Anti-FCRL1+FCRL2 antibody [EPR26947-62] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal FCRL2 antibody. Carrier free. Suitable for Flow Cyt, Flow Cyt (Intra) and reacts with Human, Transfected cell line - Human samples.
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CD307b, FCRH2, IFGP4, IRTA4, SPAP1, UNQ9236/PRO31998, FCRL2, Fc receptor-like protein 2, FcR-like protein 2, FcRL2, Fc receptor homolog 2, IFGP family protein 4, Immunoglobulin receptor translocation-associated protein 4, SH2 domain-containing phosphatase anchor protein 1, FcRH2, CD307a, FCRH1, IFGP1, IRTA5, FCRL1, Fc receptor-like protein 1, FcR-like protein 1, FcRL1, Fc receptor homolog 1, IFGP family protein 1, Immune receptor translocation-associated protein 5, FcRH1, hIFGP1
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-FCRL1+FCRL2 antibody [EPR26947-62] - BSA and Azide free (AB308065)
This data was developed using ab308064, the same antibody clone in a different buffer formulation. Flow cytometric analysis of 2% paraformaldehyde fixed 0.1% Tween-20 permeabilized HEK-293T cells transfected with Myc-tagged FCRL3 overexpression construct / HEK-293T cells transfected with Myc-tagged FCRL4 overexpression construct / HEK-293T cells transfected with Myc-tagged FCRL5 overexpression construct cells labelling FCRL1+FCRL2 with ab308064 at 1/50 dilution (1ug), compared with a Rabbit monoclonal IgG (ab172730) isotype control (left). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody. Cells were surface stained with ab308064, then fixed with 2% PFA for 10 min followed by intracellularly staining with anti-Myc tag conjugated to Alexa Fluor® 647.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-FCRL1+FCRL2 antibody [EPR26947-62] - BSA and Azide free (AB308065)
This data was developed using ab308064, the same antibody clone in a different buffer formulation. Flow cytometric analysis of human PBMC (human peripheral blood mononuclear cell) cells labelling FCRL1+FCRL2 with ab308064 at 1/50 dilution (1ug)/ Right compared with a Rabbit monoclonal IgG (ab172730) isotype control / Left. Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody. Cells were stained with rabbit IgG or ab308064, then co-stained with anti-CD19 conjugated to Alexa Fluor® 647. Gated on viable cells.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-FCRL1+FCRL2 antibody [EPR26947-62] - BSA and Azide free (AB308065)
This data was developed using ab308064, the same antibody clone in a different buffer formulation. Flow cytometric analysis of 2% paraformaldehyde fixed 0.1% Tween-20 permeabilized HEK-293T cells transfected with Myc-tagged FCRL1 overexpression construct (Middle) and HEK-293T cells transfected with Myc-tagged FCRL2 overexpression construct (Right) cells labelling FCRL1+FCRL2 with ab308064 at 1/50 dilution (1ug), compared with a Rabbit monoclonal IgG (ab172730) isotype control (Left). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody. Cells were surface stained with ab308064, then fixed with 2% PFA for 10 min followed by intracellularly staining with anti-Myc tag conjugated to Alexa Fluor® 647.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-FCRL1+FCRL2 antibody [EPR26947-62] - BSA and Azide free (AB308065)
This data was developed using ab308064, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 2% paraformaldehyde fixed 0.1% Tween-20 permeabilized HEK-293T cells transfected with Myc-tagged FCRL3 overexpression construct / HEK-293T cells transfected with Myc-tagged FCRL4 overexpression construct / HEK-293T cells transfected with Myc-tagged FCRL5 overexpression construct cells labelling FCRL1+FCRL2 with ab308064 at 1/50 dilution (1ug), compared with a Rabbit monoclonal IgG (ab172730) isotype control (left).
A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Cells were surface stained with ab308064, then fixed with 2% PFA for 10 min followed by intracellularly staining with anti-Myc tag conjugated to Alexa Fluor® 647.
Related conjugates and formulations (1)
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Anti-FCRL1+FCRL2 antibody [EPR26947-62]
Reactivity data
Product details
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.
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
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
These proteins are integral to immune function. FCRL1 participates in the regulation of B cell activation and antibody production while FCRL2 modulates B cell responses during immune processes. Both proteins can interact with various immunoglobulins suggesting their role in modulating signaling pathways associated with B cell receptor activity. FCRL1 and FCRL2 appear to be components of larger regulatory complexes on the B cell surface coordinating immune response based on extracellular signals.
Pathways
FCRL1 and FCRL2 are involved in B cell signaling networks. They form important components of pathways like the B cell receptor (BCR) signaling and the immune regulation network. Both proteins are associated with other receptor proteins such as CD19 and CD21 playing a part in fine-tuning the signaling processes that influence B cell maturation and antibody responses. Their activity influences not just BCR signaling but also other related immune regulatory pathways bridging external signals and B cell functionality.
Product protocols
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Target data
Additional targets
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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