IFNGR2 Rabbit pAb
This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disorder (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disorder with autosomal recessive, autosomal dominant or X-linked inheritance.
Internal Reference:
antibody-sk9560
Size:
1000uL