APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control
- RabMAb
- Recombinant
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- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CD62L with ab317478 at 1/5000 dilution (0.01ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control.
Cells were stained with anti-CD4 conjugated to Alexa Fluor® 488. Gated on viable lymphocytes.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing left THP-1 positive cells and right negative HCT116 stained with ab315146 (red line). The cells were fixed with 4% formaldehyde (10 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10μg/ml human IgG and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab315146) (1x 106in 100μl at 0.2μg/ml (1/2500)) for 30min at 22°C.
Isotype control antibody (black line) was APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control used at the same concentration and conditions as the primary antibody. Unlabelled sample (blue line) was also used as a control.
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling IL-10RA with ab325784 at 1/500 dilution (0.1ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Cells were co-stained with CD14 conjugated to Brilliant Violet 421. Gated on viable cells.
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling IL-10RA with ab325784 at 1/500 dilution (0.1ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Cells were co-stained with CD4 conjugated to Alexa Fluor®488. Gated on viable lymphocyte.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing left K-562 positive cells and right negative A549 stained with ab314948 (red line). The cells were fixed with 4% formaldehyde (10 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10μg/ml human IgG and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab314948) (1x 106in 100μl at 0.04μg/ml (1/12500)) for 30min at 22°C.
Isotype control antibody (black line) was APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control used at the same concentration and conditions as the primary antibody. Unlabelled sample (blue line) was also used as a control.
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Wild-type HeLa (human cervix adenocarcinoma epithelial cell, Right) / SLC3A2 (CD98) knockout HeLa (Left) cells labelling CD98 with ab317481 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CD62L with ab317478 at 1/5000 dilution (0.01ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control.
Gated on viable cells.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Jurkat (human T cell leukemia T lymphocyte from peripheral blood, Left) / Raji (human Burkitt's lymphoma B lymphocyte, Right) cells labelling CD19 with ab317484 at 1/5000 dilution (0.01ug) (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Negative control : Jurkat (PMID : 19147785)
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HeLa(human cervical adenocarcinoma epithelial cell) cells labelling beta Tubulin with ab317754 at 1/500 dilution(0.1ug)/Red (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry staining of human peripheral blood mononuclear cells (PBMCs) with ab314955 (right) or APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (left). PBMCs were incubated for 30 min on ice in 1x PBS containing 10 μg/ml human IgG and 10 % normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody ab314955 or APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (1x 106in 100 μl at 1.0 μg/ml (1/500)) for 30min on ice. The cells were simultaneously stained with CD11b.
Acquisition of >30000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter. Events were gated on viable cells.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing left Jurkat positive cells and right negative Hela stained with ab314938 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10% normal goat serum to block non-specific protein-protein interaction followed by the antibody (ab314938) (1x 106in 100μl at 0.04μg/ml (1/12500)) for 30min at 22°C.
Isotype control antibody (black line) was APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control used at the same concentration and conditions as the primary antibody. Unlabelled sample (blue line) was also used as a control.
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of HEK-293 (human embryonic kidney epithelial cell, Left) / Huh7 (human hepatocellular carcinoma epithelial cell, Right) cells labelling LDL Receptor with ab322128 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Low expression : HEK-293.
Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CLEC4A with ab322023 at 1/5000 dilution (0.01ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Gated on viable cells. Cells are co-stained with CD11b conjugated to Brilliant Violet 421.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CLEC4A with ab322023 at 1/5000 dilution (0.01ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Gated on viable cells.
Cells are co-stained with CD3 conjugated to Alexa Fluor®488.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing wild-type A549 (green line) and GLUT1 knockout A549 stained with ab316298 (magenta line). The cells were fixed with 4% formaldehyde (10 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10μg/ml human IgG and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab316298) (1x 10E6 in 100μl at 0.04 μg/ml (1/12500)) for 30min at 22°C.
Isotype control antibody APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab232814) was used at the same concentration and conditions as the primary antibody (wild-type A549 - black line, GLUT1 knockout A549 - grey line). Unlabelled sample was also used as a control (this line is not shown for the purpose of simplicity).
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HeLa (human cervical adenocarcinoma epithelial cell) cells labelling GRP94 with ab317477 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of LNCaP (human prostate carcinoma epithelial cell, Left) / PC-3 (human prostate adenocarcinoma epithelial cell, Right) cells labelling LDL Receptor with ab322128 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Low expression : LNCaP.
Gated on viable cells.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized MOLT-4 (human lymphoblastic leukemia T lymphoblast, Left) / Ramos (human Burkitt's lymphoma B lymphocyte, Right) cells labelling BTK with ab317755 at 1/100000 dilution(0.0005ug)/Red (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Negative control : MOLT-4 (PMID : 24759210)
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing wild-type Jurkat (green line) and IDH2 knockout Jurkat stained with ab317932 (magenta line). The cells were fixed with 80% methanol (5 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10% normal goat serum to block non-specific protein-protein interaction followed by the antibody (ab317932) (1x 106 in 100μl at 0.008 μg/ml (1/62500)) for 30min at 22°C.
Isotype control antibody was APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control in Jurkat WT cells (black line) and Jurkat-IDH2 KO cells (grey line), used at the same concentration and conditions as the primary antibody.
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling IL-10RA with ab325784 at 1/500 dilution (0.1ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Cells were co-stained with CD56 conjugated to Brilliant Violet 421. Gated on viable lymphocyte.
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CD300a with ab325381 at 1/500 dilution (0.1ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Gated on viable cells. Cells were co-stained with anti human CD14 conjugated to Brilliant Violet 421.
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CD300a with ab325381 at 1/500 dilution (0.1ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Gated on viable cells. Cells were co-stained with anti human CD19 conjugated to PE/CY7.
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry staining of human peripheral blood mononuclear cells (PBMCs) with ab314954 (right) or APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (left). PBMCs were incubated for 30 min on ice in 1x PBS containing 10 μg/ml human IgG and 10 % normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody ab314954 or APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (1x 106in 100 μl at 0.2 μg/ml (1/2500)) for 30min on ice. The cells were simultaneously stained with CD56.
Acquisition of >30000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter. Events were gated on viable lymphocytes.
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry staining of human peripheral blood mononuclear cells (PBMCs) with ab306538 (right) or Rabbit IgG (monoclonal) Allophycocyanin (ab232814) isotype (left). PBMCs were incubated for 30 min on ice in 1x PBS containing 10μg/ml human IgG and 10%; normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab306538) or Rabbit IgG (monoclonal) Allophycocyanin (ab232814) isotype (100 μl at 0.04μg/ml (1/12500)) for 30 min on ice. The cells were simultaneously stained with CD19.
Acquisition of >30000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter. Events were gated on live lymphocytes.
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 293T (human embryonic kidney epithelial cell, Left) THP-1 (human monocytic leukemia monocyte, Right) cells labelling CD300a with ab325381 at 1/500 dilution (0.1ug) / Red compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Black isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Gated on viable cells. Negative control : 293T (PMID : 22043923)
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing wild-type HAP1 (green line) and HMGB1 knockout HAP1 stained with ab225041(magenta line). The cells were fixed with 4% formaldehyde (10 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10μg/ml human IgG and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab225041) (1x 10E6 in 100μl at 0.04 μg/ml (1/12500) for 30min at 22°C.
Isotype control antibody APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab232814) was used at the same concentration and conditions as the primary antibody (wild-type HAP1 - black line, HMGB1 knockout HAP1 - grey line). Unlabelled sample was also used as a control (this line is not shown for the purpose of simplicity).
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 2% paraformaldehyde fixed 0.1% Tween-20 permeabilized Isotype (Left) / HEK-293T (human embryonic kidney) cells transfected with a human SIGLEC8 expression vector containing a myc-his tag (Middle) / 293T transfected with an empty vector containing a myc-His tag (Right) cells labelling SIGLEC8 with ab318168 at 1/5000 dilution (0.01ug) / Middle and Right (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Live cells were surface stained with ab318168, then fixed with 2% PFA followed by intracellular staining with Myc-tag conjugated to Alexa Fluor® 488.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of SH-SY5Y (human neuroblastoma epithelial cell, Left) / HeLa (human cervix adenocarcinoma epithelial cell, Right) cells labelling CD98 with ab317481 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Gated on viable cells. Low expression : SH-SY5Y .
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing wild-type Raji (green line) and CXCR5 knockout Raji stained with ab316179 (red line). The cells were incubated in 1x PBS containing 10μg/ml human IgG and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab316179) (1x 106 in 100μl at 0.04 μg/ml (1/12500)) for 30min on ice.
Isotype control antibody APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab232814) was used at the same concentration and conditions as the primary antibody (wild-type Raji - black line, CXCR5 knockout Raji - grey line). Unlabelled sample was also used as a control (this line is not shown for the purpose of simplicity).
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Isotype (Left) / HEK-293T (human embryonic kidney epithelial cell) transfected with a CBX1-V5-tagged expression vector containing a myc tag (Middle) / 293T transfected with an empty vector containing a myc-His tag (Right) cells labelling V5 tag with ab317483 at 1/5000 dilution (0.01ug) / Middle and Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing HeLa cells stained with ab316299 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were incubated in 1x PBS containing 10μg/ml human IgG and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab316299) (1x 10E6 in 100μl at 0.04μg/ml (1/12500)) for 30min at 22°C.
Isotype control antibody (black line) APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab232814) was used at the same concentration and conditions as the primary antibody. Unlabelled sample (blue line) was also used as a control.
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
This antibody gave a positive signal in HeLa Fixed with 4% formaldehyde (10 min) / permeabilised with 0.1% PBS-Triton X-100 for 15 min under the same conditions.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Isotype (Left) / 293T (human embryonic kidney epithelial cell) cells transfected with a mouse C1QA expression vector containing a Myc tag(Middle) / 293T cells containing a Myc tag (Right) cells labelling 6X His tag with ab317659 at 1/5000 dilution(0.01ug) / Middle and Right (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry overlay histogram showing wild-type HAP1 (green line) and SMARCA4 knockout HAP1 stained with ab314953 (red line). The cells were fixed with 4% formaldehyde (10 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10% normal goat serum to block non-specific protein-protein interaction followed by the antibody (ab314953) (1x 106in 100μl at 0.04 μg/ml (1/12500)) for 30min at 22°C.
Isotype control antibody APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control was used at the same concentration and conditions as the primary antibody (wild-type HAP1 - black line, SMARCA4 knockout HAP1 - grey line). Unlabelled sample was also used as a control (this line is not shown for the purpose of simplicity).
Acquisition of >5000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter.
This antibody gave a positive signal in HAP1 Fixed with 80% methanol (5 min) / permeabilised with 0.1% PBS-Triton X-100 for 15 min under the same conditions.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Human PBMC (human peripheral blood mononuclear cell) cells labelling CD62L with ab317478 at 1/5000 dilution (0.01ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype contro.
Cells were stained with anti-CD4 conjugated to Alexa Fluor® 488 and anti-CD45RO (BV421). Gated on viable CD4+ T cells.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Isotype (Left) / Mouse bone marrow treated with 2ug/ml LPS for 24h (Middle) / Untreated mouse bone marrow (Right) cells labelling CD204 with ab320786 at 1/500 dilution (0.1ug) / Middle and Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Cells are co-stained with F4/80 conjugated with PE.
Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of Mouse bone marrow cells cells labelling Sialoadhesin/CD169 with ab317480 at 1/5000 dilution (0.01ug) / Right compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) / Left isotype control.
Gated on viable cell. Mouse bone marrow cells are co-stained with F4/80 conjugated PE.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HL-1 (mouse atrial muscle cell) cells labelling Cardiac Troponin T with ab317475 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit IgG monoclonal [EPR25A] - Isotype Control (Allophycocyanin) (ab232814) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
- Flow Cyt
Lab
Flow Cytometry - APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (AB232814)
Flow cytometry staining of C57 BL/6 mouse splenocytes with ab315142 (right) or APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (left). Cells were incubated for 30 min on ice in 1x PBS containing 10μg/ml anti CD16/CD32 and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody ab315142 or APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (1x 106in 100 μl at 1.0 μg/ml (1/500)) for 30min on ice. The cells were simultaneously stained with c-Kit.
Acquisition of >30000 events were collected using a 40 mW Red laser (638nm) and 660/10 bandpass filter. Events were gated on viable cells.
Related conjugates and formulations (15)
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519 FITC
FITC Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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675 PerCP
PerCP Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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578 PE
PE Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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603 Alexa Fluor® 568
Alexa Fluor® 568 Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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617 Alexa Fluor® 594
Alexa Fluor® 594 Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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519 Alexa Fluor® 488
Alexa Fluor® 488 Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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HRP Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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665 Alexa Fluor® 647
Alexa Fluor® 647 Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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421 Alexa Fluor® 405
Alexa Fluor® 405 Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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565 Alexa Fluor® 555
Alexa Fluor® 555 Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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Biotin Isotype Control [EPR25A]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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Rabbit IgG, monoclonal [EPR25A] - Isotype Control
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Rabbit IgG, monoclonal [EPR25A] - Isotype Control - BSA and Azide Free
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Rabbit IgG, monoclonal [EPR25A] - Isotype Control (Low endotoxin, Azide free)
Reactivity data
Product details
What is this antibody validated in?
APC Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab232814) is a rabbit recombinant monoclonal antibody and is validated for use in Flow Cytometry (Intra), Flow Cytometry (Flow Cyt).
Other related products
We have a range of other formats of antibody clone [EPR25A] also available for your convenience: ab172730, Alexa Fluor® 488 - ab199091, Alexa Fluor® 647 - ab199093, Carrier free - ab199376, HRP - ab199507, Alexa Fluor® 405 - ab208150, Alexa Fluor® 594 - ab208568, Alexa Fluor® 555 - ab208569, PE - ab209478, Alexa Fluor® 568 - ab209613, Carrier free - ab210849, PerCP - ab222107, FITC - ab223339, APC - ab232814, Biotin - ab320073, Alexa Fluor® 750 - ab322086
Immunogen
Chemical / Small Molecule conjugated to keyhole limpet haemocyanin. KLH is a copper containing oxygen carrier occurring freely dissolved in the hemolymph of many molluscs and arthropods. KLH forms a large complex composed of ~50 kDa subunits.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (2)
Recent publications for all applications. Explore the full list and refine your search
Cancers 16: PubMed39335098
2024
Applications
Unspecified application
Species
Unspecified reactive species
eLife 9: PubMed32697192
2020
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com