH</t> (loading control) using Western blot analysis. (B) Indicated prostate cancer cells were transfected as in Fig. 3A. LNCaP or VCaP cells were also treated for 72 h ± androgen (R1881). Glucose uptake was then measured using a bioanalyzer and data were normalized to cellular DNA content that was measured using a fluorescent DNA stain. *, significant ( P
    Anti Gapdh Antibody, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 6371 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher control gapdh
    GLUT12 is required for maximal glucose uptake and cell growth in prostate cancer cells. (A) Indicated prostate cancer cells were transfected with <t>siRNAs</t> targeting a scramble sequence (siControl) or SLC2A12 (siGLUT12). After 72 h, whole cell lysates were extracted and probed for GLUT12 and <t>GAPDH</t> (loading control) using Western blot analysis. (B) Indicated prostate cancer cells were transfected as in Fig. 3A. LNCaP or VCaP cells were also treated for 72 h ± androgen (R1881). Glucose uptake was then measured using a bioanalyzer and data were normalized to cellular DNA content that was measured using a fluorescent DNA stain. *, significant ( P
    Control Gapdh, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 255 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Cell Signaling Technology Inc rabbit anti gapdh g3p hrp
    Validation of differentially expressed proteins in GT1-7 cells after AAS exposure. (A-E) Representative Western blots of identified proteins from protein extracts of AAS or vehicle-treated cells. (F-J) Densitometry analysis of each protein normalized to β-actin represents the relative protein expression values for (A) Glutathione S-transferase Mu 1 (GSTM1), (B) Glyceraldehyde 3-phosphate dehydrogenase <t>(G3P/GAPDH),</t> (C) Enhancer of rudimentary homolog (ERH), (D) Phosphatidylethanolamine-binding protein 1 (PEBP1), (E) Protein disulfide-isomerase A6/Endoplasmic Reticulum Protein (ERP/PDIA6). Error bars represent standard error of the mean. *p≤0.05, **p≤0.01, unpaired t-test. n = three replicates of three independent experiments for each group.
    Rabbit Anti Gapdh G3p Hrp, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Thermo Fisher mouse gapdh
    Validation of differentially expressed proteins in GT1-7 cells after AAS exposure. (A-E) Representative Western blots of identified proteins from protein extracts of AAS or vehicle-treated cells. (F-J) Densitometry analysis of each protein normalized to β-actin represents the relative protein expression values for (A) Glutathione S-transferase Mu 1 (GSTM1), (B) Glyceraldehyde 3-phosphate dehydrogenase <t>(G3P/GAPDH),</t> (C) Enhancer of rudimentary homolog (ERH), (D) Phosphatidylethanolamine-binding protein 1 (PEBP1), (E) Protein disulfide-isomerase A6/Endoplasmic Reticulum Protein (ERP/PDIA6). Error bars represent standard error of the mean. *p≤0.05, **p≤0.01, unpaired t-test. n = three replicates of three independent experiments for each group.
    Mouse Gapdh, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 674 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Millipore g3p bis salt
    <t>G3P</t>
    G3p Bis Salt, supplied by Millipore, 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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    89
    American Radiolabeled Chemicals Inc g3p
    <t>G3P</t>
    G3p, supplied by American Radiolabeled Chemicals Inc, used in various techniques. Bioz Stars score: 89/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    American Radiolabeled Chemicals Inc h g3p
    <t>G3P</t>
    H G3p, supplied by American Radiolabeled Chemicals Inc, used in various techniques. Bioz Stars score: 85/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Arista Biologicals s canine origin g3p
    <t>G3P</t>
    S Canine Origin G3p, supplied by Arista Biologicals, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate (G3P) and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.

    Journal: Frontiers in Molecular Biosciences

    Article Title: Millisecond Timescale Motions Connect Amino Acid Interaction Networks in Alpha Tryptophan Synthase

    doi: 10.3389/fmolb.2018.00092

    Figure Lengend Snippet: Conformational exchange events in the E.coli αTS enzyme (A) in the apo resting state, (B) bound to product indole, (C) bound to the product glyceraldehyde-3-phosphate (G3P) and (D) in the working state under catalytic turnover. The working ). (left) example 15 N R 2 relaxation dispersion curves collected at a 1 H Larmor frequency of 850 MHz for the resonances belonging to Ala9 (black), Ala18 (green), Ile166 (blue), and Ala198 (purple). (middle) locations of conformational exchange according to the R 2 relaxation dispersion experiments plotted as spheres onto the αTS structure. Here, we used the S.typhimurium αTS structure bound to glyceraldehyde-3-phosphate (PDB 2CLK) as it contains resolved β2α2 and β6α6 loops. Purple spheres indicate that associated R 2 relaxation dispersion curves can be fit to two-site exchange, while pink spheres indicate exchange broadening, but the R 2 relaxation dispersion curves cannot be fit reliably to two-site exchange. (right) a comparison of the conformational exchange events in the resting apo state compared to when αTS is bound with ligands. Blue (red) spheres indicate conformational exchange events present in the apo (ligand-bound) state but not in the ligand-bound (apo) state. Most of the amino acid residues associated with a change in conformational dynamics make contact and/or near each other in three-dimensional space. The R 2 relaxation dispersion experiments were conducted at 283 K using a buffer consisting of 50 mM potassium phosphate, pH 7.8, 2 mM DTT, 0.2 mM Na 2 EDTA, and 10% 2 H 2 O, and 0.5–1.0 mM protein with 10 mM indole and/or 20 mM G3P where appropriate.

    Article Snippet: The samples contained 0.5–1.0 mM protein with 10 mM indole (Thermo Fisher), 20 mM G3P (Sigma Aldrich), and/or 3 mM IGP where appropriate.

    Techniques:

    Insulin sensitivity, hepatic omega fatty acid composition, and protein markers of stress kinases, lipid peroxidation, oxidative stress, lipid synthesis, and mitochondrial content in control-sedentary (C-Sed), ALA-sedentary (ALA-Sed), control-exercise (C-Ex), or ALA-exercise (ALA-Ex) group obese Zucker rats. AKT phosphorylation ( A ), hepatic n-3 and n-6 polyunsaturated fatty acids (PUFAs) ( B ), markers of mitochondrial content, stress kinases, antioxidants, oxidative stress, and TAG synthesis ( C ) in obese Zucker rats. C, control; EPA, eicosapentaenoic acid; DHA, docosahexaenoic acid; LA, linoleic acid; AA, arachidonic acid; CAT, catalase; SOD, superoxide dismutase; GPAT, glycerol-3-phosphate acyltransferase; DGAT, diacylglyceride transferase; 4HNE, 4-hydroxynonenal; JNK, c-jun NH 2 -terminal kinases; OD, optical density. Data are expressed as means ± SE; n = 5/group. “Main effect” represents Ex greater than Sed or ALA greater than C.

    Journal: American Journal of Physiology - Endocrinology and Metabolism

    Article Title: α-Linolenic acid supplementation and exercise training reveal independent and additive responses on hepatic lipid accumulation in obese rats

    doi: 10.1152/ajpendo.00438.2016

    Figure Lengend Snippet: Insulin sensitivity, hepatic omega fatty acid composition, and protein markers of stress kinases, lipid peroxidation, oxidative stress, lipid synthesis, and mitochondrial content in control-sedentary (C-Sed), ALA-sedentary (ALA-Sed), control-exercise (C-Ex), or ALA-exercise (ALA-Ex) group obese Zucker rats. AKT phosphorylation ( A ), hepatic n-3 and n-6 polyunsaturated fatty acids (PUFAs) ( B ), markers of mitochondrial content, stress kinases, antioxidants, oxidative stress, and TAG synthesis ( C ) in obese Zucker rats. C, control; EPA, eicosapentaenoic acid; DHA, docosahexaenoic acid; LA, linoleic acid; AA, arachidonic acid; CAT, catalase; SOD, superoxide dismutase; GPAT, glycerol-3-phosphate acyltransferase; DGAT, diacylglyceride transferase; 4HNE, 4-hydroxynonenal; JNK, c-jun NH 2 -terminal kinases; OD, optical density. Data are expressed as means ± SE; n = 5/group. “Main effect” represents Ex greater than Sed or ALA greater than C.

    Article Snippet: Liver homogenates were diluted (1 μg/μl) and equal amounts of protein (5 μg protein) were loaded for Western blot detection of α-tubulin (Abcam, Cambridge, MA), OXPHOS (Mitoscience, Eugene, OR), total JNK (Cell Signaling), p-JNK (Cell Signaling), total ERK (Cell Signaling), p-ERK(Cell Signaling), catalase (Abcam), SOD2 (Abcam), 4-hydroxynonenal (4HNE; Alpha Diagnostic), oxyblot (Millipore), MTTP (Santa Cruz Biotechnology), diacylglyceride transferase (DGAT; Abcam), glycerol-3-phosphate acyltransferase (GPAT; Abcam), apolipoprotein B100 (Abcam), microsomal triglyceride transfer protein (Santa Cruz Biotechnology), total Akt (Cell Signaling), phospho-Akt ser473 (Cell Signaling), and phospho-Akt thr308 (Cell Signaling).

    Techniques:

    GLUT12 is required for maximal glucose uptake and cell growth in prostate cancer cells. (A) Indicated prostate cancer cells were transfected with siRNAs targeting a scramble sequence (siControl) or SLC2A12 (siGLUT12). After 72 h, whole cell lysates were extracted and probed for GLUT12 and GAPDH (loading control) using Western blot analysis. (B) Indicated prostate cancer cells were transfected as in Fig. 3A. LNCaP or VCaP cells were also treated for 72 h ± androgen (R1881). Glucose uptake was then measured using a bioanalyzer and data were normalized to cellular DNA content that was measured using a fluorescent DNA stain. *, significant ( P

    Journal: Endocrine-related cancer

    Article Title: GLUT12 promotes prostate cancer cell growth and is regulated by androgens and CaMKK2 signaling

    doi: 10.1530/ERC-17-0051

    Figure Lengend Snippet: GLUT12 is required for maximal glucose uptake and cell growth in prostate cancer cells. (A) Indicated prostate cancer cells were transfected with siRNAs targeting a scramble sequence (siControl) or SLC2A12 (siGLUT12). After 72 h, whole cell lysates were extracted and probed for GLUT12 and GAPDH (loading control) using Western blot analysis. (B) Indicated prostate cancer cells were transfected as in Fig. 3A. LNCaP or VCaP cells were also treated for 72 h ± androgen (R1881). Glucose uptake was then measured using a bioanalyzer and data were normalized to cellular DNA content that was measured using a fluorescent DNA stain. *, significant ( P

    Article Snippet: Mission siRNAs targeting SLC2A12 (GLUT12) and TBC1D4 , universal siRNA negative control, and anti-GAPDH antibody were purchased from Sigma-Aldrich (St. Louis, MO, USA).

    Techniques: Transfection, Sequencing, Western Blot, Staining

    Validation of differentially expressed proteins in GT1-7 cells after AAS exposure. (A-E) Representative Western blots of identified proteins from protein extracts of AAS or vehicle-treated cells. (F-J) Densitometry analysis of each protein normalized to β-actin represents the relative protein expression values for (A) Glutathione S-transferase Mu 1 (GSTM1), (B) Glyceraldehyde 3-phosphate dehydrogenase (G3P/GAPDH), (C) Enhancer of rudimentary homolog (ERH), (D) Phosphatidylethanolamine-binding protein 1 (PEBP1), (E) Protein disulfide-isomerase A6/Endoplasmic Reticulum Protein (ERP/PDIA6). Error bars represent standard error of the mean. *p≤0.05, **p≤0.01, unpaired t-test. n = three replicates of three independent experiments for each group.

    Journal: PLoS ONE

    Article Title: Differential protein expression profile in the hypothalamic GT1-7 cell line after exposure to anabolic androgenic steroids

    doi: 10.1371/journal.pone.0180409

    Figure Lengend Snippet: Validation of differentially expressed proteins in GT1-7 cells after AAS exposure. (A-E) Representative Western blots of identified proteins from protein extracts of AAS or vehicle-treated cells. (F-J) Densitometry analysis of each protein normalized to β-actin represents the relative protein expression values for (A) Glutathione S-transferase Mu 1 (GSTM1), (B) Glyceraldehyde 3-phosphate dehydrogenase (G3P/GAPDH), (C) Enhancer of rudimentary homolog (ERH), (D) Phosphatidylethanolamine-binding protein 1 (PEBP1), (E) Protein disulfide-isomerase A6/Endoplasmic Reticulum Protein (ERP/PDIA6). Error bars represent standard error of the mean. *p≤0.05, **p≤0.01, unpaired t-test. n = three replicates of three independent experiments for each group.

    Article Snippet: Antibodies The following primary antibodies were used: mouse anti-ERH (1:1000), mouse anti-PDIA6/ERP (1:1000), rabbit anti-ERα (1:1500), goat anti-AR (1:1000) and rabbit anti-GnRH1 (1:1000) from Santa Cruz Biotechnology (SCBT), Dallas, TX; rabbit anti-GSTM1 (1:2000) from Thermo Scientific, Waltham, MA; rabbit anti-PEBP1/RKIP (1:1000), rabbit anti-GAPDH (G3P)-HRP conjugated (1:3000), rabbit anti-p-ERK (1:10000), rabbit anti-ERK (1:6000), rabbit anti-p-p38 MAPK (Thr180/Tyr182) (1:10000), rabbit anti-AKT (pan) (1:15000) and rabbit anti-β-actin HRP conjugated (1:3000) from Cell Signaling Technology (CST) Danvers, MA.

    Techniques: Atomic Absorption Spectroscopy, Western Blot, Expressing, Binding Assay

    G3P

    Journal: Molecular Plant Pathology

    Article Title: Application of glycerol as a foliar spray activates the defence response and enhances disease resistance of Theobroma cacao

    doi: 10.1111/mpp.12158

    Figure Lengend Snippet: G3P

    Article Snippet: Under these conditions, G3P bis salt (Sigma, Cat. G7886) eluted as a single peak at m / z 171.0063 with a retention time of 7.27 min.

    Techniques:

    G3P

    Journal: Molecular Plant Pathology

    Article Title: Application of glycerol as a foliar spray activates the defence response and enhances disease resistance of Theobroma cacao

    doi: 10.1111/mpp.12158

    Figure Lengend Snippet: G3P

    Article Snippet: Under these conditions, G3P bis salt (Sigma, Cat. G7886) eluted as a single peak at m / z 171.0063 with a retention time of 7.27 min.

    Techniques: