goat anti-mouse antibody Search Results


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  • 99
    Vector Laboratories goat antimouse antibody
    Goat Antimouse Antibody, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse antibody/product/Vector Laboratories
    Average 99 stars, based on 14 article reviews
    Price from $9.99 to $1999.99
    goat antimouse antibody - by Bioz Stars, 2020-08
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    94
    Thermo Fisher goat antimouse secondary antibody
    Goat Antimouse Secondary Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 62 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse secondary antibody/product/Thermo Fisher
    Average 94 stars, based on 62 article reviews
    Price from $9.99 to $1999.99
    goat antimouse secondary antibody - by Bioz Stars, 2020-08
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    95
    Millipore goat antimouse antibody
    Goat Antimouse Antibody, supplied by Millipore, used in various techniques. Bioz Stars score: 95/100, based on 39 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse antibody/product/Millipore
    Average 95 stars, based on 39 article reviews
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    95
    Thermo Fisher goat antimouse igg antibody
    Goat Antimouse Igg Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse igg antibody/product/Thermo Fisher
    Average 95 stars, based on 5 article reviews
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    94
    Millipore goat mab antimouse igg1
    Inhibition of angiogenesis by APN inhibitors. A , mice developing hypoxia-induced retinal neovasculature were treated i.v. with PBS ( Vehicle ), <t>antimouse</t> APN antibodies or normal rat <t>IgG</t> (250 μ g/mouse), or bestatin (200 μ g/mouse). The number of retinal neovessels in mice treated with PBS was set at 100%. Data represent means; n = 3; bars, SE. The reduction in blood vessel number was statistically significant for the anti-APN antibodies and bestatin ( P
    Goat Mab Antimouse Igg1, supplied by Millipore, used in various techniques. Bioz Stars score: 94/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat mab antimouse igg1/product/Millipore
    Average 94 stars, based on 20 article reviews
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    96
    Bethyl antibodies goat antimouse albumin
    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat <t>antimouse</t> Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.
    Antibodies Goat Antimouse Albumin, supplied by Bethyl, used in various techniques. Bioz Stars score: 96/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/antibodies goat antimouse albumin/product/Bethyl
    Average 96 stars, based on 10 article reviews
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    94
    Millipore goat antimouse polyvalent antibody
    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat <t>antimouse</t> Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.
    Goat Antimouse Polyvalent Antibody, supplied by Millipore, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse polyvalent antibody/product/Millipore
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    99
    Bio-Rad goat antimouse igg antibodies
    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat <t>antimouse</t> Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.
    Goat Antimouse Igg Antibodies, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse igg antibodies/product/Bio-Rad
    Average 99 stars, based on 13 article reviews
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    goat antimouse igg antibodies - by Bioz Stars, 2020-08
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    97
    Thermo Fisher goat antimouse
    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat <t>antimouse</t> Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.
    Goat Antimouse, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 363 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse/product/Thermo Fisher
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    94
    Bio-Rad goat antimouse antibody
    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat <t>antimouse</t> Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.
    Goat Antimouse Antibody, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse antibody/product/Bio-Rad
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    goat antimouse antibody - by Bioz Stars, 2020-08
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    99
    Jackson Immuno goat antimouse antibody
    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat <t>antimouse</t> Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.
    Goat Antimouse Antibody, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 99/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse antibody/product/Jackson Immuno
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    goat antimouse antibody - by Bioz Stars, 2020-08
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    99
    Vector Laboratories biotinylated goat antimouse antibody
    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat <t>antimouse</t> Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.
    Biotinylated Goat Antimouse Antibody, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    95
    Abcam goat antimouse antibody
    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat <t>antimouse</t> Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.
    Goat Antimouse Antibody, supplied by Abcam, used in various techniques. Bioz Stars score: 95/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat antimouse antibody/product/Abcam
    Average 95 stars, based on 4 article reviews
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    goat antimouse antibody - by Bioz Stars, 2020-08
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    Image Search Results


    Inhibition of angiogenesis by APN inhibitors. A , mice developing hypoxia-induced retinal neovasculature were treated i.v. with PBS ( Vehicle ), antimouse APN antibodies or normal rat IgG (250 μ g/mouse), or bestatin (200 μ g/mouse). The number of retinal neovessels in mice treated with PBS was set at 100%. Data represent means; n = 3; bars, SE. The reduction in blood vessel number was statistically significant for the anti-APN antibodies and bestatin ( P

    Journal: Cancer research

    Article Title: Aminopeptidase N Is a Receptor for Tumor-homing Peptides and a Target for Inhibiting Angiogenesis

    doi:

    Figure Lengend Snippet: Inhibition of angiogenesis by APN inhibitors. A , mice developing hypoxia-induced retinal neovasculature were treated i.v. with PBS ( Vehicle ), antimouse APN antibodies or normal rat IgG (250 μ g/mouse), or bestatin (200 μ g/mouse). The number of retinal neovessels in mice treated with PBS was set at 100%. Data represent means; n = 3; bars, SE. The reduction in blood vessel number was statistically significant for the anti-APN antibodies and bestatin ( P

    Article Snippet: Alternatively, fluorescently labeled antimouse IgG (Sigma) was used for detecting the primary antibody.

    Techniques: Inhibition, Mouse Assay

    Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat antimouse Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: The peripheral chimerism of bone marrow–derived stem cells after transplantation: regeneration of gastrointestinal tissues in lethally irradiated mice

    doi: 10.1111/jcmm.12227

    Figure Lengend Snippet: Isolation of lin − Sca-1 + cells by FACS. The cell sorting was carried out on a FACS ARIA II cell sorter (Becton Dickinson). Before sorting, a bone marrow cell suspension (5 × 10 6 /ml) isolated from green fluorescent protein (GFP) mice was sorted for the presence of the GFP protein or incubated with 40 μl of biotin mouse Lineage Depletion Cocktail (BD IMAg™) and 5 μl rat antimouse Ly-6A/E(Sca-1)-APC (clone D7; Southern Biotech) for 30 min. at 4°C. Then, the cells were washed twice in Iscove*s modified Dulbecco*s Medium (IMDM) and stained with 5 μl of PE Streptavidin (BD Pharmingen; 15 min., 4°C). The cells were then washed twice in IMDM medium. The sorting gates were set (Fig. 1 A–C), and sorted GFP + lin − Sca-1 + cells were collected in a tube containing IMDM medium with 2% FCS. ( A ) before sorting bone marrow cells by size (SSC) and granularity (FSC); ( B ) cell sorting and selection of GFP + cells (quadrant R2); ( C ) the selected cells GFP + lin − (lin-Str-PE) Sca-1 + (Sca-APC) for applications; selected cells represent about 0.7% of GFP + cells in the bone marrow. After sorting, an aliquot of the sorted cells was run on the FACS ARIA II to check the purity of the cell population (Fig. 1 D–F); ( D ) cell profile after sorting; virtually all cells are small with minimal granularity; ( E ) all cells are GFP + ; and ( F ) the final product is 96% sorted GFP + lin − Sca-1 + cells.

    Article Snippet: For detection of antigens, briefly, the tissue sections were incubated with the primary antibodies goat antimouse albumin (Bethyl Laboratories Inc., Montgomery, TX, USA) and rat antimouse CD31 (BioLegend, San Diego, CA, USA) for 1 hr.

    Techniques: Isolation, FACS, Mouse Assay, Incubation, Modification, Staining, Selection