pig spleen tissue were subjected to SDS PAGE followed by western blot with 60287-1-Ig (CD45 Antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.

Immunohistochemical analysis of paraffin-embedded human appendicitis tissue slide using 60287-1-Ig (CD45 antibody) at dilution of 1:8000 (under 0x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

Immunohistochemical analysis of paraffin-embedded human appendicitis tissue slide using 60287-1-Ig (CD45 antibody) at dilution of 1:8000 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

Immunofluorescent analysis of (4% PFA) fixed mouse colon tissue using CD45 antibody (60287-1-Ig, Clone: 4E9B2 ) at dilution of 1:1000 and CoraLite®488-Conjugated AffiniPure Goat Anti-Mouse IgG(H+L).

Immunofluorescent analysis of (4% PFA) fixed mouse colon tissue using CD45 antibody (60287-1-Ig, Clone: 4E9B2 ) at dilution of 1:1000 and CoraLite®488-Conjugated AffiniPure Goat Anti-Mouse IgG(H+L).

pig spleen tissue were subjected to SDS PAGE followed by western blot with 60287-1-Ig (CD45 Antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 60287-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human appendicitis tissue slide using 60287-1-Ig (CD45 antibody) at dilution of 1:8000 (under 0x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 60287-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human appendicitis tissue slide using 60287-1-Ig (CD45 antibody) at dilution of 1:8000 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 60287-1-PBS in a different storage buffer formulation.

Immunofluorescent analysis of (4% PFA) fixed mouse colon tissue using CD45 antibody (60287-1-Ig, Clone: 4E9B2 ) at dilution of 1:1000 and CoraLite®488-Conjugated AffiniPure Goat Anti-Mouse IgG(H+L). This data was developed using the same antibody clone with 60287-1-PBS in a different storage buffer formulation.

Immunofluorescent analysis of (4% PFA) fixed mouse colon tissue using CD45 antibody (60287-1-Ig, Clone: 4E9B2 ) at dilution of 1:1000 and CoraLite®488-Conjugated AffiniPure Goat Anti-Mouse IgG(H+L). This data was developed using the same antibody clone with 60287-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human tonsillitis tissue slide using KHC0031 (CD45 IHC Kit).

Immunohistochemical analysis of paraffin-embedded human appendicitis tissue slide using KHC0031 (CD45 IHC Kit).

Immunohistochemical analysis of paraffin-embedded human liver tissue slide using KHC0031 (CD45 IHC Kit).

G65109-1-5C was used to stain Resting PBMC and analyzed with 10x Genomics Gene Expression Flex with Feature Barcodes and Multiplexing kit with Fix-Stain protocol.

G65109-1-5C was used to stain PBMC under 4hr LPS + TI treatment and analyzed with 10x Genomics Gene Expression Flex with Feature Barcodes and Multiplexing kit with Fix-Stain protocol.

G65109-1-5C was used to stain Resting PBMC and analyzed with 10x Genomics Gene Expression Flex with Feature Barcodes and Multiplexing kit with Stain-Fix protocol.

G65109-1-5C was used to stain PBMC under 4hr LPS + TI treatment and analyzed with 10x Genomics Gene Expression Flex with Feature Barcodes and Multiplexing kit with Stain-Fix protocol.

G65226-1-5C was used to stain Resting PBMC and analyzed with 10x Genomics Gene Expression Flex with Feature Barcodes and Multiplexing kit with Fix-Stain protocol.

G65226-1-5C was used to stain PBMC under 4hr LPS + TI treatment and analyzed with 10x Genomics Gene Expression Flex with Feature Barcodes and Multiplexing kit with Fix-Stain protocol.

G65226-1-5C was used to stain Resting PBMC and analyzed with 10x Genomics Gene Expression Flex with Feature Barcodes and Multiplexing kit with Stain-Fix protocol.

G65226-1-5C was used to stain PBMC under 4hr LPS + TI treatment and analyzed with 10x Genomics Gene Expression Flex with Feature Barcodes and Multiplexing kit with Stain-Fix protocol.

Various lysates were subjected to SDS PAGE followed by western blot with 20103-1-AP (CD45 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours.

Immunohistochemical analysis of paraffin-embedded human colon tissue slide using 20103-1-AP (CD45 antibody) at dilution of 1:4000 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

Immunohistochemical analysis of paraffin-embedded human colon tissue slide using 20103-1-AP (CD45 antibody) at dilution of 1:4000 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

Immunofluorescent analysis of (4% PFA) fixed human tonsillitis tissue using CD45 antibody (20103-1-AP) at dilution of 1:200 and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L).

Immunofluorescent analysis of (4% PFA) fixed human tonsillitis tissue using CD45 antibody (20103-1-AP) at dilution of 1:200 and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L).

IP result of anti-CD45 (IP:20103-1-AP, 4ug; Detection:20103-1-AP 1:300) with mouse spleen tissue lysate 4800ug.

1X10^6 Jurkat cells were stained with 0.5ug CD45 antibody (20103-1-AP, red) and control antibody (blue). Fixed with 90% MeOH blocked with 3% BSA (30 min). Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L) with dilution 1:1000.

1X10^6 human PBMCs were surface stained with 5 ul FITC Anti-Human CD45 (FITC-65109, Clone:HI30) (red) or Mouse IgG1 Isotype Control. Cells were not fixed. Lymphocytes were gated.

1X10^6 human PBMCs were surface stained with 10 ul APC Anti-Human CD45 (APC-65064, Clone: F10-89-4) or Mouse IgG2a Isotype Control. Cells were not fixed. Lymphocytes were gated.

1X10^6 human PBMCs were surface stained with 10 ul APC Anti-Human CD45 (APC-65064, Clone: F10-89-4) or Mouse IgG2a Isotype Control. Cells were not fixed. Lymphocytes were gated.