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ptp1b in 4 (MedChemExpress)

Name: ptp1b in 4
Brand: MedChemExpress
Rating: 94 (5 reviews)

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MedChemExpress ptp1b in 4

(A) Single WT and RHOA-KO HEK293 cells were seeded in Geltrex and monitored for 12 days in the presence of 30 μM <t>PTP1B-IN-4.</t> The culture medium containing PTP1B-IN-4 was replaced every 4 days. Scale bar, 50 μm. (B) Quantification of inverse circularity (mean ± SD, n = 3 experiments). (C) Wound-healing assay was performed in the presence of 30 μM PTP1B-IN-4 using WT and RHOA-KO HEK293 cells. Scale bar, 400 μm. (D) Quantification of wound closure (relative wound width over initial width, mean ± SD, n = 3 experiments). Statistical analysis: one-way ANOVA with post hoc Tukey (B and C): * p < 0.05.

Ptp1b In 4, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 5 article reviews

ptp1b in 4 - by Bioz Stars, 2026-03

94/100 stars

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1) Product Images from "Context-dependent inhibitory roles of RhoA in 3D invasive cell migration within the extracellular matrix"

Article Title: Context-dependent inhibitory roles of RhoA in 3D invasive cell migration within the extracellular matrix

Journal: Cell reports

doi: 10.1016/j.celrep.2025.116649

(A) Single WT and RHOA-KO HEK293 cells were seeded in Geltrex and monitored for 12 days in the presence of 30 μM PTP1B-IN-4. The culture medium containing PTP1B-IN-4 was replaced every 4 days. Scale bar, 50 μm. (B) Quantification of inverse circularity (mean ± SD, n = 3 experiments). (C) Wound-healing assay was performed in the presence of 30 μM PTP1B-IN-4 using WT and RHOA-KO HEK293 cells. Scale bar, 400 μm. (D) Quantification of wound closure (relative wound width over initial width, mean ± SD, n = 3 experiments). Statistical analysis: one-way ANOVA with post hoc Tukey (B and C): * p < 0.05.

Figure Legend Snippet: (A) Single WT and RHOA-KO HEK293 cells were seeded in Geltrex and monitored for 12 days in the presence of 30 μM PTP1B-IN-4. The culture medium containing PTP1B-IN-4 was replaced every 4 days. Scale bar, 50 μm. (B) Quantification of inverse circularity (mean ± SD, n = 3 experiments). (C) Wound-healing assay was performed in the presence of 30 μM PTP1B-IN-4 using WT and RHOA-KO HEK293 cells. Scale bar, 400 μm. (D) Quantification of wound closure (relative wound width over initial width, mean ± SD, n = 3 experiments). Statistical analysis: one-way ANOVA with post hoc Tukey (B and C): * p < 0.05.

Techniques Used: Wound Healing Assay

Image Search Results

a Serum zinc concentration in mice 4 weeks after irradiation with administration of TPO or vehicle ( n = 6 per group). b Representative fluozin-3 images and quantitative analysis of LepR + SSCs, with or without MKs, after irradiation ( n = 6 per group). c Representative immunostaining images of Slc39a14 (green) in LepR + SSCs, with or without MKs, after irradiation ( n = 6 per group). Scale bar, 100 µm. d KEGG enrichment analysis of upregulated pathways in LepR + SSCs after irradiation. e GO enrichment analysis of downregulated functions in LepR + SSCs after co-culture with MKs. The top ten enriched GO terms ( P < 0.05) are shown. f Western blotting analysis of the expression of Slc39a14, PTP1B, p-eIF2α, ATF4 and CHOP in LepR + SSCs after co-culture with MKs ( n = 3 per group). g Representative immunostaining images of CHOP (green) in LepR + SSCs, with or without MKs, after irradiation ( n = 6 per group). Scale bar, 100 µm. h Transmission electron microscopy images of LepR + SSCs after irradiation co-culture with MKs ( n = 3 per group). Data on graphs are shown as mean ± SD. One-way ANOVA was used to analyze the data in a – d and g . * P < 0.05, ** P < 0.01 and *** P < 0.001. For all panels in this figure, data are representative of three independent experiments.

Journal: Experimental & Molecular Medicine

Article Title: Megakaryocytic TGFβ1 orchestrates osteogenesis of LepR + SSCs to alleviate radiation-induced bone loss

doi: 10.1038/s12276-025-01612-z

Figure Lengend Snippet: a Serum zinc concentration in mice 4 weeks after irradiation with administration of TPO or vehicle ( n = 6 per group). b Representative fluozin-3 images and quantitative analysis of LepR + SSCs, with or without MKs, after irradiation ( n = 6 per group). c Representative immunostaining images of Slc39a14 (green) in LepR + SSCs, with or without MKs, after irradiation ( n = 6 per group). Scale bar, 100 µm. d KEGG enrichment analysis of upregulated pathways in LepR + SSCs after irradiation. e GO enrichment analysis of downregulated functions in LepR + SSCs after co-culture with MKs. The top ten enriched GO terms ( P < 0.05) are shown. f Western blotting analysis of the expression of Slc39a14, PTP1B, p-eIF2α, ATF4 and CHOP in LepR + SSCs after co-culture with MKs ( n = 3 per group). g Representative immunostaining images of CHOP (green) in LepR + SSCs, with or without MKs, after irradiation ( n = 6 per group). Scale bar, 100 µm. h Transmission electron microscopy images of LepR + SSCs after irradiation co-culture with MKs ( n = 3 per group). Data on graphs are shown as mean ± SD. One-way ANOVA was used to analyze the data in a – d and g . * P < 0.05, ** P < 0.01 and *** P < 0.001. For all panels in this figure, data are representative of three independent experiments.

Article Snippet: Briefly, the bone sections were incubated with primary antibodies against mouse osteocalcin (A20800, ABclonal), Ki67 (AF7617, R&D), PTP1B (bs-55182R, Bioss), Slc39a14 (A10413, ABclonal), leptin receptor (bs-0410R, Bioss), CHOP ( A21902 , ABclonal), F4/80 (30325, CST), TGFβ1 (ab313729, abcam), vWF (bsm-52775R, Bioss), osterix (ab209484, abcam) and Smad2 (A7699, ABclonal) overnight at 4 °C and incubated with secondary antibodies for 1 h at 37 °C.

Techniques: Concentration Assay, Irradiation, Immunostaining, Co-Culture Assay, Western Blot, Expressing, Transmission Assay, Electron Microscopy

a Representative immunostaining images of LepR (red) and PTP1B (green) in the BM of irradiated mice ( n = 6 mice per group). Scale bar, 100 µm. b Representative immunostaining images of LepR (red) and PTP1B (green) in the BM of MK deleted mice and their littermate controls after irradiation ( n = 6 mice per group). Scale bar, 100 µm. c Representative immunostaining images of PTP1B in LepR + cells, with or without, MKs from the BM of TGFβ1 MKΔ/Δ and TGFβ1 fl/fl mice after irradiation ( n = 6 per group). Scale bar, 100 µm. d Western blotting analysis of the expression of PTP1B and p-Stat3 in LepR + SSCs after co-culture with MKs ( n = 3 per group), inh = inhibitor. e Western blotting analysis of the expression of PTP1B and p-Stat3 in LepR + SSCs after co-culture with MKs from the BM of TGFβ1 MKΔ/Δ and TGFβ1 fl/fl mice ( n = 3 per group). Data on graphs are shown as mean ± SD. One-way ANOVA was used to analyze the data in c and d . * P < 0.05, ** P < 0.01 and *** P < 0.001. For all panels in this figure, data are representative of three independent experiments.

Journal: Experimental & Molecular Medicine

Article Title: Megakaryocytic TGFβ1 orchestrates osteogenesis of LepR + SSCs to alleviate radiation-induced bone loss

doi: 10.1038/s12276-025-01612-z

Figure Lengend Snippet: a Representative immunostaining images of LepR (red) and PTP1B (green) in the BM of irradiated mice ( n = 6 mice per group). Scale bar, 100 µm. b Representative immunostaining images of LepR (red) and PTP1B (green) in the BM of MK deleted mice and their littermate controls after irradiation ( n = 6 mice per group). Scale bar, 100 µm. c Representative immunostaining images of PTP1B in LepR + cells, with or without, MKs from the BM of TGFβ1 MKΔ/Δ and TGFβ1 fl/fl mice after irradiation ( n = 6 per group). Scale bar, 100 µm. d Western blotting analysis of the expression of PTP1B and p-Stat3 in LepR + SSCs after co-culture with MKs ( n = 3 per group), inh = inhibitor. e Western blotting analysis of the expression of PTP1B and p-Stat3 in LepR + SSCs after co-culture with MKs from the BM of TGFβ1 MKΔ/Δ and TGFβ1 fl/fl mice ( n = 3 per group). Data on graphs are shown as mean ± SD. One-way ANOVA was used to analyze the data in c and d . * P < 0.05, ** P < 0.01 and *** P < 0.001. For all panels in this figure, data are representative of three independent experiments.

Techniques: Immunostaining, Irradiation, Western Blot, Expressing, Co-Culture Assay

$a Representative micro-CT images of longitudinal section femurs, cross-sectional view of the distal femurs and reconstructed trabecular structure of the region of interest from Slc39a14 leprΔ/Δ mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 mice per group). b Quantitative micro-CT analysis of the TB fraction (BV/TV, Tb.N, Tb.Th, Tb.Sp, BMD and Ct.Th) in Slc39a14 leprΔ/Δ mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 mice per group). c Quantitative biomechanical analysis of femora (peak load and stiffness) from MK deleted mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 mice per group). d Serum zinc concentration in Slc39a14 leprΔ/Δ mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 per group). e Von Kossa staining showing mineralization of bone matrix in Slc39a14 leprΔ/Δ mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 per group). f Representative micro-CT images of longitudinal section femurs, cross-sectional view of the distal femurs and reconstructed trabecular structure of the region of interest from Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation ( n = 6 mice per group). g Representative immunostaining images of OCN (red) in the TB and EB of the Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation. The quantification of OCN cells is shown on the right ( n = 6 mice per group). Scale bar, 100 µm. h Representative immunostaining images of LepR (red) and PTP1B (green) in the BM of the Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation. Scale bar, 100 µm. i Colocalization of LepR (red) with Ki67 (green) in the BM of the Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation ( n = 6 mice per group). Scale bar, 100 µm. j Representative immunostaining images of TUNEL (green) in the BM of the Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation. The quantification of tunel positive cells is shown on the right ( n = 6 mice per group). Scale bar, 100 µm. Data on graphs are shown as mean ± SD. An unpaired two-tailed t -test was used to analyze the data in b – d , g , i and j . * P < 0.05, ** P < 0.01 and *** P < 0.001. For all panels in this figure, data are representative of three independent experiments.$

Journal: Experimental & Molecular Medicine

Article Title: Megakaryocytic TGFβ1 orchestrates osteogenesis of LepR + SSCs to alleviate radiation-induced bone loss

doi: 10.1038/s12276-025-01612-z

Figure Lengend Snippet: a Representative micro-CT images of longitudinal section femurs, cross-sectional view of the distal femurs and reconstructed trabecular structure of the region of interest from Slc39a14 leprΔ/Δ mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 mice per group). b Quantitative micro-CT analysis of the TB fraction (BV/TV, Tb.N, Tb.Th, Tb.Sp, BMD and Ct.Th) in Slc39a14 leprΔ/Δ mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 mice per group). c Quantitative biomechanical analysis of femora (peak load and stiffness) from MK deleted mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 mice per group). d Serum zinc concentration in Slc39a14 leprΔ/Δ mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 per group). e Von Kossa staining showing mineralization of bone matrix in Slc39a14 leprΔ/Δ mice and their littermate controls (Slc39a14 fl/fl mice) ( n = 6 per group). f Representative micro-CT images of longitudinal section femurs, cross-sectional view of the distal femurs and reconstructed trabecular structure of the region of interest from Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation ( n = 6 mice per group). g Representative immunostaining images of OCN (red) in the TB and EB of the Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation. The quantification of OCN cells is shown on the right ( n = 6 mice per group). Scale bar, 100 µm. h Representative immunostaining images of LepR (red) and PTP1B (green) in the BM of the Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation. Scale bar, 100 µm. i Colocalization of LepR (red) with Ki67 (green) in the BM of the Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation ( n = 6 mice per group). Scale bar, 100 µm. j Representative immunostaining images of TUNEL (green) in the BM of the Slc39a14 leprΔ/Δ mice injected with TPO or vehicle after irradiation. The quantification of tunel positive cells is shown on the right ( n = 6 mice per group). Scale bar, 100 µm. Data on graphs are shown as mean ± SD. An unpaired two-tailed t -test was used to analyze the data in b – d , g , i and j . * P < 0.05, ** P < 0.01 and *** P < 0.001. For all panels in this figure, data are representative of three independent experiments.

Techniques: Micro-CT, Concentration Assay, Staining, Injection, Irradiation, Immunostaining, TUNEL Assay, Two Tailed Test

Journal: Cell reports

Article Title: Context-dependent inhibitory roles of RhoA in 3D invasive cell migration within the extracellular matrix

doi: 10.1016/j.celrep.2025.116649

Figure Lengend Snippet: (A) Single WT and RHOA-KO HEK293 cells were seeded in Geltrex and monitored for 12 days in the presence of 30 μM PTP1B-IN-4. The culture medium containing PTP1B-IN-4 was replaced every 4 days. Scale bar, 50 μm. (B) Quantification of inverse circularity (mean ± SD, n = 3 experiments). (C) Wound-healing assay was performed in the presence of 30 μM PTP1B-IN-4 using WT and RHOA-KO HEK293 cells. Scale bar, 400 μm. (D) Quantification of wound closure (relative wound width over initial width, mean ± SD, n = 3 experiments). Statistical analysis: one-way ANOVA with post hoc Tukey (B and C): * p < 0.05.

Article Snippet: The inhibitor assay was performed using PTP1B-IN-4 (HY-15756, MedChemExpress), PTP1B-IN-2 (HY-100462), EHT 1864 (HY-16659), NSC 23766 trihydrochloride (HY-15723A), ML141 (HY-12755), and MLS-573151 (HY-113849).

Techniques: Wound Healing Assay

CHPT1 may regulate SLC7A11 transcription by phosphorylating STAT3. A. The results of protein profiling after immunoprecipitation performed by CHPT1 were intersected with the list of transcription factors predicted for SLC7A11 taken to find STAT3. B. Immunoprecipitation (Co-IP) assay to verify the direct interaction of CHPT1 with STAT3. C-D Representative images of immunofluorescence staining showing the colocalization of CHPT1 (red) and STAT3 (green) in PDAC cells. DAPI: blue, nucleus. Line chart of fluorescence signal positioning analysis. E. Protein expression levels of phosphorylated Y705 STAT3 after knockdown and overexpression of CHPT1. F. Protein expression levels of SLC7A11 after treatment with Stattic, an inhibitor of phosphorylated STAT3-Y705 to knockdown CHPT1 cells(5μM and 10μM). G. Co-IP assay confirmed the physical binding of PTPN1 to STAT3. H. CHPT1 overexpression promotes the binding of PTPN1 to STAT3. IP was performed under WB quantification and the differences were significant. I. Immunocytofluorescence analysis showed that overexpression of CHPT1 inhibited the nuclear translocation of pSTAT3.

Journal: Translational Oncology

Article Title: The CHPT-pSTAT3-SLC7A11 signaling axis controls progression and ferroptosis susceptibility of pancreatic cancer

doi: 10.1016/j.tranon.2025.102624

Figure Lengend Snippet: CHPT1 may regulate SLC7A11 transcription by phosphorylating STAT3. A. The results of protein profiling after immunoprecipitation performed by CHPT1 were intersected with the list of transcription factors predicted for SLC7A11 taken to find STAT3. B. Immunoprecipitation (Co-IP) assay to verify the direct interaction of CHPT1 with STAT3. C-D Representative images of immunofluorescence staining showing the colocalization of CHPT1 (red) and STAT3 (green) in PDAC cells. DAPI: blue, nucleus. Line chart of fluorescence signal positioning analysis. E. Protein expression levels of phosphorylated Y705 STAT3 after knockdown and overexpression of CHPT1. F. Protein expression levels of SLC7A11 after treatment with Stattic, an inhibitor of phosphorylated STAT3-Y705 to knockdown CHPT1 cells(5μM and 10μM). G. Co-IP assay confirmed the physical binding of PTPN1 to STAT3. H. CHPT1 overexpression promotes the binding of PTPN1 to STAT3. IP was performed under WB quantification and the differences were significant. I. Immunocytofluorescence analysis showed that overexpression of CHPT1 inhibited the nuclear translocation of pSTAT3.

Article Snippet: After clearing non-specific binding proteins with protein A/G-agarose beads (Selleck, USA), cell lysates were incubated with primary antibodies against CHPT1 (1:100, Santa), STAT3 (1:100, Proteintech), PTPN1(1:100, Proteintech), and IgG control (1:100, Proteintech) overnight at 4°C.

Techniques: Immunoprecipitation, Co-Immunoprecipitation Assay, Immunofluorescence, Staining, Fluorescence, Expressing, Knockdown, Over Expression, Binding Assay, Translocation Assay

PTPN1 is the critical effector of CHPT1 in suppressing STAT3-driven PDAC progression. A. Western blot analysis confirming efficient knockdown of PTPN1 in CHPT1-overexpressing PDAC cells. B-D. EDU incorporation assays showing that PTPN1 depletion restores cell proliferation despite CHPT1 overexpression. C. CCK-8 assays demonstrating that PTPN1 knockdown rescues the proliferative capacity of CHPT1-overexpressing cells. E. Transwell migration assays revealing the restoration of migratory potential upon PTPN1 silencing in CHPT1-overexpressing cells. F. Wound healing assays further confirming that PTPN1 depletion reverses the anti-migratory effects of CHPT1 overexpression. All data are presented as mean ± SD from 3 independent experiments (n=3).

Journal: Translational Oncology

Article Title: The CHPT-pSTAT3-SLC7A11 signaling axis controls progression and ferroptosis susceptibility of pancreatic cancer

doi: 10.1016/j.tranon.2025.102624

Figure Lengend Snippet: PTPN1 is the critical effector of CHPT1 in suppressing STAT3-driven PDAC progression. A. Western blot analysis confirming efficient knockdown of PTPN1 in CHPT1-overexpressing PDAC cells. B-D. EDU incorporation assays showing that PTPN1 depletion restores cell proliferation despite CHPT1 overexpression. C. CCK-8 assays demonstrating that PTPN1 knockdown rescues the proliferative capacity of CHPT1-overexpressing cells. E. Transwell migration assays revealing the restoration of migratory potential upon PTPN1 silencing in CHPT1-overexpressing cells. F. Wound healing assays further confirming that PTPN1 depletion reverses the anti-migratory effects of CHPT1 overexpression. All data are presented as mean ± SD from 3 independent experiments (n=3).

Techniques: Western Blot, Knockdown, Over Expression, CCK-8 Assay, Migration

PTP1B crystal cluster and inhibitor database analysis. A. The clustering results of collected PTP1B crystals (The PTP1B was divided into 10 clusters and the representative protein was shown in green); B. Chemical space analysis of the training set (yellow) and the test set (red) by principle component analysis.

Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

Article Title: Identification of novel PTP1B inhibitor for the treatment of LPS-induced myocardial apoptosis: machine learning based virtual screening and biological evaluation

doi: 10.1080/14756366.2025.2596950

Figure Lengend Snippet: PTP1B crystal cluster and inhibitor database analysis. A. The clustering results of collected PTP1B crystals (The PTP1B was divided into 10 clusters and the representative protein was shown in green); B. Chemical space analysis of the training set (yellow) and the test set (red) by principle component analysis.

Article Snippet: The primary antibody PTP1B (Rabbit, dilution: 1: 2000, RRID number: AB_10642566, Cat. NO.: 11334–1-AP) and TCPTP (Rabbit, dilution: 1: 500, RRID number: AB_2173235, Cat. NO.: 11214–1-AP) were purchased from Proteintech.

Techniques:

Pharmacophores produced by selected PTP1B crystal (Green: hydrogen bond acceptor; light blue: Hydrophobic group; dark blue: Hydrophobic group; yellow: Hydrogen bond donor; orange: Aromatic ring; gray: steric hindrance).

Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

Article Title: Identification of novel PTP1B inhibitor for the treatment of LPS-induced myocardial apoptosis: machine learning based virtual screening and biological evaluation

doi: 10.1080/14756366.2025.2596950

Figure Lengend Snippet: Pharmacophores produced by selected PTP1B crystal (Green: hydrogen bond acceptor; light blue: Hydrophobic group; dark blue: Hydrophobic group; yellow: Hydrogen bond donor; orange: Aromatic ring; gray: steric hindrance).

Techniques: Produced

The structures, activities and binding modes of selected compounds. A. The structures of selected compounds through virtual screening; B. PTP1B inhibitory rate of selected compounds at the concentration of 20 μM; C. The IC 50 value of PI-2 against PTP1B; D. The binding modes of PI-2 with PTP1B through molecular docking.

Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

Article Title: Identification of novel PTP1B inhibitor for the treatment of LPS-induced myocardial apoptosis: machine learning based virtual screening and biological evaluation

doi: 10.1080/14756366.2025.2596950

Figure Lengend Snippet: The structures, activities and binding modes of selected compounds. A. The structures of selected compounds through virtual screening; B. PTP1B inhibitory rate of selected compounds at the concentration of 20 μM; C. The IC 50 value of PI-2 against PTP1B; D. The binding modes of PI-2 with PTP1B through molecular docking.

Techniques: Binding Assay, Concentration Assay

The PTP1B inhibitory selectivity of PI-2 at the enzymatic and the cellular level. A. The IC 50 value of PI-2 against TCPTP; B. The IC 50 value of PI-2 against ACP1; C-E. The effect of PI-2 on the stability of PTP1B and TCPTP in AC16 cells.

Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

Article Title: Identification of novel PTP1B inhibitor for the treatment of LPS-induced myocardial apoptosis: machine learning based virtual screening and biological evaluation

doi: 10.1080/14756366.2025.2596950

Figure Lengend Snippet: The PTP1B inhibitory selectivity of PI-2 at the enzymatic and the cellular level. A. The IC 50 value of PI-2 against TCPTP; B. The IC 50 value of PI-2 against ACP1; C-E. The effect of PI-2 on the stability of PTP1B and TCPTP in AC16 cells.

Techniques:

The effect of PI-2 on mitochondrial membrane potential through PTP1B/JNK pathway. A. The effect of PI-2 on the phosphorylation level of JNK; B. The effect of PI-2 on mitochondrial membrane potential.

Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

Article Title: Identification of novel PTP1B inhibitor for the treatment of LPS-induced myocardial apoptosis: machine learning based virtual screening and biological evaluation

doi: 10.1080/14756366.2025.2596950

Figure Lengend Snippet: The effect of PI-2 on mitochondrial membrane potential through PTP1B/JNK pathway. A. The effect of PI-2 on the phosphorylation level of JNK; B. The effect of PI-2 on mitochondrial membrane potential.

Techniques: Membrane, Phospho-proteomics

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