• Official Full Name
  • DnaJ (Hsp40) homolog, subfamily C, member 30
  • Background
  • This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
  • Synonyms
  • DNAJC30; DnaJ (Hsp40) homolog, subfamily C, member 30; WBSCR18, Williams Beuren syndrome chromosome region 18; dnaJ homolog subfamily C member 30; DNAJC 30; WBSCR18; DnaJ (Hsp40) homolog subfamily C member 30; MGC12943; WBSCR 18; Williams Beuren syndrome chromosomal region 18 protein; Williams Beuren syndrome chromosome region 18; williams-Beuren syndrome chromosomal region 18 protein
Source (Host):Wheat GermSpecies:Human
Product nameRecombinant Human DNAJC30 Protein, GST-tagged
Source (Host):E. coliSpecies:Human
Product nameRecombinant Human DNAJC30, His tagged
Source (Host):Mammalian CellsSpecies:Mouse
Product nameRecombinant Mouse DNAJC30 Protein
Source (Host):Mammalian CellsSpecies:Rhesus Macaque
Product nameRecombinant Rhesus monkey DNAJC30 Protein, His-tagged
Source (Host):Species:Human
Product nameRecombinant Human DNAJC30 293 Cell Lysate

Interacting Protein

DNAJC30 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with DNAJC30 here. Most of them are supplied by our site. Hope this information will be useful for your research of DNAJC30.