17 aag Search Results


(hy-10211)  (MedChemExpress)
95
MedChemExpress (hy-10211)
(Hy 10211), supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/(hy-10211)/product/MedChemExpress
Average 95 stars, based on 1 article reviews
(hy-10211) - by Bioz Stars, 2026-04
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17 allylamino 17 demethoxygeldanamycin  (Alomone Labs)
92
Alomone Labs 17 allylamino 17 demethoxygeldanamycin
17 Allylamino 17 Demethoxygeldanamycin, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
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erbb signaling pathway epithelial cell signaling  (Cell Signaling Technology Inc)
92
Cell Signaling Technology Inc erbb signaling pathway epithelial cell signaling
Pairs of pathway interactions from 2 different drugs with the greatest DCSC score.
Erbb Signaling Pathway Epithelial Cell Signaling, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/erbb signaling pathway epithelial cell signaling/product/Cell Signaling Technology Inc
Average 92 stars, based on 1 article reviews
erbb signaling pathway epithelial cell signaling - by Bioz Stars, 2026-04
92/100 stars
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aag  (Tocris)
91
Tocris aag
Pairs of pathway interactions from 2 different drugs with the greatest DCSC score.
Aag, supplied by Tocris, 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/result/aag/product/Tocris
Average 91 stars, based on 1 article reviews
aag - by Bioz Stars, 2026-04
91/100 stars
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hsp90 inhibitor  (Tocris)
92
Tocris hsp90 inhibitor
(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or <t>Hsp90</t> inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).
Hsp90 Inhibitor, supplied by Tocris, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
hsp90 inhibitor - by Bioz Stars, 2026-04
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aag  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology aag
(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or <t>Hsp90</t> inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).
Aag, supplied by Santa Cruz Biotechnology, 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/aag/product/Santa Cruz Biotechnology
Average 93 stars, based on 1 article reviews
aag - by Bioz Stars, 2026-04
93/100 stars
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peptides  (BOC Sciences)
90
BOC Sciences peptides
(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or <t>Hsp90</t> inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).
Peptides, supplied by BOC Sciences, 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
peptides - by Bioz Stars, 2026-04
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antibodies hsp90 inhibitor 17 aag  (TargetMol)
93
TargetMol antibodies hsp90 inhibitor 17 aag
(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or <t>Hsp90</t> inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).
Antibodies Hsp90 Inhibitor 17 Aag, supplied by TargetMol, 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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antibodies hsp90 inhibitor 17 aag - by Bioz Stars, 2026-04
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17aag  (StressMarq)
90
StressMarq 17aag
(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or <t>Hsp90</t> inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).
17aag, supplied by StressMarq, 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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hsp90 inhibitor 17 allylamino 17 demethoxygeldanamycin  (Alomone Labs)
93
Alomone Labs hsp90 inhibitor 17 allylamino 17 demethoxygeldanamycin
(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or <t>Hsp90</t> inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).
Hsp90 Inhibitor 17 Allylamino 17 Demethoxygeldanamycin, supplied by Alomone Labs, 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
hsp90 inhibitor 17 allylamino 17 demethoxygeldanamycin - by Bioz Stars, 2026-04
93/100 stars
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17-aag  (AG Scientific)
90
AG Scientific 17-aag
(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or <t>Hsp90</t> inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).
17 Aag, supplied by AG Scientific, 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/result/17-aag/product/AG Scientific
Average 90 stars, based on 1 article reviews
17-aag - by Bioz Stars, 2026-04
90/100 stars
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17-aag  (Bristol Myers)
90
Bristol Myers 17-aag
(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or <t>Hsp90</t> inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).
17 Aag, supplied by Bristol Myers, 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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Image Search Results


Pairs of pathway interactions from 2 different drugs with the greatest DCSC score.

Journal: Cancer Informatics

Article Title: Pathway Interactions Based on Drug-Induced Datasets

doi: 10.1177/1176935119851518

Figure Lengend Snippet: Pairs of pathway interactions from 2 different drugs with the greatest DCSC score.

Article Snippet: 17-AAG_wort , 3/1 , ERBB SIGNALING PATHWAY/EPITHELIAL CELL SIGNALING IN HELICOBACTER PYLORI INFECTION , 3.94 , 6.

Techniques: Infection

Interactions of drugs, pathways, and diseases in our and previous studies. (A) Red arrows present the drug to cancer pathway via MTOR as in Chiu et al. (B) Blue arrows present sirolimus to pancreatic cancer pathways via MTOR and ERBB as in Hynes and MacDonald. (C) The ERBB signaling pathway is the primary choice for the breast cancer treatment. – (D) Description of our findings (black arrows) compared with previous studies.

Journal: Cancer Informatics

Article Title: Pathway Interactions Based on Drug-Induced Datasets

doi: 10.1177/1176935119851518

Figure Lengend Snippet: Interactions of drugs, pathways, and diseases in our and previous studies. (A) Red arrows present the drug to cancer pathway via MTOR as in Chiu et al. (B) Blue arrows present sirolimus to pancreatic cancer pathways via MTOR and ERBB as in Hynes and MacDonald. (C) The ERBB signaling pathway is the primary choice for the breast cancer treatment. – (D) Description of our findings (black arrows) compared with previous studies.

Article Snippet: 17-AAG_wort , 3/1 , ERBB SIGNALING PATHWAY/EPITHELIAL CELL SIGNALING IN HELICOBACTER PYLORI INFECTION , 3.94 , 6.

Techniques:

(a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or Hsp90 inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).

Journal: Translational stroke research

Article Title: Ischemic neuroprotectant PKCε restores mitochondrial glutamate oxaloacetate transaminase in the neuronal NADH shuttle after ischemic injury

doi: 10.1007/s12975-019-00729-4

Figure Lengend Snippet: (a) Western blot reveals enriched GOT1 in the cytosolic fraction and GOT2 in the mitochondrial fraction. (b) Primary neurons were exposed to TAT or ΨεRACK (500 nM) for 1 hour. Forty-eight hours later, activity of GOT2 (GOT in the mitochondrial fraction) was measured using Biovision AST colorimetric assay kit and normalized to protein concentration. Values are shown as fold-change of TAT control. (c, d) Neurons were treated with 500 nM vehicle (DMSO) or Hsp90 inhibitor (17-AAG) in the presence of ΨεRACK (500 nM). (c) Representative Western blot for serine-phosphorylation of GOT2. Input-GOT2 acts as a loading control. Quantification fold change of TAT control as shown above. (d) Activity of GOT2 is represented as fold change of control (n=5–7, mean ± SEM, * P <0.05, ns = non-significant, Two-tailed unpaired Student’s t-test).

Article Snippet: For PKCε activation, cells were exposed for 1 hour to 500 nM of control peptide TAT (Sigma, St. Louis, MO), specific PKCε activator TAT-conjugated ΨεRACK (CPC scientific, Sunnyvale, CA), with or without 500 nM Hsp90 inhibitor, 17-AAG (Tocris, Bristol, UK).

Techniques: Western Blot, Activity Assay, Colorimetric Assay, Protein Concentration, Control, Phospho-proteomics, Two Tailed Test