C16orf57 (USB1) Mouse Monoclonal Antibody [Kloon ID: LBI1B1]

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. [provided by RefSeq, Mar 2011]

Carrier-free (BSA/glycerol-free) C16orf57 mouse monoclonal antibody, clone LBI1B1

C16orf57; hUsb1; HVSL1; Mpn1; PN

Homo sapiens U6 snRNA biogenesis phosphodiesterase 1 (USB1), transcript variant 1, mRNA.

79650

Q9BQ65

Unconjugated

WB 1:500~2000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

USB1

https://www.ncbi.nlm.nih.gov/gene/?term=79650

https://www.uniprot.org/uniprot/Q9BQ65