LIR-7 Polyclonal Antibody, 20ul[BT-AP05032] Primary Antibodies Defects in this gene are

Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2)

to induce either leukocyte adhesion and migration or chemotactic functions

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Multiple alternatively spliced transcript variants have been found for CTSL

LIR-7 Polyclonal Antibody, 20ul[BT-AP05032] Primary Antibodies Defects in this gene areLILRA2 encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. Leukocyte immunoglobulin like receptor subfamily A member 2 is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been