NBPF5 Polyclonal Antibody, 50ul Capsule Filter Alternative transcript variants encoding distinct

Alternative transcript variants encoding distinct isoforms have been described

Knockout studies in mice exhibit neural tube defects and defective cilia| and mutations in this gene are associated with neural tube defects in humans

immune-mediated inflammatory diseases and feeding regulation

This gene encodes a hydrolase that serves as an important role in cellular purine metabolism by acting primarily on inosine 5'-monophosphate and other purine nucleotides

This gene is a member of the EPO/TPO family and encodes a secreted| glycosylated cytokine composed of four alpha helical bundles

NBPF5 Polyclonal Antibody, 50ul Capsule Filter Alternative transcript variants encoding distinctNBPF5 (neuroblastoma breakpoint family member 5) is a 351 amino acid cytoplasmic protein that is expressed in medulla and brain and belongs to the NBPF family. NBPF5 contains one NBPF domain and is encoded by a gene that maps to human chromosome 1p13. Chromosome 1 spans 260 million base pairs, contains over 3000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease associated genes, including those that are