||Recombinant fragment, corresponding to amino acids 25 - 91 of Human IGF2, 7505 Dalton.
||This gene encodes a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumour, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. A read-through INS-IGF2 gene exists, whose 5 region overlaps the INS gene and the 3 region overlaps this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
||Lyophilised:Reconstitute in sterile 18MO-cm H2O at a concentration of 100μg/ml, which can then be further diluted to other aqueous solutions.
||>95% by SDS-PAGE
||Preservative: NoneConstituents: 1X PBS
||Aliquot and store at -80°C. Avoid repeated freeze / thaw cycles.
|Sequences of amino acids:
||AYRPSETLCG GELVDTLQFV CGDRGFYFSR PASRVSRRSR GIVEECCFRS CDLALLETYC ATPAKSE
||Belongs to the insulin family.