BT3A1 Polyclonal Antibody, 50ul Immunoassays It is a C-type lectin

It is a C-type lectin with mannose binding specificity

Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype

1-10μl volumes

This gene encodes a phosphorylated protein that is a member of a Skp1-Cullin-F-box-like complex

consisting of two alpha and four beta subunits

BT3A1 Polyclonal Antibody, 50ul Immunoassays It is a C-type lectinThe butyrophilin (BTN) genes are a group of major histocompatibility complex (MHC) associated genes that encode type I membrane proteins with 2 extracellular immunoglobulin (Ig) domains and an intracellular B30. 2 (PRYSPRY) domain. Three subfamilies of human BTN genes are located in the MHC class I region: the single copy BTN1A1 gene (MIM 601610) and the BTN2 (e. g., BTN2A1; MIM 613590) and BTN3 (e. g., BNT3A1) genes, which have undergone tandem