goat anti human cd220 apc Search Results


92
Bio-Techne corporation human/mouse insulin r/cd220 apc-conjugated antibody
Human/Mouse Insulin R/Cd220 Apc Conjugated Antibody, supplied by Bio-Techne corporation, 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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90
R&D Systems cd220
Cd220, supplied by R&D Systems, 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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90
Becton Dickinson mouse anti-insr (cd220
Mouse Anti Insr (Cd220, supplied by Becton Dickinson, 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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90
Bio-Rad rabbit anti human cd200
Figure 2. Confirmation of altered gene expression in lymphatics of T241/VEGF-C fibrosarcomas by comparative immunostaining. A, representative frozen sections of normal dermis and primary tumors from mice transplanted with either T-241 control or T-241/VEGF-C fibrosarcomas were dual immunostained for LYVE-1 (Alexa 488; green) and ESAM, Endoglin, or <t>CD200</t> (Alexa 568; red) to confirm the up-regulated gene expression seen in Affymetrix microarray analyses of isolated LEC (Fig. 1C). ESAM, Endoglin, and CD200 expression is restricted to LYVE-1–negative blood capillaries in normal skin and nonmetastatic control T-241 tumors but selectively up-regulated in intratumoral/peritumoral LYVE-1–positive lymphatic capillaries in metastatic T-241/VEGF-C fibrosarcomas (original magnification, 20). B, dual immunostaining for LYVE-1 and biglycan shows that the proteoglycan is abundant in the subendothelial matrix of LYVE-1–negative blood vessels and small LYVE-1–positive lymphatic capillaries in normal dermis and control nonmetastatic T-241 tumors but is absent from LYVE-1–positive lymphatics in metastatic T241/ VEGF-C fibrosarcomas (original magnification, 20). Arrowheads in selected images are included as points of reference for appropriate single or dual stained lymphatic capillaries.
Rabbit Anti Human Cd200, supplied by Bio-Rad, 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
rabbit anti human cd200 - by Bioz Stars, 2026-09
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96
Jackson Immuno rpe conjugated goat anti mouse igg
Figure 2. Confirmation of altered gene expression in lymphatics of T241/VEGF-C fibrosarcomas by comparative immunostaining. A, representative frozen sections of normal dermis and primary tumors from mice transplanted with either T-241 control or T-241/VEGF-C fibrosarcomas were dual immunostained for LYVE-1 (Alexa 488; green) and ESAM, Endoglin, or <t>CD200</t> (Alexa 568; red) to confirm the up-regulated gene expression seen in Affymetrix microarray analyses of isolated LEC (Fig. 1C). ESAM, Endoglin, and CD200 expression is restricted to LYVE-1–negative blood capillaries in normal skin and nonmetastatic control T-241 tumors but selectively up-regulated in intratumoral/peritumoral LYVE-1–positive lymphatic capillaries in metastatic T-241/VEGF-C fibrosarcomas (original magnification, 20). B, dual immunostaining for LYVE-1 and biglycan shows that the proteoglycan is abundant in the subendothelial matrix of LYVE-1–negative blood vessels and small LYVE-1–positive lymphatic capillaries in normal dermis and control nonmetastatic T-241 tumors but is absent from LYVE-1–positive lymphatics in metastatic T241/ VEGF-C fibrosarcomas (original magnification, 20). Arrowheads in selected images are included as points of reference for appropriate single or dual stained lymphatic capillaries.
Rpe Conjugated Goat Anti Mouse Igg, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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90
Boster Bio rabbit anti ir a
Figure 2. Confirmation of altered gene expression in lymphatics of T241/VEGF-C fibrosarcomas by comparative immunostaining. A, representative frozen sections of normal dermis and primary tumors from mice transplanted with either T-241 control or T-241/VEGF-C fibrosarcomas were dual immunostained for LYVE-1 (Alexa 488; green) and ESAM, Endoglin, or <t>CD200</t> (Alexa 568; red) to confirm the up-regulated gene expression seen in Affymetrix microarray analyses of isolated LEC (Fig. 1C). ESAM, Endoglin, and CD200 expression is restricted to LYVE-1–negative blood capillaries in normal skin and nonmetastatic control T-241 tumors but selectively up-regulated in intratumoral/peritumoral LYVE-1–positive lymphatic capillaries in metastatic T-241/VEGF-C fibrosarcomas (original magnification, 20). B, dual immunostaining for LYVE-1 and biglycan shows that the proteoglycan is abundant in the subendothelial matrix of LYVE-1–negative blood vessels and small LYVE-1–positive lymphatic capillaries in normal dermis and control nonmetastatic T-241 tumors but is absent from LYVE-1–positive lymphatics in metastatic T241/ VEGF-C fibrosarcomas (original magnification, 20). Arrowheads in selected images are included as points of reference for appropriate single or dual stained lymphatic capillaries.
Rabbit Anti Ir A, supplied by Boster Bio, 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/product/goat+anti+human+cd220+apc/Anti-Phospho-Insulin+Receptor+(Thr1160)+INSR+Antibody/pm26077651-81-13-28
Average 90 stars, based on 1 article reviews
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93
Proteintech blotting
Figure 2. Confirmation of altered gene expression in lymphatics of T241/VEGF-C fibrosarcomas by comparative immunostaining. A, representative frozen sections of normal dermis and primary tumors from mice transplanted with either T-241 control or T-241/VEGF-C fibrosarcomas were dual immunostained for LYVE-1 (Alexa 488; green) and ESAM, Endoglin, or <t>CD200</t> (Alexa 568; red) to confirm the up-regulated gene expression seen in Affymetrix microarray analyses of isolated LEC (Fig. 1C). ESAM, Endoglin, and CD200 expression is restricted to LYVE-1–negative blood capillaries in normal skin and nonmetastatic control T-241 tumors but selectively up-regulated in intratumoral/peritumoral LYVE-1–positive lymphatic capillaries in metastatic T-241/VEGF-C fibrosarcomas (original magnification, 20). B, dual immunostaining for LYVE-1 and biglycan shows that the proteoglycan is abundant in the subendothelial matrix of LYVE-1–negative blood vessels and small LYVE-1–positive lymphatic capillaries in normal dermis and control nonmetastatic T-241 tumors but is absent from LYVE-1–positive lymphatics in metastatic T241/ VEGF-C fibrosarcomas (original magnification, 20). Arrowheads in selected images are included as points of reference for appropriate single or dual stained lymphatic capillaries.
Blotting, supplied by Proteintech, 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
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Image Search Results


Figure 2. Confirmation of altered gene expression in lymphatics of T241/VEGF-C fibrosarcomas by comparative immunostaining. A, representative frozen sections of normal dermis and primary tumors from mice transplanted with either T-241 control or T-241/VEGF-C fibrosarcomas were dual immunostained for LYVE-1 (Alexa 488; green) and ESAM, Endoglin, or CD200 (Alexa 568; red) to confirm the up-regulated gene expression seen in Affymetrix microarray analyses of isolated LEC (Fig. 1C). ESAM, Endoglin, and CD200 expression is restricted to LYVE-1–negative blood capillaries in normal skin and nonmetastatic control T-241 tumors but selectively up-regulated in intratumoral/peritumoral LYVE-1–positive lymphatic capillaries in metastatic T-241/VEGF-C fibrosarcomas (original magnification, 20). B, dual immunostaining for LYVE-1 and biglycan shows that the proteoglycan is abundant in the subendothelial matrix of LYVE-1–negative blood vessels and small LYVE-1–positive lymphatic capillaries in normal dermis and control nonmetastatic T-241 tumors but is absent from LYVE-1–positive lymphatics in metastatic T241/ VEGF-C fibrosarcomas (original magnification, 20). Arrowheads in selected images are included as points of reference for appropriate single or dual stained lymphatic capillaries.

Journal: Cancer Research

Article Title: A Novel Gene Expression Profile in Lymphatics Associated with Tumor Growth and Nodal Metastasis

doi: 10.1158/0008-5472.can-07-6506

Figure Lengend Snippet: Figure 2. Confirmation of altered gene expression in lymphatics of T241/VEGF-C fibrosarcomas by comparative immunostaining. A, representative frozen sections of normal dermis and primary tumors from mice transplanted with either T-241 control or T-241/VEGF-C fibrosarcomas were dual immunostained for LYVE-1 (Alexa 488; green) and ESAM, Endoglin, or CD200 (Alexa 568; red) to confirm the up-regulated gene expression seen in Affymetrix microarray analyses of isolated LEC (Fig. 1C). ESAM, Endoglin, and CD200 expression is restricted to LYVE-1–negative blood capillaries in normal skin and nonmetastatic control T-241 tumors but selectively up-regulated in intratumoral/peritumoral LYVE-1–positive lymphatic capillaries in metastatic T-241/VEGF-C fibrosarcomas (original magnification, 20). B, dual immunostaining for LYVE-1 and biglycan shows that the proteoglycan is abundant in the subendothelial matrix of LYVE-1–negative blood vessels and small LYVE-1–positive lymphatic capillaries in normal dermis and control nonmetastatic T-241 tumors but is absent from LYVE-1–positive lymphatics in metastatic T241/ VEGF-C fibrosarcomas (original magnification, 20). Arrowheads in selected images are included as points of reference for appropriate single or dual stained lymphatic capillaries.

Article Snippet: Polyclonal goat anti-human ESAM, goat antihuman LYVE-1, and goat anti-mouse VEGF receptor 3 (VEGFR3) antibodies were from R&D Systems Europe; mouse anti-human Endoglin was from DAKO; polyclonal rabbit anti-human leptin-R antibodies were from Abcam; rat anti-mouse CD31, Endoglin, and MECA-32 monoclonal antibodies were from BD Pharmingen; rabbit anti-Prox1 was from Research Diagnostics Inc.; goat anti-mouse biglycan was from Santa Cruz Biotechnology; and rabbit anti-human CD200 was from Serotec UK.

Techniques: Gene Expression, Immunostaining, Control, Microarray, Isolation, Expressing, Staining