General description
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. (provided by RefSeq)
Immunogen
WBSCR18 (AAH05056, 1 a.a. ~ 226 a.a) full-length human protein.
Sequence
MAAMRWRWWQRLLPWRLLQARGFPQNSAPSLGLRARTYSQGDCSYSRTALYDLLGVPSTATQAQIKAAYYRQCFLYHPDRNSGSAEAAERFTRISQAYVVLGSATLRRKYDRGLLSDEDLRGPGVRPSRTPAPDPGSPRTPPPTSRTHDGSRASPGANRTMFNFDAFYQAHYGEQLERERRLRARREALRKRQEYRSMKGLRWEDTRDTAAIFLIFSIFIIIGFYI
Physical form
Solution in phosphate buffered saline, pH 7.4
- UPC:
- 41105328
- Condition:
- New
- Availability:
- 3-5 Days
- Weight:
- 1.00 Ounces
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- SAB1409888-50UG
- Product Size:
- 50/µG