human her2 protein Search Results


95
Sino Biological fc her2 receptor
Fc Her2 Receptor, supplied by Sino Biological, 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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R&D Systems human erbb2 her2 fc chimera
Human Erbb2 Her2 Fc Chimera, supplied by R&D Systems, 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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95
Sino Biological biotinylated hher2
Biotinylated Hher2, supplied by Sino Biological, 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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95
Sino Biological her2 erbb2 ecd
Her2 Erbb2 Ecd, supplied by Sino Biological, 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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95
Sino Biological h08h

H08h, supplied by Sino Biological, 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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h08h - by Bioz Stars, 2026-03
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93
OriGene her2
(A) Schematic of AT1R-EGFR BRET-based transactivation. EGFR fused to a BRET donor (Rluc8), is co-transfected with Grb2 adaptor protein tagged with a BRET acceptor (Venus) and the AT1R. Stimulation of the AT1R promotes activation of the EGFR and recruitment of Grb2. (B) HEK293 cells expressing AT1R, EGFR-Rluc8, and Grb2-Venus were treated with 10μM AngII, 1μM EGF or vehicle. Quantification of ligand-induced BRET ratio (maximum-minimum) between EGFR-Rluc8 and Grb2-Venus following AngII- and EGF-stimulation. Insert is HEK293 cells (stably expressing AT1R) stimulated with 100nM AngII, 10nM EGF or vehicle for 5 minutes before processing for phospho-ERK1/2:total-ERK1/2 (p-ERK:T-ERK) western blots. Blots are representative of 3 independent experiments (B inset) Cells expressing AT1R, Grb2-Venus and either EGFR-Rluc8, <t>HER2-Rluc8</t> or HER3-Rluc8 and stimulated with 10μM AngII. Agonist stimulation is indicated by arrow. Data represent mean ± SEM of 3 independent experiments.
Her2, supplied by OriGene, 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/her2/product/OriGene
Average 93 stars, based on 1 article reviews
her2 - by Bioz Stars, 2026-03
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95
R&D Systems her2 protein
(A) Schematic of AT1R-EGFR BRET-based transactivation. EGFR fused to a BRET donor (Rluc8), is co-transfected with Grb2 adaptor protein tagged with a BRET acceptor (Venus) and the AT1R. Stimulation of the AT1R promotes activation of the EGFR and recruitment of Grb2. (B) HEK293 cells expressing AT1R, EGFR-Rluc8, and Grb2-Venus were treated with 10μM AngII, 1μM EGF or vehicle. Quantification of ligand-induced BRET ratio (maximum-minimum) between EGFR-Rluc8 and Grb2-Venus following AngII- and EGF-stimulation. Insert is HEK293 cells (stably expressing AT1R) stimulated with 100nM AngII, 10nM EGF or vehicle for 5 minutes before processing for phospho-ERK1/2:total-ERK1/2 (p-ERK:T-ERK) western blots. Blots are representative of 3 independent experiments (B inset) Cells expressing AT1R, Grb2-Venus and either EGFR-Rluc8, <t>HER2-Rluc8</t> or HER3-Rluc8 and stimulated with 10μM AngII. Agonist stimulation is indicated by arrow. Data represent mean ± SEM of 3 independent experiments.
Her2 Protein, supplied by R&D Systems, 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/her2 protein/product/R&D Systems
Average 95 stars, based on 1 article reviews
her2 protein - by Bioz Stars, 2026-03
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93
R&D Systems human her2
(A) Schematic of AT1R-EGFR BRET-based transactivation. EGFR fused to a BRET donor (Rluc8), is co-transfected with Grb2 adaptor protein tagged with a BRET acceptor (Venus) and the AT1R. Stimulation of the AT1R promotes activation of the EGFR and recruitment of Grb2. (B) HEK293 cells expressing AT1R, EGFR-Rluc8, and Grb2-Venus were treated with 10μM AngII, 1μM EGF or vehicle. Quantification of ligand-induced BRET ratio (maximum-minimum) between EGFR-Rluc8 and Grb2-Venus following AngII- and EGF-stimulation. Insert is HEK293 cells (stably expressing AT1R) stimulated with 100nM AngII, 10nM EGF or vehicle for 5 minutes before processing for phospho-ERK1/2:total-ERK1/2 (p-ERK:T-ERK) western blots. Blots are representative of 3 independent experiments (B inset) Cells expressing AT1R, Grb2-Venus and either EGFR-Rluc8, <t>HER2-Rluc8</t> or HER3-Rluc8 and stimulated with 10μM AngII. Agonist stimulation is indicated by arrow. Data represent mean ± SEM of 3 independent experiments.
Human Her2, supplied by R&D Systems, 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/human her2/product/R&D Systems
Average 93 stars, based on 1 article reviews
human her2 - by Bioz Stars, 2026-03
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95
Sino Biological human her2 10004 hcch extracellular domain
Molecular and hydrodynamic properties of the mAbs and target <t> HER2; </t> molecular weight (M w ), intrinsic viscosity ([η]), hydrodynamic radius (r h ), and UV coefficient of absorption at 280 nm (dA/dc).
Human Her2 10004 Hcch Extracellular Domain, supplied by Sino Biological, 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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human her2 10004 hcch extracellular domain - by Bioz Stars, 2026-03
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94
R&D Systems recombinant histidine tagged human her2 proteins
Molecular and hydrodynamic properties of the mAbs and target <t> HER2; </t> molecular weight (M w ), intrinsic viscosity ([η]), hydrodynamic radius (r h ), and UV coefficient of absorption at 280 nm (dA/dc).
Recombinant Histidine Tagged Human Her2 Proteins, supplied by R&D Systems, 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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93
Boster Bio c erbb 2
Molecular and hydrodynamic properties of the mAbs and target <t> HER2; </t> molecular weight (M w ), intrinsic viscosity ([η]), hydrodynamic radius (r h ), and UV coefficient of absorption at 280 nm (dA/dc).
C Erbb 2, supplied by Boster Bio, 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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93
MedChemExpress human mce cat
Molecular and hydrodynamic properties of the mAbs and target <t> HER2; </t> molecular weight (M w ), intrinsic viscosity ([η]), hydrodynamic radius (r h ), and UV coefficient of absorption at 280 nm (dA/dc).
Human Mce Cat, 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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Image Search Results


Journal: Cell Reports Methods

Article Title: Sequence enrichment profiles enable target-agnostic antibody generation for a broad range of antigens

doi: 10.1016/j.crmeth.2023.100475

Figure Lengend Snippet:

Article Snippet: HER2 , Sino Biological , Cat# 10004-H08H.

Techniques: Produced, Recombinant, Sequencing, Software

(A) Schematic of AT1R-EGFR BRET-based transactivation. EGFR fused to a BRET donor (Rluc8), is co-transfected with Grb2 adaptor protein tagged with a BRET acceptor (Venus) and the AT1R. Stimulation of the AT1R promotes activation of the EGFR and recruitment of Grb2. (B) HEK293 cells expressing AT1R, EGFR-Rluc8, and Grb2-Venus were treated with 10μM AngII, 1μM EGF or vehicle. Quantification of ligand-induced BRET ratio (maximum-minimum) between EGFR-Rluc8 and Grb2-Venus following AngII- and EGF-stimulation. Insert is HEK293 cells (stably expressing AT1R) stimulated with 100nM AngII, 10nM EGF or vehicle for 5 minutes before processing for phospho-ERK1/2:total-ERK1/2 (p-ERK:T-ERK) western blots. Blots are representative of 3 independent experiments (B inset) Cells expressing AT1R, Grb2-Venus and either EGFR-Rluc8, HER2-Rluc8 or HER3-Rluc8 and stimulated with 10μM AngII. Agonist stimulation is indicated by arrow. Data represent mean ± SEM of 3 independent experiments.

Journal: Biochemical pharmacology

Article Title: BRET-based assay to monitor EGFR transactivation by the AT 1 R reveals G q/11 protein-independent activation and AT 1 R-EGFR complexes

doi: 10.1016/j.bcp.2018.10.017

Figure Lengend Snippet: (A) Schematic of AT1R-EGFR BRET-based transactivation. EGFR fused to a BRET donor (Rluc8), is co-transfected with Grb2 adaptor protein tagged with a BRET acceptor (Venus) and the AT1R. Stimulation of the AT1R promotes activation of the EGFR and recruitment of Grb2. (B) HEK293 cells expressing AT1R, EGFR-Rluc8, and Grb2-Venus were treated with 10μM AngII, 1μM EGF or vehicle. Quantification of ligand-induced BRET ratio (maximum-minimum) between EGFR-Rluc8 and Grb2-Venus following AngII- and EGF-stimulation. Insert is HEK293 cells (stably expressing AT1R) stimulated with 100nM AngII, 10nM EGF or vehicle for 5 minutes before processing for phospho-ERK1/2:total-ERK1/2 (p-ERK:T-ERK) western blots. Blots are representative of 3 independent experiments (B inset) Cells expressing AT1R, Grb2-Venus and either EGFR-Rluc8, HER2-Rluc8 or HER3-Rluc8 and stimulated with 10μM AngII. Agonist stimulation is indicated by arrow. Data represent mean ± SEM of 3 independent experiments.

Article Snippet: EGFR-Rluc8, HER2-Rluc8 and HER3-Rluc8 were generated by inserting EGFR, HER2, and HER3, obtained from Origene (Rockville, MD, USA) into pcDNA3-Rluc8.

Techniques: Transfection, Activation Assay, Expressing, Stable Transfection, Western Blot

Molecular and hydrodynamic properties of the mAbs and target  HER2;  molecular weight (M w ), intrinsic viscosity ([η]), hydrodynamic radius (r h ), and UV coefficient of absorption at 280 nm (dA/dc).

Journal: International Journal of Molecular Sciences

Article Title: Exploring the Combined Action of Adding Pertuzumab to Branded Trastuzumab versus Trastuzumab Biosimilars for Treating HER2+ Breast Cancer

doi: 10.3390/ijms25073940

Figure Lengend Snippet: Molecular and hydrodynamic properties of the mAbs and target HER2; molecular weight (M w ), intrinsic viscosity ([η]), hydrodynamic radius (r h ), and UV coefficient of absorption at 280 nm (dA/dc).

Article Snippet: The human HER2 (10004-HCCH) extracellular domain was purchased from Sino Biological, Inc.

Techniques: Molecular Weight, Viscosity

Molecular and hydrodynamic properties of the complexes (case 1); molecular weight, intrinsic viscosity, hydrodynamic radius, and UV coefficient of absorption at 280 nm.

Journal: International Journal of Molecular Sciences

Article Title: Exploring the Combined Action of Adding Pertuzumab to Branded Trastuzumab versus Trastuzumab Biosimilars for Treating HER2+ Breast Cancer

doi: 10.3390/ijms25073940

Figure Lengend Snippet: Molecular and hydrodynamic properties of the complexes (case 1); molecular weight, intrinsic viscosity, hydrodynamic radius, and UV coefficient of absorption at 280 nm.

Article Snippet: The human HER2 (10004-HCCH) extracellular domain was purchased from Sino Biological, Inc.

Techniques: Molecular Weight, Viscosity

Molecular and hydrodynamic properties of the complexes (case 2); molecular weight, intrinsic viscosity, hydrodynamic radius, and UV coefficient of absorption at 280 nm.

Journal: International Journal of Molecular Sciences

Article Title: Exploring the Combined Action of Adding Pertuzumab to Branded Trastuzumab versus Trastuzumab Biosimilars for Treating HER2+ Breast Cancer

doi: 10.3390/ijms25073940

Figure Lengend Snippet: Molecular and hydrodynamic properties of the complexes (case 2); molecular weight, intrinsic viscosity, hydrodynamic radius, and UV coefficient of absorption at 280 nm.

Article Snippet: The human HER2 (10004-HCCH) extracellular domain was purchased from Sino Biological, Inc.

Techniques: Molecular Weight, Viscosity

Molecular and hydrodynamic properties of the complexes (case 3); molecular weight, intrinsic viscosity, hydrodynamic radius, and UV coefficient of absorption at 280 nm.

Journal: International Journal of Molecular Sciences

Article Title: Exploring the Combined Action of Adding Pertuzumab to Branded Trastuzumab versus Trastuzumab Biosimilars for Treating HER2+ Breast Cancer

doi: 10.3390/ijms25073940

Figure Lengend Snippet: Molecular and hydrodynamic properties of the complexes (case 3); molecular weight, intrinsic viscosity, hydrodynamic radius, and UV coefficient of absorption at 280 nm.

Article Snippet: The human HER2 (10004-HCCH) extracellular domain was purchased from Sino Biological, Inc.

Techniques: Molecular Weight, Viscosity

SEC traces of mAb/HER2 complexes in binary interaction. SEC traces (RI signal) of complexes between each trastuzumab biosimilar and HER2 ( left ), and comparison of trastuzumab/HER2 and pertuzumab/HER2 traces obtained in the same conditions ( right ).

Journal: International Journal of Molecular Sciences

Article Title: Exploring the Combined Action of Adding Pertuzumab to Branded Trastuzumab versus Trastuzumab Biosimilars for Treating HER2+ Breast Cancer

doi: 10.3390/ijms25073940

Figure Lengend Snippet: SEC traces of mAb/HER2 complexes in binary interaction. SEC traces (RI signal) of complexes between each trastuzumab biosimilar and HER2 ( left ), and comparison of trastuzumab/HER2 and pertuzumab/HER2 traces obtained in the same conditions ( right ).

Article Snippet: The human HER2 (10004-HCCH) extracellular domain was purchased from Sino Biological, Inc.

Techniques: Comparison

Schematic representation of the different complexes: HER2 extracellular domains (blue), trastuzumab (T, black) and pertuzumab (P, grey). The different HER2 domains are indicated in ( A ). ( A , D ) represents the complex 1 formed by trastuzumab and pertuzumab with HER2, respectively; ( B , E ) represent the complex 2 for tratuzumab and pertuzumab with HER2, respectively; and ( C , F ) represent the Complex 3, in which both mAbs are involved.

Journal: International Journal of Molecular Sciences

Article Title: Exploring the Combined Action of Adding Pertuzumab to Branded Trastuzumab versus Trastuzumab Biosimilars for Treating HER2+ Breast Cancer

doi: 10.3390/ijms25073940

Figure Lengend Snippet: Schematic representation of the different complexes: HER2 extracellular domains (blue), trastuzumab (T, black) and pertuzumab (P, grey). The different HER2 domains are indicated in ( A ). ( A , D ) represents the complex 1 formed by trastuzumab and pertuzumab with HER2, respectively; ( B , E ) represent the complex 2 for tratuzumab and pertuzumab with HER2, respectively; and ( C , F ) represent the Complex 3, in which both mAbs are involved.

Article Snippet: The human HER2 (10004-HCCH) extracellular domain was purchased from Sino Biological, Inc.

Techniques:

Comparison of the SEC traces obtained for the complexes in case 2 for ternary interaction. Upper panel: complete SEC-IR traces of the complexes and free mAb for case 2: black (HRC/HER2/PJT), red (ONT/HER2/PJT), and blue (HZM/HER2/PJT). Curves have been vertically shifted for better visualization. Bottom panel: measured absolute molecular weight obtained for the complexes.

Journal: International Journal of Molecular Sciences

Article Title: Exploring the Combined Action of Adding Pertuzumab to Branded Trastuzumab versus Trastuzumab Biosimilars for Treating HER2+ Breast Cancer

doi: 10.3390/ijms25073940

Figure Lengend Snippet: Comparison of the SEC traces obtained for the complexes in case 2 for ternary interaction. Upper panel: complete SEC-IR traces of the complexes and free mAb for case 2: black (HRC/HER2/PJT), red (ONT/HER2/PJT), and blue (HZM/HER2/PJT). Curves have been vertically shifted for better visualization. Bottom panel: measured absolute molecular weight obtained for the complexes.

Article Snippet: The human HER2 (10004-HCCH) extracellular domain was purchased from Sino Biological, Inc.

Techniques: Comparison, Molecular Weight

High-order complexes (M w ~930 kDa) between the mAbs trastuzumab, pertuzumab, and HER2. Pertuzumab again favors C2 complex in trastuzumab/HER2 interaction acting as linkers. HER2 extracellular domains (blue), trastuzumab (T, black), and pertuzumab (P, grey). The different domains of HER2 protein are indicated in different colors as in .

Journal: International Journal of Molecular Sciences

Article Title: Exploring the Combined Action of Adding Pertuzumab to Branded Trastuzumab versus Trastuzumab Biosimilars for Treating HER2+ Breast Cancer

doi: 10.3390/ijms25073940

Figure Lengend Snippet: High-order complexes (M w ~930 kDa) between the mAbs trastuzumab, pertuzumab, and HER2. Pertuzumab again favors C2 complex in trastuzumab/HER2 interaction acting as linkers. HER2 extracellular domains (blue), trastuzumab (T, black), and pertuzumab (P, grey). The different domains of HER2 protein are indicated in different colors as in .

Article Snippet: The human HER2 (10004-HCCH) extracellular domain was purchased from Sino Biological, Inc.

Techniques: