s12 Search Results


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ATCC 15697d 5 jm109 gwbc f2 gift
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ATCC isoptericola variabilis 225
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Delsys Inc neuromap
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Proteintech anti rpn8
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92
Proteintech rps12
(A) Diagram of the WT, Flox and KO alleles of <t>RpS12</t> generated in this study indicating the position of Snord100 and Snora33 (snoRNA),Cas9 gRNAs target locations, and primers used for genotyping. The homology arms starting sites are indicated and the ends fall outside of the RpS12 locus. To identify the first transformants, two pair of primers were used for PCR amplification: F2/R2 and F3/R3. F2 and R3 fall outside of the sequence covered by the homology arms, to ensure the inserts are on the correct location. The presence of LoxP sites was confirmed by Sanger sequencing using primers F1 and F4 for F2/R2 fragments, and with F3 and R3 for F3/R3 fragments. To determine excision of exon 2 and 3 by Cre recombination primers F1 and R1 were used, which generate a 900bp fragment in RpS12 + and a 300bp fragment in RpS12 KO (B) .
Rps12, supplied by Proteintech, 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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Chem Impex International diosgenin
(A) Diagram of the WT, Flox and KO alleles of <t>RpS12</t> generated in this study indicating the position of Snord100 and Snora33 (snoRNA),Cas9 gRNAs target locations, and primers used for genotyping. The homology arms starting sites are indicated and the ends fall outside of the RpS12 locus. To identify the first transformants, two pair of primers were used for PCR amplification: F2/R2 and F3/R3. F2 and R3 fall outside of the sequence covered by the homology arms, to ensure the inserts are on the correct location. The presence of LoxP sites was confirmed by Sanger sequencing using primers F1 and F4 for F2/R2 fragments, and with F3 and R3 for F3/R3 fragments. To determine excision of exon 2 and 3 by Cre recombination primers F1 and R1 were used, which generate a 900bp fragment in RpS12 + and a 300bp fragment in RpS12 KO (B) .
Diosgenin, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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88
Bio-Rad uno s12 column
(A) Diagram of the WT, Flox and KO alleles of <t>RpS12</t> generated in this study indicating the position of Snord100 and Snora33 (snoRNA),Cas9 gRNAs target locations, and primers used for genotyping. The homology arms starting sites are indicated and the ends fall outside of the RpS12 locus. To identify the first transformants, two pair of primers were used for PCR amplification: F2/R2 and F3/R3. F2 and R3 fall outside of the sequence covered by the homology arms, to ensure the inserts are on the correct location. The presence of LoxP sites was confirmed by Sanger sequencing using primers F1 and F4 for F2/R2 fragments, and with F3 and R3 for F3/R3 fragments. To determine excision of exon 2 and 3 by Cre recombination primers F1 and R1 were used, which generate a 900bp fragment in RpS12 + and a 300bp fragment in RpS12 KO (B) .
Uno S12 Column, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
Sino Biological sik3
(A) Diagram of the WT, Flox and KO alleles of <t>RpS12</t> generated in this study indicating the position of Snord100 and Snora33 (snoRNA),Cas9 gRNAs target locations, and primers used for genotyping. The homology arms starting sites are indicated and the ends fall outside of the RpS12 locus. To identify the first transformants, two pair of primers were used for PCR amplification: F2/R2 and F3/R3. F2 and R3 fall outside of the sequence covered by the homology arms, to ensure the inserts are on the correct location. The presence of LoxP sites was confirmed by Sanger sequencing using primers F1 and F4 for F2/R2 fragments, and with F3 and R3 for F3/R3 fragments. To determine excision of exon 2 and 3 by Cre recombination primers F1 and R1 were used, which generate a 900bp fragment in RpS12 + and a 300bp fragment in RpS12 KO (B) .
Sik3, supplied by Sino Biological, 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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MedChemExpress zinc000012495776 ltb4 ethanol amide
Top 20 ranked compounds with higher libdock scores than Rapamycin.
Zinc000012495776 Ltb4 Ethanol Amide, supplied by MedChemExpress, 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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Addgene inc pcrispr s12 based vectors
Top 20 ranked compounds with higher libdock scores than Rapamycin.
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ATCC fimicarius atcc21900 streptomyces
Top 20 ranked compounds with higher libdock scores than Rapamycin.
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Proteintech rabbit polyclonal

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Image Search Results


(A) Diagram of the WT, Flox and KO alleles of RpS12 generated in this study indicating the position of Snord100 and Snora33 (snoRNA),Cas9 gRNAs target locations, and primers used for genotyping. The homology arms starting sites are indicated and the ends fall outside of the RpS12 locus. To identify the first transformants, two pair of primers were used for PCR amplification: F2/R2 and F3/R3. F2 and R3 fall outside of the sequence covered by the homology arms, to ensure the inserts are on the correct location. The presence of LoxP sites was confirmed by Sanger sequencing using primers F1 and F4 for F2/R2 fragments, and with F3 and R3 for F3/R3 fragments. To determine excision of exon 2 and 3 by Cre recombination primers F1 and R1 were used, which generate a 900bp fragment in RpS12 + and a 300bp fragment in RpS12 KO (B) .

Journal: bioRxiv

Article Title: Haploinsufficiency of the essential gene RpS12 causes defects in erythropoiesis and hematopoietic stem cell maintenance

doi: 10.1101/2021.05.04.442585

Figure Lengend Snippet: (A) Diagram of the WT, Flox and KO alleles of RpS12 generated in this study indicating the position of Snord100 and Snora33 (snoRNA),Cas9 gRNAs target locations, and primers used for genotyping. The homology arms starting sites are indicated and the ends fall outside of the RpS12 locus. To identify the first transformants, two pair of primers were used for PCR amplification: F2/R2 and F3/R3. F2 and R3 fall outside of the sequence covered by the homology arms, to ensure the inserts are on the correct location. The presence of LoxP sites was confirmed by Sanger sequencing using primers F1 and F4 for F2/R2 fragments, and with F3 and R3 for F3/R3 fragments. To determine excision of exon 2 and 3 by Cre recombination primers F1 and R1 were used, which generate a 900bp fragment in RpS12 + and a 300bp fragment in RpS12 KO (B) .

Article Snippet: The following primary antibodies were used: RpS12 (Proteintech; polyclonal), β-actin (Cell Signaling; 13E5), eIF2α (Cell signaling, 5324T), phospho-eIF2α (Thermo Scientific; Ser52; polyclonal).

Techniques: Generated, Amplification, Sequencing

(A) Conditional RpS12 flox transgenic knock-in has two loxP sites flanking exons 2 and 3, that are removed by Cre recombinase activity to generate RpS12 KO . (B) Post-natal growth curve of RpS12 KO/+ and RpS12 +/+ littermates (+/+ n=8 and KO/+ n=11 pups). (C) Picture of 5-day-old RpS12 KO/+ and RpS12 +/+ littermates. (D) Representative picture of “kinked” tail in RpS12 KO/+ mouse. (E) Representative picture of the anterior footpad hyperpigmentation in RpS12 KO/+ . (F) Quantification of the percentage of mice presenting hydrocephalus per litter (n=27 litters, 2-way ANOVA p=0.0035). (G) Kaplan-Meier survival curves of RpS12 KO/+ and RpS12 +/+ littermates starting at day 5 of age (+/+ n=39 and KO/+ n=60, log-rank Mantel-Cox test p=0.012). (H) Embryo genotype segregation from crosses between RpS12 KO/+ male and female. Graph represents percentage of developed embryos and the table shows the total numbers (E%=expected percentages, E#=expected numbers, O=observed numbers). (I) Representative pictures of E13.5 embryos with their placentas. (J) E13.5 embryo weights (n=10 on each genotype, unpaired t-test p=0.0420).

Journal: bioRxiv

Article Title: Haploinsufficiency of the essential gene RpS12 causes defects in erythropoiesis and hematopoietic stem cell maintenance

doi: 10.1101/2021.05.04.442585

Figure Lengend Snippet: (A) Conditional RpS12 flox transgenic knock-in has two loxP sites flanking exons 2 and 3, that are removed by Cre recombinase activity to generate RpS12 KO . (B) Post-natal growth curve of RpS12 KO/+ and RpS12 +/+ littermates (+/+ n=8 and KO/+ n=11 pups). (C) Picture of 5-day-old RpS12 KO/+ and RpS12 +/+ littermates. (D) Representative picture of “kinked” tail in RpS12 KO/+ mouse. (E) Representative picture of the anterior footpad hyperpigmentation in RpS12 KO/+ . (F) Quantification of the percentage of mice presenting hydrocephalus per litter (n=27 litters, 2-way ANOVA p=0.0035). (G) Kaplan-Meier survival curves of RpS12 KO/+ and RpS12 +/+ littermates starting at day 5 of age (+/+ n=39 and KO/+ n=60, log-rank Mantel-Cox test p=0.012). (H) Embryo genotype segregation from crosses between RpS12 KO/+ male and female. Graph represents percentage of developed embryos and the table shows the total numbers (E%=expected percentages, E#=expected numbers, O=observed numbers). (I) Representative pictures of E13.5 embryos with their placentas. (J) E13.5 embryo weights (n=10 on each genotype, unpaired t-test p=0.0420).

Article Snippet: The following primary antibodies were used: RpS12 (Proteintech; polyclonal), β-actin (Cell Signaling; 13E5), eIF2α (Cell signaling, 5324T), phospho-eIF2α (Thermo Scientific; Ser52; polyclonal).

Techniques: Transgenic Assay, Knock-In, Activity Assay

(A) Non-competitive BM transplant strategy testing the long-term reconstituting activity of RpS12 KO/+ HSCs. 10 6 bone marrow cells from RpS12 KO/+ or RpS12 flox/flox samples (CD45.2+) were transplanted into lethally irradiated B6.SJL (CD45.1+) mice, peripheral blood chimerism was determined every 4 weeks. (B) Kaplan-Meier survival curves of mice transplanted with BM cells from RpS12 KO/+ and control RpS12 flox/+ or RpS12 flox/flox mice (control n=20 and KO/+ n=20 transplanted mice, combination of 2 independent non-competitive transplants with 1 donor per genotype transplanted into 10 host mice each). (C) Frequency of recipient mice with long-term (20-weeks) multi-lineage reconstitution (≥0.5% in all three macrophages, B, and T cells)(control n=20 and KO/+ n=20 transplanted mice, combination of 2 independent non-competitive transplants). (D-G) Peripheral blood donor derived (D) total chimerism and (E-G) multi-lineage chimerism in non-competitively transplanted whole bone marrow (CD45.2+) recipients (flox/flox n=10 and KO/+ n=10). (H) Schematic representation of the competitive bone marrow transplant. 5×10 5 cells from RpS12 KO/+ or RpS12 flox/+ donor bone marrow (CD45.2+) mixed with 5×10 5 competitor bone marrow cells from B6.SJL (CD45.1+) mice were injected into lethally irradiated B6.SJL (CD45.1+) mice. Chimerism in peripheral blood was determined every 4 weeks and bone marrow chimerism was analyzed at 20 weeks after transplant. (I) Total bone marrow chimerism and (J) HSCs donor-derived (CD45.2+) chimerism in the recipient bone marrow (Flox/+ n=10 and KO/+ n=10 competitive-transplanted mice). (K-N) Donor derived peripheral blood chimerism of competitively transplanted RpS12 KO/+ or RpS12 flox/+ bone marrow cells as described in H . Non-competitive transplants were performed twice, using different controls: RpS12 flox/+ or RpS12 flox/flox . The competitive transplant was performed once, using RpS12 flox/+ mice as a control group Statistical analysis: data represent mean +/-SEM, unpaired t-tests were performed to assess significance among populations between genotypes *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001

Journal: bioRxiv

Article Title: Haploinsufficiency of the essential gene RpS12 causes defects in erythropoiesis and hematopoietic stem cell maintenance

doi: 10.1101/2021.05.04.442585

Figure Lengend Snippet: (A) Non-competitive BM transplant strategy testing the long-term reconstituting activity of RpS12 KO/+ HSCs. 10 6 bone marrow cells from RpS12 KO/+ or RpS12 flox/flox samples (CD45.2+) were transplanted into lethally irradiated B6.SJL (CD45.1+) mice, peripheral blood chimerism was determined every 4 weeks. (B) Kaplan-Meier survival curves of mice transplanted with BM cells from RpS12 KO/+ and control RpS12 flox/+ or RpS12 flox/flox mice (control n=20 and KO/+ n=20 transplanted mice, combination of 2 independent non-competitive transplants with 1 donor per genotype transplanted into 10 host mice each). (C) Frequency of recipient mice with long-term (20-weeks) multi-lineage reconstitution (≥0.5% in all three macrophages, B, and T cells)(control n=20 and KO/+ n=20 transplanted mice, combination of 2 independent non-competitive transplants). (D-G) Peripheral blood donor derived (D) total chimerism and (E-G) multi-lineage chimerism in non-competitively transplanted whole bone marrow (CD45.2+) recipients (flox/flox n=10 and KO/+ n=10). (H) Schematic representation of the competitive bone marrow transplant. 5×10 5 cells from RpS12 KO/+ or RpS12 flox/+ donor bone marrow (CD45.2+) mixed with 5×10 5 competitor bone marrow cells from B6.SJL (CD45.1+) mice were injected into lethally irradiated B6.SJL (CD45.1+) mice. Chimerism in peripheral blood was determined every 4 weeks and bone marrow chimerism was analyzed at 20 weeks after transplant. (I) Total bone marrow chimerism and (J) HSCs donor-derived (CD45.2+) chimerism in the recipient bone marrow (Flox/+ n=10 and KO/+ n=10 competitive-transplanted mice). (K-N) Donor derived peripheral blood chimerism of competitively transplanted RpS12 KO/+ or RpS12 flox/+ bone marrow cells as described in H . Non-competitive transplants were performed twice, using different controls: RpS12 flox/+ or RpS12 flox/flox . The competitive transplant was performed once, using RpS12 flox/+ mice as a control group Statistical analysis: data represent mean +/-SEM, unpaired t-tests were performed to assess significance among populations between genotypes *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001

Article Snippet: The following primary antibodies were used: RpS12 (Proteintech; polyclonal), β-actin (Cell Signaling; 13E5), eIF2α (Cell signaling, 5324T), phospho-eIF2α (Thermo Scientific; Ser52; polyclonal).

Techniques: Activity Assay, Irradiation, Control, Derivative Assay, Injection

(A) Representative images of RpS12 +/- and littermate E13.5 fetal livers. (B) Quantification of total number of cells per liver, normalized to embryo weight (+/+ n=9 and KO/+ n=8). (C) Representative flow cytometry gating of erythropoietic populations using Ter119 and CD71 markers of fetal liver samples from E13.5 embryos. (E) Representative flow cytometry gating of Lin- (top) and LSK (bottom) populations in E13.5 fetal livers. (F,G,H) LT-HSCs, ST-HSCs and indicated progenitor populations represented as percentages of the Lin- population in E13.5 fetal livers. (D,F,G,H) Biological samples are +/+ n=8 and KO/+ n=4. Statistical analysis: quantifications represent mean +/-SEM, unpaired t-tests were performed to established significance among populations between genotypes *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001

Journal: bioRxiv

Article Title: Haploinsufficiency of the essential gene RpS12 causes defects in erythropoiesis and hematopoietic stem cell maintenance

doi: 10.1101/2021.05.04.442585

Figure Lengend Snippet: (A) Representative images of RpS12 +/- and littermate E13.5 fetal livers. (B) Quantification of total number of cells per liver, normalized to embryo weight (+/+ n=9 and KO/+ n=8). (C) Representative flow cytometry gating of erythropoietic populations using Ter119 and CD71 markers of fetal liver samples from E13.5 embryos. (E) Representative flow cytometry gating of Lin- (top) and LSK (bottom) populations in E13.5 fetal livers. (F,G,H) LT-HSCs, ST-HSCs and indicated progenitor populations represented as percentages of the Lin- population in E13.5 fetal livers. (D,F,G,H) Biological samples are +/+ n=8 and KO/+ n=4. Statistical analysis: quantifications represent mean +/-SEM, unpaired t-tests were performed to established significance among populations between genotypes *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001

Article Snippet: The following primary antibodies were used: RpS12 (Proteintech; polyclonal), β-actin (Cell Signaling; 13E5), eIF2α (Cell signaling, 5324T), phospho-eIF2α (Thermo Scientific; Ser52; polyclonal).

Techniques: Flow Cytometry

(A) Representative flow cytometry gating of HSCs (Flk2 - CD48 - LSK) cell cycle stages (G0, G1, S/G2/M) distribution determined by DNA (Hoechst) and Ki67 levels. (B) Cell cycle stages distribution in HSCs and in indicated progenitor populations. Asterisks correspond to p values assessing significant differences in each cell cycle stage between RpS12 KO/+ and RpS12 +/+ mice (6-8-weeks-old littermates, +/+ n=4 and KO/+ n=3). (C) Representative flow cytometry histogram showing OPP intensity in RpS12 KO/+ (green) and RpS12 +/+ (grey) HSCs. (D, E) Median OPP intensity of the indicated bone marrow populations (6-8-weeks-old littermates, +/+ n=4 and KO/+ n=3). This analysis was repeated in 6-7-month-old mice with similar results. (F) Representative images of bone marrow cytospins showing high number of apoptotic cells (arrows) in RpS12 KO/+ samples. (G) Representative flow cytometry gating of LIN- population showing apoptotic populations as determined by AnexinV and PI staining. (H, I) Percentage of apoptotic (AnnexinV+) cells in LSK (Lin - cKit + Sca1 + ) and Myeloid progenitor (MPROG; Lin - cKit + Sca1 - ) populations (6-8-weeks-old littermates, +/+ n=4 and KO/+ n=3). Statistical analysis: quantifications represent mean+/-SEM, two-way ANOVA (B-F) and unpaired t-tests were performed to established significance among populations between genotypes *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001

Journal: bioRxiv

Article Title: Haploinsufficiency of the essential gene RpS12 causes defects in erythropoiesis and hematopoietic stem cell maintenance

doi: 10.1101/2021.05.04.442585

Figure Lengend Snippet: (A) Representative flow cytometry gating of HSCs (Flk2 - CD48 - LSK) cell cycle stages (G0, G1, S/G2/M) distribution determined by DNA (Hoechst) and Ki67 levels. (B) Cell cycle stages distribution in HSCs and in indicated progenitor populations. Asterisks correspond to p values assessing significant differences in each cell cycle stage between RpS12 KO/+ and RpS12 +/+ mice (6-8-weeks-old littermates, +/+ n=4 and KO/+ n=3). (C) Representative flow cytometry histogram showing OPP intensity in RpS12 KO/+ (green) and RpS12 +/+ (grey) HSCs. (D, E) Median OPP intensity of the indicated bone marrow populations (6-8-weeks-old littermates, +/+ n=4 and KO/+ n=3). This analysis was repeated in 6-7-month-old mice with similar results. (F) Representative images of bone marrow cytospins showing high number of apoptotic cells (arrows) in RpS12 KO/+ samples. (G) Representative flow cytometry gating of LIN- population showing apoptotic populations as determined by AnexinV and PI staining. (H, I) Percentage of apoptotic (AnnexinV+) cells in LSK (Lin - cKit + Sca1 + ) and Myeloid progenitor (MPROG; Lin - cKit + Sca1 - ) populations (6-8-weeks-old littermates, +/+ n=4 and KO/+ n=3). Statistical analysis: quantifications represent mean+/-SEM, two-way ANOVA (B-F) and unpaired t-tests were performed to established significance among populations between genotypes *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001

Article Snippet: The following primary antibodies were used: RpS12 (Proteintech; polyclonal), β-actin (Cell Signaling; 13E5), eIF2α (Cell signaling, 5324T), phospho-eIF2α (Thermo Scientific; Ser52; polyclonal).

Techniques: Flow Cytometry, Staining

Top 20 ranked compounds with higher libdock scores than Rapamycin.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: Top 20 ranked compounds with higher libdock scores than Rapamycin.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques:

ADME (Adsorption, Distribution, Metabolism, Excretion) properties of compounds.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: ADME (Adsorption, Distribution, Metabolism, Excretion) properties of compounds.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques: Adsorption, Solubility

Toxicities of compounds.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: Toxicities of compounds.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques:

The structures of Rapamycin and novel compounds selected from virtual screening. ( A ) ZINC000013374324; ( B ) ZINC000012495776; ( C ) Rapamycin.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: The structures of Rapamycin and novel compounds selected from virtual screening. ( A ) ZINC000013374324; ( B ) ZINC000012495776; ( C ) Rapamycin.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques:

CDOCKER interaction energy of compounds with mTORC1.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: CDOCKER interaction energy of compounds with mTORC1.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques:

Hydrogen bond interaction parameters for each compound and mTORC1 residues.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: Hydrogen bond interaction parameters for each compound and mTORC1 residues.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques:

( A ) ZINC000013374324-mTORC1 complex. Schematic drawing of interactions between ligands and mTORC1, the surface of the binding area was added, blue represented positive charge, red represented negative charge, and ligands were shown in the sticks, the structure around the ligand-receptor junction was shown in thinner sticks. ( B ) ZINC000012495776 -mTORC1 complex. Schematic drawing of interactions between ligands and mTORC1, the surface of the binding area was added, blue represented positive charge, red represented negative charge, and ligands were shown in the sticks, the structure around the ligand-receptor junction was shown in thinner sticks. ( C ) Rapamycin-mTORC1 complex. Schematic drawing of interactions between ligands and mTORC1, the surface of the binding area was added, blue represented positive charge, red represented negative charge, and ligands were shown in the sticks, the structure around the ligand-receptor junction was shown in thinner sticks.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: ( A ) ZINC000013374324-mTORC1 complex. Schematic drawing of interactions between ligands and mTORC1, the surface of the binding area was added, blue represented positive charge, red represented negative charge, and ligands were shown in the sticks, the structure around the ligand-receptor junction was shown in thinner sticks. ( B ) ZINC000012495776 -mTORC1 complex. Schematic drawing of interactions between ligands and mTORC1, the surface of the binding area was added, blue represented positive charge, red represented negative charge, and ligands were shown in the sticks, the structure around the ligand-receptor junction was shown in thinner sticks. ( C ) Rapamycin-mTORC1 complex. Schematic drawing of interactions between ligands and mTORC1, the surface of the binding area was added, blue represented positive charge, red represented negative charge, and ligands were shown in the sticks, the structure around the ligand-receptor junction was shown in thinner sticks.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques: Binding Assay

The inter-molecular interaction of the predicted binding modes of ( A ) ZINC000013374324 to mTORC1; ( B ) ZINC000012495776 to mTORC1.; ( C ) Rapamycin to mTORC1.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: The inter-molecular interaction of the predicted binding modes of ( A ) ZINC000013374324 to mTORC1; ( B ) ZINC000012495776 to mTORC1.; ( C ) Rapamycin to mTORC1.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques: Binding Assay

Pi-Sigma interaction, Pi-Pi interaction, Pi-Alkyl interaction and Alkyl interaction parameters for each compound and mTORC1 residues.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: Pi-Sigma interaction, Pi-Pi interaction, Pi-Alkyl interaction and Alkyl interaction parameters for each compound and mTORC1 residues.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques:

The molecular docking by Schrodinger. Ligands were docked into the defined binding pocket. Red represents positive charge; blue represents negative charge. ( A ) ZINC000013374324 to mTORC1; ( B ) ZINC000012495776 to mTORC1.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: The molecular docking by Schrodinger. Ligands were docked into the defined binding pocket. Red represents positive charge; blue represents negative charge. ( A ) ZINC000013374324 to mTORC1; ( B ) ZINC000012495776 to mTORC1.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques: Binding Assay

The inter-molecular interaction by Schrodinger of the predicted binding modes of ( A ) ZINC000013374324 to mTORC1; ( B ) ZINC000012495776 to mTORC1.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: The inter-molecular interaction by Schrodinger of the predicted binding modes of ( A ) ZINC000013374324 to mTORC1; ( B ) ZINC000012495776 to mTORC1.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques: Binding Assay

Pharmacophore predictions using Schrodinger. Red represents hydrogen acceptor; blue represents hydrogen donor, green represents the hydrophobic center, and yellow represents Aromatic Ring. ( A ) ZINC000013374324 to mTORC1; ( B ) ZINC000012495776 to mTORC1.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: Pharmacophore predictions using Schrodinger. Red represents hydrogen acceptor; blue represents hydrogen donor, green represents the hydrophobic center, and yellow represents Aromatic Ring. ( A ) ZINC000013374324 to mTORC1; ( B ) ZINC000012495776 to mTORC1.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques:

The establishment of an enzymatic reaction system of different concentrations of selected molecules and the determination of mTOR protein activity. ( A ) Aurantiamide Acetate; ( B ) Ltb4 Ethanol Amide.

Journal: Aging (Albany NY)

Article Title: Computational research of mTORC1 inhibitor on cerebral ischemia-reperfusion injury

doi: 10.18632/aging.203371

Figure Lengend Snippet: The establishment of an enzymatic reaction system of different concentrations of selected molecules and the determination of mTOR protein activity. ( A ) Aurantiamide Acetate; ( B ) Ltb4 Ethanol Amide.

Article Snippet: mTOR protein (bought from Wuhan Huamei Biological Company), Atg13 (bought from Shanghai Kemin Biological Technology Co., Ltd.), ZINC000013374324: Aurantiamide Acetate (CAS No.: 56121-42-7; bought from MedChemExpress) and ZINC000012495776: Ltb4 Ethanol Amide (CAS No.: 877459-63-7; bought from Good Laboratory Practice Bioscience).

Techniques: Activity Assay

Journal: eLife

Article Title: Haploinsufficiency of the essential gene Rps12 causes defects in erythropoiesis and hematopoietic stem cell maintenance

doi: 10.7554/eLife.69322

Figure Lengend Snippet:

Article Snippet: Antibody , RpS12, rabbit polyclonal , Proteintech , Cat # 16490–1-AP , 1:1000.

Techniques: Generated, Staining, Sequencing, DNA Extraction, Western Blot, Isolation, SYBR Green Assay