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CD22 is a transmembrane receptor and member of the sialic acid-binding immunoglobulin-type (Ig-type) lectin (SIGLEC) family.1,2 It is composed of N-terminal extracellular Ig-like variable (IgV) and Ig-like constant 2 (IgC2) domains, a membrane-spanning region, and an intracellular immunoreceptor tyrosine-based inhibitory motif (ITIM) domain. CD22 has two isoforms formed via alternative splicing, CD22β, which is the full-length form and contains six IgC2 domains, and CD22α, which lacks the third and fourth IgC2 domains. It is expressed in the cytosol of premature B cells and on the cell surface of resting and activated B lymphocytes but is not expressed in differentiated B cells.3 CD22 is an inhibitory receptor activated by binding of α2,6-linked sialic acid-containing molecules, such as glycoproteins, which stimulates phosphorylation of tyrosine in the ITIM domain, leading to recruitment of Src homology 2 domain-containing phosphatases (SHPs), including SHP-1, spleen tyrosine kinase (Syk), LYN, and PI3K.1,2 Knockout of Cd22 decreases IgG1 titers in mice immunized with OVA/alum and expression of human CD22 in Cd22 -/- mice rescues this phenotype.4 CD22 is overexpressed in cancer cells isolated from patients with hairy cell leukemia.3 Cayman’s CD22 Rabbit Monoclonal Antibody (Clone 340) can be used for ELISA and immunohistochemistry (IHC; paraffin) applications.
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1. CD22: A regulator of innate and adaptive B cell responses and autoimmunity. Front. Immunol. 9, 2235 (2018).
2. CD22, a B lymphocyte-
3. HD39 (B3), a B lineage-
4. Human CD22 inhibits murine B cell receptor activation in a human CD22 transgenic mouse model. J. Immunol. 199(9), 3116-3128 (2017).