Supplier:
Aviva Systems Biology IncorporatedC16orf57 (chromosome 16 open reading frame 57 ) Blocking Peptide (the C terminal of C16orf57)(100ug)
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SPECIFICATIONS
Size
100ug
Reactivities
Hum
Format
Lyophilized powder
Presku
AAP62380
Target
This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
Weight
29kDa
Gene Id
The peptide is characterized by mass spectroscopy
Alternative Names
FLJ13154; HVSL1; PN
SUPPLIER INFO
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