CD57 Polyclonal Antibody, 100ul[BT-AP02282] Enzyme-Linked Immunosorbent Assay (ELISA) Defects in this gene cause

Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency

The alpha subunits are of 2 types: those that are functional by themselves and those that are electrically silent but capable of modulating the activity of specific functional alpha subunits

Several transcript variants encoding different isoforms of supervillin have been described

Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex

CD57 Polyclonal Antibody, 100ul[BT-AP02282] Enzyme-Linked Immunosorbent Assay (ELISA) Defects in this gene causeCysteine and serine rich nuclear protein 2 encoded by CSRNP2 belongs to the CSRNP family of nuclear proteins that share conserved regions, including cysteine and serine rich regions, a basic domain, a transcriptional activation domain, and bind the sequence 'AGAGTG', thus have the hallmark of transcription factors. Studies in mice suggest that these genes may have redundant functions. Alternatively spliced transcript variants have been found for