NSUN5 Polyclonal Antibody

Background:
NOP2/Sun RNA methyltransferase family member 5(NSUN5) Homo sapiens This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013],

Immunogen: Synthesized peptide derived from human protein . at AA range: 320-400

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 47

GeneID: NSUN5 WBSCR20 WBSCR20A

Storage: -20°C/1 year

NOTE: For Research Use Only