Anti-CD15 antibody [SP159] - BSA and Azide free
- BOND RX™ Validated
- Advanced Validation
- RabMAb
- Recombinant
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(1 Review)
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(1 Publication)
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human spleen tissue sections labeling CD15 with ab135377 at 1/50 dilution (3.14 μg/ml). Heat mediated antigen retrieval with Bond™ Epitope Retrieval Solution 2 (pH 9.0) for 10mins. Goat Anti-Rabbit & Mouse IgG (HRP) was used as the secondary antibody. Hematoxylin was used as a counterstain. Positive staining on the human spleen, performed on a Leica Biosystems BOND™ RX instrument.
The section was incubated with ab135377 for 30 mins at room temperature. This image was generated using ab135377, the same clone, but with a different buffer formulation.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human Hodgkin's lymphoma tissue sections labeling CD15 with ab135377 at 1/50 dilution (3.14 μg/ml). Heat mediated antigen retrieval with Bond™ Epitope Retrieval Solution 2 (pH 9.0) for 10mins. Goat Anti-Rabbit & Mouse IgG (HRP) was used as the secondary antibody. Hematoxylin was used as a counterstain. Positive staining on the human Hodgkin's lymphoma, performed on a Leica Biosystems BOND™ RX instrument.
The section was incubated with ab135377 for 30 mins at room temperature. This image was generated using ab135377, the same clone, but with a different buffer formulation.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
Immunohistochemical analysis of formalin-fixed, paraffin-embedded human Hodgkin's Lymphoma tissue labelling CD15 with ab135377 at 1/100 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA and sodium azide (ab135377).
- Flow Cyt
Unknown
Flow Cytometry - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
Flow cytometry analysis of THP-1 (human acute monocytic leukemia) labeling CD15 with purified ab135377 at 1/20 dilution (7.85 μg/ml) (red). Goat anti rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as a secondary antibody. Isotypecontrol - Rabbit monoclonal IgG (ab172730) (black). Unlableled control - Unlabelled cells (blue).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab135377).
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
Flow cytometric analysis of rabbit anti-CD15 (SP159) antibody ab135377 (1/200) in HL-60 cells(green) compared to negative control of rabbit IgG (blue).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab135377).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human cervix carcinoma tissue sections labeling CD15 with ab135377 at 1/50 dilution (3.14 μg/ml). Heat mediated antigen retrieval with Bond™ Epitope Retrieval Solution 2 (pH 9.0) for 10mins. Goat Anti-Rabbit & Mouse IgG (HRP) was used as the secondary antibody. Hematoxylin was used as a counterstain. Positive staining on the human cervix carcinoma, performed on a Leica Biosystems BOND™ RX instrument.
The section was incubated with ab135377 for 30 mins at room temperature. This image was generated using ab135377, the same clone, but with a different buffer formulation.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
This data was developed using ab135377, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human spleen tissue staining CD15 with ab135377 at a 1/50 dilution and ab272713 anti-S100A12/CGRP used at 1/5000 dilution. Opal Polymer HRP Ms + Rb was used as a secondary, and DAPI was used for a nuclear counter stain. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Panel A : merged staining of anti-CD15 (green; Opal™520), anti-S100A12/CGRP (magenta; Opal™690) on human spleen.
Panel B : anti-CD15 stained granulocytes and monocytes on human spleen.
Panel C : anti-S100A12/CGRP stained neutrophils and monocytes on human spleen.
Panel D : Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab135377 and ab272713 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
This data was developed using ab135377, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human Hodgkin's lymphoma tissue staining CD15 with ab135377 at a 1/50 dilution and ab272713 anti-S100A12/CGRP used at 1/5000 dilution. Opal Polymer HRP Ms + Rb was used as a secondary, and DAPI was used for a nuclear counter stain. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Panel A : merged staining of anti-CD15 (green; Opal™520) and anti-S100A12/CGRP (magenta; Opal™690) on human Hodgkin's lymphoma.
Panel B : anti-CD15 stained granulocytes and monocytes on human Hodgkin's lymphoma.
Panel C : anti-S100A12/CGRP stained neutrophils and monocytes on human Hodgkin's lymphoma.
Panel D : Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab135377 and ab272713 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
- Flow Cyt
Lab
Flow Cytometry - Anti-CD15 antibody [SP159] - BSA and Azide free (AB240092)
This data was developed using ab135377, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of human neutrophils cells labelling CD15 with ab135377 at 1/2000 compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Goat Anti-Rabbit IgG (Alexa Fluor® 488 (ab150081) at 1/5000 was used as the secondary antibody.
Gated on viable cells.
Related conjugates and formulations (4)
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Anti-CD15 antibody [SP159]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-CD15 antibody [SP159]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-CD15 antibody [SP159]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-CD15 antibody [SP159]
Reactivity data
Product details
ab240092 is the carrier-free version of ab135377.
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.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Purification notes
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
CD15 is important in cell-cell interaction mechanisms. It plays a role in mediating adhesion processes particularly in immune responses where it aids neutrophils in adhering to vascular endothelium and transmigrating to sites of infection or inflammation. As a glycoconjugate CD15 forms part of a larger glycoprotein complex on the cell surface interacting with other proteins to facilitate cellular responses and movement.
Pathways
CD15's function as an adhesion molecule ties into key cellular processes such as the selectin pathway. In this pathway it interacts with proteins like E-selectin and L-selectin contributing to leukocyte rolling and extravasation during the immune response. Additionally CD15 is implicated in the signaling pathways that mediate inflammatory responses where its role in neutrophil dynamics is important.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Oncology reports 46: PubMed34528699
2021
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'.
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