ADCYA Rabbit Polyclonal Antibody, 50ul Plasma The chromosome 22 breakpoint for

The chromosome 22 breakpoint for this translocation is located within the BCR gene (BCR

Mutations in PEX10 result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders

peptides from the C-terminal region of the protein have antimicrobial activity against bacterial pathoge

The encoded protein possesses a unique extracellular region that contains two immunoglobulin-like domains| three epidermal growth factor (EGF)-like domains and three fibronectin type III repeats

ADCYA Rabbit Polyclonal Antibody, 50ul Plasma The chromosome 22 breakpoint forThe protein encoded by this gene belongs to a distinct class of adenylyl cyclases that is soluble and insensitive to G protein or forskolin regulation. Activity of this protein is regulated by bicarbonate. Variation at this gene has been observed in patients with absorptive hypercalciuria. Alternatively spliced transcript variants encoding different isoforms have been observed. There is a pseudogene of this gene on chromosome 6.