LIRA1 Polyclonal Antibody, 20ul Enzymes but the full-length nature of

but the full-length nature of many of these variants has not been determined

This gene encodes a homeobox-containing transcription factor

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Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency

The protein encoded by this gene is localized to the cytoplasmic face of the nuclear pore complex where it is required for proper cell cycle progression and nucleocytoplasmic transport

LIRA1 Polyclonal Antibody, 20ul Enzymes but the full-length nature ofThis gene encodes an activating member of the leukocyte immunoglobulin like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13. 4. The encoded protein is predominantly expressed in B cells, interacts with major histocompatibility complex class I ligands, and contributes to the regulation of immune responses. Alternative splicing results in multiple transcript variants encoding different isoforms.