FHR5 Rabbit Polyclonal Antibody, 20ul Oligo Pool and in a rare syndrome

and in a rare syndrome known as alternating hemiplegia of childhood

such as ELOVL6

Transcripts for this gene undergo alternative splicing that results in many tissue-specific isoforms

Mutations in DOK7 are a cause of familial limb-girdle myasthenia autosomal recessive

This protein forms a very tight complex with alpha neurexins

FHR5 Rabbit Polyclonal Antibody, 20ul Oligo Pool and in a rare syndromeThis gene is a member of a small complement factor H (CFH) gene cluster on chromosome 1. Each member of this gene family contains multiple short consensus repeats (SCRs) typical of regulators of complement activation. The protein encoded by this gene has nine SCRs with the first two repeats having heparin binding properties a region within repeats 5 7 having heparin binding and C reactive protein binding properties and the C terminal repeats being