Anti-CD72 antibody - N-terminal
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(1 Publication)
Rabbit Polyclonal CD72 antibody. N-terminal. Suitable for IHC-P and reacts with Human samples. Cited in 1 publication. Immunogen corresponding to Synthetic Peptide within Human CD72 aa 1-50 conjugated to Keyhole Limpet Haemocyanin.
View Alternative Names
CD72, B-cell differentiation antigen CD72, Lyb-2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD72 antibody - N-terminal (AB202843)
Immunohistochemical analysis of formalin-fixed, paraffin-embedded Human gastric carcinoma tissue labeling CD72 with ab202843 at 1/200 dilution, followed by conjugation to the secondary antibody and DAB staining.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD72 antibody - N-terminal (AB202843)
Immunohistochemical analysis of formalin-fixed, paraffin-embedded Human cervical carcinoma tissue labeling CD72 with ab202843 at 1/200 dilution, followed by conjugation to the secondary antibody and DAB staining.
Reactivity data
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Biological function summary
CD72 functions as a regulatory protein that influences B cell activity by modulating BCR signaling thresholds. CD72 is part of receptor-ligand complexes on the B cell surface. It operates alongside other proteins like CD5 and SHP-1 to fine-tune immune responses. By interacting with these proteins CD72 helps in maintaining immune balance and prevents overactivation that can lead to autoimmune reactions. This protein modulates both positive and negative signaling affecting B cell survival and differentiation.
Pathways
CD72 influences immune response pathways specifically the BCR signaling pathway and the downstream PI3K-Akt pathway. As a negative regulator CD72 works in tandem with proteins such as Lyn and SHP-1 to attenuate BCR signal transduction. These signaling cascades play a role in immune responses lymphocyte development and adaptation. The involvement of CD72 in these pathways illustrates its function in balancing the intensity of signals received by B cells ultimately affecting immune response outcomes.
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Publications (1)
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Cardiovascular research 118:1303-1320 PubMed34100920
2021
Applications
Unspecified application
Species
Unspecified reactive species
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